ANALYSIS OF PERIODONTAL DISEASE IN ASSOCIATION WITH CORONARY
ARTERY DISEASE AND INFLAMMATORY MEDIATORS IN PATIENTS
UNDERGO...
ANALYSIS OF PERIODONTAL DISEASE IN ASSOCIATION WITH CORONARY
ARTERY DISEASE AND INFLAMMATORY MEDIATORS IN PATIENTS
UNDERGO...
ACKNOWLEDGEMENTS
I would like to thank Drs. Brian Mealey, Devang Patel, Thomas Oates, and David
Lasho for giving me the op...
ANALYSIS OF PERIODONTAL DISEASE IN ASSOCIATION WITH CORONARY
ARTERY DISEASE AND INFLAMMATORY MEDIATORS IN PATIENTS
UNDERGO...
factors contributing to the inflammatory component of atherogenesis is at the forefront
of preventive cardiology. Interleu...
recorded to determine the extent and severity of periodontitis. Correlations between
periodontal parameters, levels of inf...
TABLE OF CONTENTS
Page
Title ……………………………………………………………………………. i
Approval ………………………………………………………………………. ii
Acknowledgements ……...
viii
LIST OF TABLES
Page
Table 1 Summary Statistics ……………………………………................. 29
Table 2 Coronary Artery Disease Sta...
I. INTRODUCTION AND LITERATURE REVIEW
A. Periodontitis as an Inflammatory Disease
Periodontal disease is characterized as ...
periodontal status and subgingival periodontal pathogens, Noack and colleagues
identified significantly higher mean CRP le...
cytokines; IL-6, a pro-inflammatory cytokine involved in osteoclast formation and
plasma cell proliferation; IL-8, a pro-i...
chronic periodontitis patients had significantly higher levels of IL-1β and IL-12, while
IL-11 exhibited an inverse correl...
were harvested. Fibroblasts from diseased tissue were shown to have higher
constituitive expression of IL-6 and IL-8 compa...
reduce levels of inflammatory mediators and limit alveolar bone loss (Cirelli 2008).
Establishment of a cause-and-effect r...
In addition to targeting the classic risk factors in the treatment and prevention of
cardiovascular disease (CVD), investi...
complex chain of events leading to atherosclerosis and identifying potential therapeutic
targets remains the focus of ongo...
systemic infection (Kiechl 2001). Another notable observation was that the risk of
atherosclerosis tended to be higher in ...
from a local infection is well supported in periodontal literature, as cited in section A of
the literature review.
In ord...
periodontal therapy on endothelial dysfunction were analyzed in a randomized
controlled clinical trial (Tonetti 2007). One...
disease (Beck 2005); hence a strong relationship between periodontal and cardiovascular
disease cannot be readily establis...
Interleukin-18 (IL-18) is a pro-inflammatory cytokine and is a member of the
interleukin-1 superfamily. It is expressed in...
The association between IL-18 and periodontal disease has also been
investigated, albeit to a lesser extent than in the ca...
receptor CXCR6. Lipopolysaccharide has been shown to upregulate CXCR6, the
receptor for CXCL16, in human aortic smooth mus...
deficient animals had increased inflammation and accelerated atherosclerosis. While
CXCL16 levels were found to increase i...
and cardiovascular disease. A major goal in treatment of any chronic disease is
identifying and attempting to control expo...
II. MATERIALS AND METHODS
A. Patient Population
The study population was a convenience sample consisting of patients prese...
chemotherapy, chronic steroid use, patients with autoimmune disorders such as SLE,
rheumatoid arthritis, scleroderma, or o...
indicate high risk for adverse outcomes, severely symptomatic angina patients who are
receiving medical treatment, patient...
mouth periodontal examinations were performed evaluating all teeth present, excluding
third molars. A University of North ...
Calculating mean values can negate localized deep PD if shallow PD are also present,
and a patient with severe disease cou...
The basic steps for the immunoassays utilized in the research study are described
in the following text. Serum samples are...
periodontal disease parameters, CAD, and serum levels of inflammatory mediators.
Data was arranged within the master sprea...
Spearman rank correlation, a non-parametric univariate analysis, was performed
to analyze the association between levels o...
III. RESULTS
A. Patient Recruitment and Demographics
Complete data sets were obtained and analyzed for 51 patients, althou...
although the range was 4.90% to 14.70% demonstrating a great variability of glycemic
control within the population.
C. Cor...
According to the American Academy of Periodontology (AAP), periodontal
disease is classified according to severity of clin...
TABLE 1
SUMMARY STATISTICS
Total patients 51
Average age (years) 55.43 (SD=9.617, range 30-78)
Race
Caucasian, non-Hispani...
TABLE 2
CORONARY ARTERY DISEASE STATUS
Coronary artery disease (CAD) categories % patient population
No CAD 33.3% (n=17)
N...
TABLE 3
PERIODONTAL DISEASE PARAMETERS
Periodontal parameter Average %
per patient
Standard
deviation
Standard error
of me...
E. Serum Levels of Inflammatory Mediators
Serum levels of inflammatory mediators exhibited a large range of values among
t...
of serum IL-18 levels revealed a significant association with statin use (p=0.036), CAL
≥3 mm (p=0.045), and CAL ≥5 mm (p=...
G. Periodontitis and Coronary Artery Disease
Univariate Analyses
Analysis of individual periodontal disease parameters in ...
TABLE 4
SERUM LEVELS OF INFLAMMATORY MEDIATORS
Inflammatory mediator Average
per
subject
Standard
deviation
Standard
error...
TABLE 5
NON-PARAMETRIC UNIVARIATE ANALYSIS OF SERUM LEVELS OF IL-18
AND PERIODONTAL PARAMETERS
(Spearman Rank Correlation)...
TABLE 6
NON-PARAMETRIC UNIVARIATE ANALYSIS OF SERUM LEVELS OF CXCL 16
AND PERIODONTAL PARAMETERS
(Spearman Rank Correlatio...
TABLE 7
NON-PARAMETRIC UNIVARIATE ANALYSIS OF CORONARY ARTERY
DISEASE AND PERIODONTAL PARAMETERS
(Spearman Rank Correlatio...
TABLE 8
MULTIPLE REGRESSION ANALYSIS OF SERUM LEVELS OF IL-18
R2
= 42.45%
Variable Coefficient Standard
error
95% confiden...
TABLE 9
MULTIPLE REGRESSION ANALYSIS OF SERUM LEVELS OF CXCL 16
R2
= 65.98%
Variable Coefficient Standard
error
95% confid...
TABLE 10
MULTIPLE REGRESSION ANALYSIS OF CORONARY ARTERY DISEASE
R2
= 54.03%
Variable Coefficient Standard
error
95% confi...
IV. DISCUSSION AND SUMMARY
Periodontal disease, like coronary artery disease, is a result of the chronic
inflammatory proc...
were prevalent among our patient population. In contrast, multiple regression analysis
identified a statistically signific...
measurement. Additionally, PD and CAL often correlate with each other. With the
exception of psuedopocketing and recession...
and radiographic alveolar bone loss. When evaluating patients in an epidemiologic
research study however, examination and ...
It is interesting to note that complete edentulism has been significantly
associated with coronary artery disease in multi...
periodontal disease if he or she had both CAL and deep PD. Additionally, composite
measures could be developed, in a simil...
atheromas and correlated with atherosclerotic plaque ulcerations as well as clinical
symptoms (Gerdes 2002, Mallat 2001). ...
adverse cardiovascular event such as a myocardial infarction. However, in patients who
are at risk for or are affected wit...
LITERATURE CITED
American Academy of Periodontology Academy Report. Informational Paper: The
pathogenesis of periodontal d...
Daly CG, Mitchell DH, Highfield JE, Grossberg DE, Stewart D. Bacteremia due to
periodontal probing: a clinical and microbi...
Gotsman I, Lotan C, Soskolne WA, Rassovsky S, Pugatsch T, Lapidus L, Novikov Y,
Masrawa S, Stabholz A. Periodontal destruc...
Lester S, Bain J, Johnson R, Serio F. Gingival concentrations of interleukin-23 and -17
at healthy sites and at sites of c...
Mosaad Y, Metwally S, Auf F, Abdel-Samee E, el-Deek B, Limon N, el-Chennawi F.
Proinflammatory cytokines (IL-12 and IL-18)...
Ridker P, Rifai N, Pfeffer M, Sacks F, Lepage S, Braunwald E. Elevation of tumor
necrosis factor-α and increased risk of r...
Taylor BA, Tofler GH, Carey HM, Morel-Kopp MC, Philcox S, Carter TR, Elliott MJ,
Kull AD, Ward C, Schenck K. Full-mouth to...
57
VITA
Rachel Amanda Schallhorn was born on October 28, 1980 to the Reverend Robert
and Frances Schallhorn in Chicago, Il...
Schallhorn Thesis
Upcoming SlideShare
Loading in...5
×

Schallhorn Thesis

1,006

Published on

The Inflamatory Systemic Connection - Gum Disease

Published in: Health & Medicine, Education
0 Comments
0 Likes
Statistics
Notes
  • Be the first to comment

  • Be the first to like this

No Downloads
Views
Total Views
1,006
On Slideshare
0
From Embeds
0
Number of Embeds
0
Actions
Shares
0
Downloads
24
Comments
0
Likes
0
Embeds 0
No embeds

No notes for slide

Transcript of "Schallhorn Thesis"

  1. 1. ANALYSIS OF PERIODONTAL DISEASE IN ASSOCIATION WITH CORONARY ARTERY DISEASE AND INFLAMMATORY MEDIATORS IN PATIENTS UNDERGOING CARDIAC CATHETERIZATION A THESIS Presented to the Faculty of The University of Texas Health Science Center at San Antonio Graduate School of Biomedical Sciences In Partial Fulfillment Of the Requirements For the Degree of MASTER OF SCIENCE Rachel A. Schallhorn, D.D.S. San Antonio, Texas May 2009
  2. 2. ANALYSIS OF PERIODONTAL DISEASE IN ASSOCIATION WITH CORONARY ARTERY DISEASE AND INFLAMMATORY MEDIATORS IN PATIENTS UNDERGOING CARDIAC CATHETERIZATION Rachel A. Schallhorn APPROVED: Supervising professor: Brian L. Mealey, D.D.S., M.S. Devang Patel, MBChB, FACC, FSCAI Thomas Oates, D.M.D., PhD David Lasho, D.D.S., M.S. Paul McLornan, B.D.S. Date APPROVED: Interim Dean, Graduate School of Biomedical Sciences: Robert Reddick, MD
  3. 3. ACKNOWLEDGEMENTS I would like to thank Drs. Brian Mealey, Devang Patel, Thomas Oates, and David Lasho for giving me the opportunity to conduct my research under their supervision. Each member of my supervising committee extended invaluable knowledge, advice, and guidance throughout the investigatory process. I would like to extend special thanks to Dr. Bysani Chandrasekar for time and effort spent both in the research laboratory and at research metings. Without Dr. Chandrasekar’s tireless effort, my investigation would not have been possible. I would also like to acknowledge the cardiology fellows and staff at the University Hospital Cardiac Catheterization clinic who helped make the investigation possible. Finally, I would like to thank my husband, Andrew, for his unfaltering support. iii
  4. 4. ANALYSIS OF PERIODONTAL DISEASE IN ASSOCIATION WITH CORONARY ARTERY DISEASE AND INFLAMMATORY MEDIATORS IN PATIENTS UNDERGOING CARDIAC CATHETERIZATION Rachel A. Schallhorn, M.S. The University of Texas Health Science Center at San Antonio Graduate School of Biomedical Sciences Supervising Professor: Brian L. Mealey Inflammation is a key component in initiation and progression of both periodontal and cardiovascular diseases. Atherosclerosis, an inflammatory process resulting in narrowing of the arterial lumen, can lead to development of coronary artery disease (CAD) predisposing affected patients to acute coronary events. In addition to targeting the classic risk factors in treatment and prevention of CAD, investigation of potential risk iv
  5. 5. factors contributing to the inflammatory component of atherogenesis is at the forefront of preventive cardiology. Interleukin-18 (IL-18) is a pro-inflammatory cytokine present in chronically inflamed tissues, which has been positively associated with increased inflammation and probing depths in patients with periodontitis. Additionally, IL-18 has been associated with clinical signs of an unstable, symptomatic atherosclerotic plaque. CXC ligand 16 (CXCL 16) is a chemokine identified in endothelial cells, smooth muscle cells and macrophages. CXCL 16 is induced by IL-18 expression and functions as an adhesion molecule and scavenger receptor. Investigations of the association between periodontitis and CAD have identified both direct and indirect effects of the chronic inflammatory lesion of periodontitis on the cardiovascular system. The primary aim of this research study was to correlate periodontal parameters with serum levels of IL-18 and CXCL 16 to evaluate a potential indirect association between periodontitis and CAD. The study population was a convenience sample of 51 patients presenting for clinically indicated coronary angiography. Clinical information collected prior to catheterization included demographics, body mass index, blood pressure, history of statin use, smoking status, presence of cardiac risk factors such as diabetes and family history, and serum C-reactive protein levels. CAD was classified according to presence and extent as follows: no CAD, non-obstructive CAD (<50 % occlusion), and CAD (>50 % occlusion) affecting 1-, 2-, 3-, or 4-vessels. Venous blood was collected at the time of catheterization and used to determine serum levels of inflammatory mediators IL-18 and CXCL16. Periodontal status was evaluated by a full mouth clinical periodontal exam at 6 sites per tooth. The percent of sites with probing depth (PD) ≥5 mm and ≥7 mm, clinical attachment loss (CAL) ≥3 mm and ≥5 mm, and bleeding on probing (BOP) were v
  6. 6. recorded to determine the extent and severity of periodontitis. Correlations between periodontal parameters, levels of inflammatory mediators, and CAD status were analyzed using the univariate analysis Spearman Rank Correlation and multiple regression. The percent of sites with BOP exhibited a significant positive correlation with serum levels of IL-18 in non-parametric univariate analysis (p=0.0389) indicating a correlation between periodontal inflammation and systemic levels of IL-18. When multiple regression analysis was performed, extent of CAL ≥3 mm (p=0.0452) and CAL ≥5 mm (p=0.0242) exhibited a significant association with IL-18. Statin use also exhibited a significant association with IL-18 (p=0.0361). Multiple regression analysis of CXCL16 identified a statistically significant association with CAL ≥5 mm (p=0.040) and PD ≥7 mm (p=0.047). In addition a statistically significant association between CXCL16 levels and smoking was also identified (p=0.0054). Multiple regression analysis of CAD also identified a significant association with CAL ≥3 mm (p=0.0471). Periodontal inflammatory mediators are similar to those involved in development of the atherosclerotic lesion. Analysis of our patient population suggests a significant association between periodontitis and serum levels of IL-18, CXCL16 and the presence of CAD. Elevated levels of IL-18 and CXCL16 associated with the inflammatory lesion of periodontitis may indirectly contribute to development of atherosclerosis and thus place patients at increased risk for CAD. vi
  7. 7. TABLE OF CONTENTS Page Title ……………………………………………………………………………. i Approval ………………………………………………………………………. ii Acknowledgements ……………………………………………………………. iii Abstract ……………………………………………………………………….. iv Table of Contents ………………………………………………………........... v List of Tables ………………………………………………………………….. vi 1. INTRODUCTION AND LITERATURE REVIEW ………………….. 1 A. Periodontal Disease as an Inflammatory Disease ………… 1 B. Coronary Artery Disease as an Inflammatory Disease …….. 6 C. Periodontal Disease and Coronary Artery Disease Interrelationships ………………………………………. 8 D. Interleukin-18, CXCL16 and Inflammatory Diseases …….. 12 E. Specific Research Objectives ……………………………… 16 2. MATERIALS AND METHODS ………………………………………. 18 A. Patient Population ………………………………………… 18 B. Cardiac Catheterization and Clinical Data Collection ……… 19 C. Periodontal Examination …………………………............… 20 D. Serum Levels of Inflammatory Mediators …………............. 22 E. Data Entry and Statistical Analysis …………………............ 23 3. RESULTS ……………………………………………………………….. 26 4. DISCUSSION AND SUMMARY ………………………………............. 42 5. LITERATURE CITED ………………………………………………….. 50 vii
  8. 8. viii LIST OF TABLES Page Table 1 Summary Statistics ……………………………………................. 29 Table 2 Coronary Artery Disease Status ………………………................. 30 Table 3 Periodontal Disease Parameters …………………………………. 31 Table 4 Serum Levels of Inflammatory Mediators ………………………. 35 Table 5 Non-Parametric Univariate Analysis of Serum Levels of IL-18 and Periodontal Parameters (Spearman Rank Correlation) ……… 36 Table 6 Non-Parametric Univariate Analysis of Serum Levels of CXCL16 and Periodontal Parameters (Spearman Rank Correlation) ……… 37 Table 7 Non-Parametric Univariate Analysis of CAD and Periodontal Parameters (Spearman Rank Correlation) ……………………….. 38 Table 8 Multiple Regression Analysis of Serum IL-18 …………………... 39 Table 9 Multiple Regression Analysis of Serum CXCL16 ………………. 40 Table 10 Multiple Regression Analysis of CAD …………………………… 41
  9. 9. I. INTRODUCTION AND LITERATURE REVIEW A. Periodontitis as an Inflammatory Disease Periodontal disease is characterized as a chronic, low-grade infection involving the supporting structures of the teeth. While bacteria are a necessary etiologic agent they are not sufficient to establish disease. Evidence clearly demonstrates the role of inflammation in periodontal disease initiation and progression. The host response to bacteria within a biofilm ranges from the initial, neutrophil-dominated lesion of gingivitis to the established, plasma cell-dominated lesion of periodontitis (Page 1976). The long- standing lesion of periodontitis represents a chronic bacterial infection not effectively neutralized by host immune defenses, thus perpetuating an inflammatory state. Although active infection is generally localized to the periodontal pocket, bacteria and bacterial products, such as lipopolysaccharide (LPS), as well as locally produced inflammatory mediators may gain access to the systemic circulation through the ulcerated pocket epithelium (Loos 2000, Loos 2005). Numerous studies evaluating local and systemic levels of inflammatory mediators have found a positive correlation with periodontal disease. Among the studied inflammatory mediators, those identified as having a positive association with periodontitis include C-reactive protein (CRP), interleukin-1 (IL-1), interleukin-6 (IL-6), interleukin-8 (IL-8), tumor necrosis factor-alpha (TNF-α), and prostaglandin E2 (PGE2) among many others. Analysis of the third National Health and Nutrition Examination Survey (NHANES III) revealed a positive correlation between extensive periodontal disease and serum CRP levels (Slade 2000). In a cross-sectional study evaluating 1
  10. 10. periodontal status and subgingival periodontal pathogens, Noack and colleagues identified significantly higher mean CRP levels in subjects with periodontal disease versus periodontally healthy subjects (Noack 2001). Additionally, the presence of one or more periodontal pathogens had a direct and significant correlation with mean CRP levels. Analysis of periodontal status and CRP levels in a cohort of men enrolled in a study of cardiovascular disease showed a significant association between advanced periodontitis and elevated CRP levels, adjusting for cardiovascular risk factors, at two time-points over a 20-year period (Linden 2008). An intervention trial evaluating CRP and IL-6 in 94 patients with generalized severe periodontitis, demonstrated significant decreases in serum levels of both inflammatory mediators over the 6 month observation period (D’Aiuto 2004). In addition, initial assessment of the participants revealed a significant association between more extensive periodontitis (greater than the median number of periodontal pockets with PD ≥5 mm) and CRP levels >3 mg/L. A recent systematic review and meta-analysis of CRP in relation to periodontitis concluded “there is strong evidence from cross-sectional studies that plasma CRP in periodontitis is elevated compared with controls” and “modest evidence on the effect of periodontal therapy in lowering the levels of CRP” (Paraskevas 2008). In addition to acute phase reactants, signaling molecules involved in orchestration of the immune response, such as cytokines and chemokines, have also been implicated in the pathogenesis of periodontal disease. According to the American Academy of Periodontology Academy Report, the pathogenic mechanisms of periodontitis are not fully understood, however inflammatory mediators consistently associated with periodontitis include the following: IL-1 and TNFα, pro-inflammatory multifunctional 2
  11. 11. cytokines; IL-6, a pro-inflammatory cytokine involved in osteoclast formation and plasma cell proliferation; IL-8, a pro-inflammatory chemokine produced by monocytes in response to lipopolysaccharide and pro-inflammatory cytokines; and prostaglandin E2 which induces bone resorption and matrix metalloproteinase secretion (American Academy of Periodontology 1999). A study evaluating untreated periodontitis patients versus healthy, age-matched controls identified a positive association between radiographic bone loss and serum levels of CRP, IL-6, and neutrophil count (Loos 2000). In a case series of patients classified at high risk for atherosclerosis, non-surgical periodontal therapy combined with local delivery of minocycline-HCl significantly reduced circulating levels of both CRP and TNFα (Iwamoto 2003). Data from studies of the local environment of a periodontal lesion parallel findings from studies evaluating levels of inflammatory mediators in the systemic circulation. Comparison of gingival crevicular fluid (GCF) samples collected from healthy gingival sulci versus periodontal pockets further demonstrates the heightened level of inflammation associated with active periodontal disease. Prostaglandin E2, a multifunctional proinflammatory mediator, has been associated with progressive attachment loss in both human and animal studies (Offenbacher 1993). In a study comparing GCF IL-1β levels among patients with varying severities of periodontal disease, increased levels of the pro-inflammatory cytokine were detected in both site- based and patient-based analyses. Sites with increased probing depth and attachment loss, as well as patients with severe versus mild-moderate disease, exhibited higher levels of GCF IL-1β (Engbretson 2002). A recent study evaluated GCF levels of IL-1β, IL-11, and IL-12 in chronic periodontitis, gingivitis, and periodontal health. Results indicated 3
  12. 12. chronic periodontitis patients had significantly higher levels of IL-1β and IL-12, while IL-11 exhibited an inverse correlation with periodontal disease (Yucel 2008). An intervention trial evaluating the effect of surgical anti-infective therapy for peri- implantitis on local levels of TNFα identified a significant decrease in TNFα in the crevicular fluid (Duarte 2009). Moreover decreased TNFα levels were positively and significantly correlated with decreased probing depth and bleeding on probing. In addition to fluid collected from the periodontal pocket, tissue and cells collected from diseased sites exhibit similar findings. In a study of twelve patients with periodontal disease, tissue biopsies harvested from both active and stable sites showed elevated levels of IL-1β in sites exhibiting attachment loss over the study period (Stashenko 1991). Local inflammatory infiltrate and mRNA expression of pro- inflammatory cytokines has been shown to differ between diseased and healthy patients. A research study comparing gingival biopsies between healthy patients and those with either chronic or generalized aggressive periodontal disease, found the diseased patients had significantly increased neutrophil infiltration and mRNA expression of IL-1β and TNF-α (Liu 2001). In vitro studies have demonstrated cells harvested from inflamed sites maintain their phenotypic characteristics and have increased expression of pro- inflammatory cytokines compared with cells from non-inflammed tissue. Gingival fibroblasts harvested from sites affected by periodontitis have been shown to produce more IL-6 constituitively and following treatment with bacterial LPS and IL-1α (Kent 1999). Increased expression of pro-inflammatory cytokines by human gingival fibroblasts harvested from chronic periodontitis patients has also been shown to positively correlate with their in situ expression within the tissue from which the cells 4
  13. 13. were harvested. Fibroblasts from diseased tissue were shown to have higher constituitive expression of IL-6 and IL-8 compared to those from healthy sites; additionally, authors suggested the cells were phenotypically inclined to secrete increased levels of the inflammatory mediators (Dongari-Bagtzoglou 1998). Emerging evidence points to a role for more recently discovered cytokines in the pathogenesis of periodontitis. Interleukin-17 (IL-17) is a novel, multi-functional cytokine which is thought to be involved in both the innate and adaptive immune responses. Available evidence promotes the role of IL-17 in autoimmunity and bone loss (Kramer 2007). Analysis of gingival biopsies from sites with minimal (0-2 mm), moderate (3-4 mm), and severe (≥5 mm) CAL revealed a significant positive correlation between CAL and concentrations of IL-23, IL-17, IL-6, IL-1β, and TNFα (Lester 2007). In addition to IL-17, interleukin-18 (IL-18) has been implicated in maintenance of local chronic inflammation (Delaleu 2004). An investigation evaluating cytokine levels in human gingival biopsies found a significant positive correlation between IL-6 and IL-18 concentrations and probing depth (Johnson 2005). In addition to identifying an association between inflammatory mediators and periodontal disease, a causal effect has been established in animal models. An investigation in non-human primates, utilizing local injection of IL-1 soluble receptors combined with experimental periodontitis, identified increased progression of inflammation toward alveolar bone compared to non-injected control animals (Graves 1998). Conversely, inhibition of IL-1 and TNF activity utilizing soluble receptor blockers has been shown to inhibit loss of connective tissue attachment in a similar animal model (Delima 2001). Gene therapy has also been utilized in animal models to 5
  14. 14. reduce levels of inflammatory mediators and limit alveolar bone loss (Cirelli 2008). Establishment of a cause-and-effect relationship between inflammatory cytokines and periodontitis provides a potential target for innovative periodontal therapy. B. Coronary Artery Disease as an Inflammatory Disease Coronary artery disease (CAD) is a leading cause of morbidity and mortality in the United States. A major component in development of CAD is atherosclerosis, an inflammatory process that can result in narrowing of the affected arterial lumen predisposing affected patients to acute coronary events. The progression of atherosclerosis, as described by Ross (1999), consists of 4 distinct stages. Initially endothelial dysfunction within the affected artery occurs. The result is increased endothelial permeability to lipoproteins and other molecules in the plasma as well as up- regulation of leukocyte and endothelial adhesion molecules. Fatty streak formation follows endothelial dysfunction; it is characterized by accumulation of foam cells (lipid- filled macrophages) and T lymphocytes within the vessel wall, vascular smooth muscle cell proliferation, and platelet adherence and aggregation. Since resolution of the lesion cannot be achieved, the inflammatory process continues ultimately forming a fibrous cap covering the lesion. At this point the atheroma or plaque is considered an advanced, complicated lesion. In the final stage, the fibrous cap becomes ruptured or ulcerated. The lesion is considered an unstable fibrous plaque and the affected artery is at high risk for thrombosis (Ross 1999). Inflammatory mediators orchestrate the complex sequence of events leading to development of an advanced atherosclerotic lesion (Zernecke 2005). Of the mediators involved, pro-inflammatory cytokines and chemokines play a prominent role. 6
  15. 15. In addition to targeting the classic risk factors in the treatment and prevention of cardiovascular disease (CVD), investigation of potential risk factors contributing to the inflammatory component of atherogenesis is at the forefront of preventive medical research. Classic risk factors include smoking, serum cholesterol and obesity, while examples of potential risk factors include elevated levels of inflammatory markers such as CRP and pro-inflammatory cytokines (Lowe 2001). The relationship between CRP and cardiovascular disease has been extensively studied. A 2003 American Heart Association and Center for Disease Control scientific statement concluded measurement of high sensitivity-CRP, as an adjunct to assessment of “major” risk factors, may be useful in assessing risk for adverse cardiac events (Pearson 2003). Interleukin-6 and TNFα have also been evaluated in relationship to cardiovascular diseases, albeit to a lesser extent than CRP. A prospective study of 14,916 apparently healthy men found elevated levels of serum IL-6 were associated with occurrence of myocardial infarction over the study period (Ridker 2000a). A cross-sectional study evaluating 147 patients undergoing coronary angiography demonstrated serum levels of IL-6, fibrinogen, and CRP positively correlated with extent of coronary stenosis (Erren 1999). In a nested case-control study evaluating patients who previously had myocardial infarction (MI), patients experiencing a recurrent MI within the 5 year follow-up period (cases) had persistently elevated plasma levels of TNFα compared to controls (Ridker 2000b). Evidence clearly demonstrates systemic inflammation is elevated in patients with coronary artery disease. The degree and extent to which specific inflammatory mediators influence the disease process is not, however, clearly understood. Deciphering the 7
  16. 16. complex chain of events leading to atherosclerosis and identifying potential therapeutic targets remains the focus of ongoing research. C. Periodontal Disease and Cardiovascular Disease Interrelationships While an association between periodontitis and coronary artery disease has been established, the mechanism of this association has not been fully elucidated. Investigations have focused on both the direct and indirect effects of chronic inflammation in the periodontium on the cardiovascular system. The direct systemic effects of periodontitis involve local elements of the periodontal pocket that have gained access to the systemic circulation. Bacteremia and endotoxemia of oral origin can result from various stimuli in the oral cavity and have been positively correlated with periodontitis. A study evaluating systemic levels of endotoxin following mastication, found a significantly increased level and prevalence of endotoxemia in patients with severe periodontitis compared to healthy controls (Geerts 2002). An investigation of periodontal probing identified oral bacteria in the peripheral venous blood in 40% of periodontitis patients versus 10% of gingivitis patients (Daly 2001). Bacteremia was significantly associated with bleeding on probing and probing depth. A mechanism by which bacteria may affect the vasculature is through systemic release of endotoxin. Available evidence in cardiovascular literature also implicates endotoxin in promoting chronic inflammation and predisposing patients to atherosclerosis. Endotoxin is thought to contribute to atherosclerosis through induction of proinflammatory cytokines, chemokines, acute phase reactants, and adhesion molecules (Stoll 2004). Results from a large-scale prospective study evaluating changes in carotid atherosclerosis over a 5-year period demonstrated 40% of new atherosclerotic lesions were attributable to chronic 8
  17. 17. systemic infection (Kiechl 2001). Another notable observation was that the risk of atherosclerosis tended to be higher in patients with chronic infection and a prominent inflammatory response; authors implicate either highly virulent pathogens or an atherogenic host response. In addition to transiently entering the vascular system, bacterial DNA has been isolated from atheroma specimens; however, there is conflicting evidence as to their origin. In an analysis of 50 carotid atheroma specimens, 44% were found to contain 16S rDNA from periodontal pathogens (Haraszthy 2000). A more recent study analyzed subgingival plaque samples and atheroma specimens in 33 patients undergoing carotid endarterectomy. While bacterial DNA was isolated in 31 out of 33 atheroma specimens, no DNA from periodontal pathogens was found (Aimetti 2007). A similar investigation identified the same periodontal pathogens in subgingival and coronary artery atherosclerotic plaque samples in 10 out of 20 patients. Furthermore patients with bacteria in their atherosclerotic lesions had a significantly higher mean bleeding score (Zaremba 2007). Results from the aforementioned studies confirm that bacteria, bacterial products, and inflammatory mediators involved in the pathogenesis of periodontitis do not remain at the site of infection. While the effect these organisms and mediators have upon other systems in the body is not known, it does represent a potential link between oral and systemic disease. The indirect association between periodontitis and systemic disease may be mediated through upregulation of inflammatory mediators in the systemic circulation due to localized infection. The phenomenon of increased systemic inflammation resulting 9
  18. 18. from a local infection is well supported in periodontal literature, as cited in section A of the literature review. In order to explore the systemic effect of reducing or eliminating infection and inflammation in the oral cavity, it is necessary to examine results from intervention trials. Published data from interventional trials demonstrates a positive systemic effect can be achieved with periodontal treatment. Full mouth extraction, performed in adults diagnosed with severe periodontitis and a terminal dentition, has been shown to precipitate significant decreases in systemic levels of CRP, plasminogen activator inhibitor, and white blood cell counts (Taylor 2006). A pilot intervention trial evaluated the effects of traditional versus intensive initial periodontal therapy in a group of 40, otherwise healthy, severe chronic periodontitis patients (D’Aiuto 2006). The intensively treated group received local antimicrobial therapy in addition to scaling and root planing. Intensive initial therapy resulted in significant decreases in IL-6, CRP, total cholesterol, and systolic blood pressure. A recent focus of intervention trials has been the association between periodontal disease and endothelial dysfunction. Endothelial dysfunction is a component of coronary artery disease and is characterized by a decreased vascular response to increased shear stress on the vascular wall in combination with normal dilation in response to sublingual nitroglycerine. An investigation of endothelial function in 30 severe periodontitis patients and 31 periodontally healthy control patients identified significantly lower baseline flow-mediated vasodilation in patients with periodontitis (Seinost 2005). Non- surgical periodontal therapy resulted in a significant improvement in endothelial function and a concomitant decrease in CRP levels. The results of standard versus intensive 10
  19. 19. periodontal therapy on endothelial dysfunction were analyzed in a randomized controlled clinical trial (Tonetti 2007). One-hundred and twenty patients with generalized severe periodontitis were assigned to receive either supragingival scaling (control) or scaling and root planing with local minocycline delivery and extraction of hopeless teeth (intensive). Results indicated scaling and root planing increased levels of CRP and IL-6 as well as endothelial activation markers E-selectin and vonWillebrand factor. In addition, reduced flow-mediated dilation indicating endothelial dysfunction was seen within the first 24 hours after scaling and root planning. Re-evaluation at 2 and 6 months, however, showed flow-mediated dilation was significantly higher in the test group, suggesting a long-term benefit from intensive periodontal therapy. The above cited intervention trials demonstrate a direct relationship between periodontal inflammation and endothelial dysfunction, thus lending strength to the association between periodontal and coronary artery diseases. Review of the evidence clearly demonstrates inflammation is a key component in initiation and progression of both periodontal and cardiovascular disease. The pathologic process in both cases results from tipping the delicate balance of inflammation toward a destructive rather than protective pathway. Although much has been discovered through clinical and laboratory investigations, the pathogenesis and interrelationship of periodontal disease and atherosclerosis are not fully understood. Evaluating periodontal and cardiovascular diseases is difficult due to their chronic and multifactorial nature. Contributing factors involved in the pathogenesis of both diseases, such as smoking and diabetes, also obscure the relationship. A review of the available evidence reveals significant heterogeneity among research studies both in study design and definitions of 11
  20. 20. disease (Beck 2005); hence a strong relationship between periodontal and cardiovascular disease cannot be readily established. Despite the relative lack of prospective longitudinal studies and intervention trials, available evidence supports a moderate association between periodontal disease and atherosclerosis-induced diseases such as CAD, stroke, and peripheral vascular disease (Scannapieco 2003). An evaluation of clinical periodontal parameters and radiographic alveolar bone loss (ABL) in 110 patients diagnosed with coronary heart disease versus 140 healthy controls identified a statistically significant association between ABL >4 mm and coronary heart disease, with an odds ratio of 6.6 (Geismar 2006). Another case-control study evaluating periodontal status in 90 males, 45 with and 45 without CAD, found significantly deeper mean probing depths (PD) and greater mean clinical attachment loss in patients with angiographically confirmed CAD (Nonnenmacher 2007). While the majority of research studies evaluating this relationship are cross-sectional in nature and thus cannot establish causality, they do contribute to our current body of knowledge and provide a basis for future research. D. Interleukin-18, CXCL16 and inflammatory diseases Advancements in technology have led to an exponential increase in our knowledge of the immune system and pathogenesis of disease. These innovations have led to the discovery of previously unidentified inflammatory mediators whose roles in inflammatory processes are currently being investigated. Among these more recently identified inflammatory mediators are those of primary interest in this investigation: interleukin-18 (IL-18) and CXCL16. 12
  21. 21. Interleukin-18 (IL-18) is a pro-inflammatory cytokine and is a member of the interleukin-1 superfamily. It is expressed in sites of chronic inflammation. IL-18 has been shown to induce IFNγ, both alone and synergistically with IL-12, hence promoting the Th1 immune response (Johnson 2005). In order for inflammation to resolve, a shift from a Th1 dominated response to a Th2 response must generally occur. Researchers have hypothesized a sustained Th1 response leads to development of chronic inflammation (Gemmell 2004). Upregulation of IL-18 has been identified in association with several chronic diseases including inflammatory bowel disease (Sanches-Munoz 2008), Sjogren’s syndrome (Manoussakis 2007), systemic lupus erythematosus, rheumatoid arthritis (Mosaad 2003), and atherosclerosis. Immunohistochemistry of human atheroma tissue identified IL-18 and its functional receptor localized within lesional macrophages; neither IL-18 nor its receptor were found in non-diseased human arterial tissue (Gerdes 2002). When human macrophages and smooth muscle cells were treated with recombinant human IL-18, they induced IFNγ expression. Taken together, these observations suggest IL-18 is involved in development of atherosclerotic lesions. While IL-18 is known to be involved in the early stages of inflammation, it also appears to modulate the cytokine cascade at later points (Gracie 2002). Increased levels of IL-18 are present during acute coronary syndromes. In order to evaluate the association between IL-18 and later stages of atherosclerosis, IL- 18 expression was analyzed in 40 human carotid atherosclerotic plaques and correlated to intraplaque ulceration and clinical symptoms (Mallat 2001). Results revealed IL-18 expression was significantly higher when clinical signs of an unstable, symptomatic plaque were evident and when plaque ulcerations were present. 13
  22. 22. The association between IL-18 and periodontal disease has also been investigated, albeit to a lesser extent than in the cardiovascular literature. While laboratory studies have linked IL-18 expression to periodontal pathogens, clinical studies have correlated IL-18 levels with the presence and severity of periodontal disease. An in vitro study, evaluating cytokine expression in human monocytes, demonstrated exposure to Porphyromonas gingivalis resulted in IL-18 expression (Hamedi 2008). Clinical investigations have evaluated IL-18 levels in periodontal tissues and GCF. Johnson and Serio (2005) correlated levels of IL-18 in gingival biopsies to parameters of periodontal inflammation and probing depth. Interleukin-18 was significantly higher in tissue harvested from sites with severe disease (PD >6 mm) compared to healthy sites. Assays of GCF in 10 periodontitis and 10 gingivitis patients demonstrated IL-18 levels were significantly higher in patients with periodontitis (Orozco 2006). A more recently published study reached a similar conclusion. Pooled subgingival plaque and GCF samples from deep (PD ≥5 mm) and shallow (PD ≤3 mm) sites of 18 periodontitis patients were analyzed; investigators found significantly higher IL-18 levels compared to gingivitis patients (Figueredo 2008). No association was identified between IL-18 and the presence of red complex bacteria. Available evidence clearly demonstrates an association between periodontal disease and local expression of IL-18. The effect periodontal inflammation has on systemic IL-18 levels, and the sequelae of the relationship, is yet to be determined. CXCL16 is a pro-inflammatory chemokine. It has been shown to promote cell- cell adhesion, act as a scavenger receptor promoting foam cell formation, and induce smooth muscle cell proliferation. CXCL16 exerts its effects through transmembrane 14
  23. 23. receptor CXCR6. Lipopolysaccharide has been shown to upregulate CXCR6, the receptor for CXCL16, in human aortic smooth muscle cells resulting in delayed but persistent increases in level of expression (Patel 2006). Results from this investigation promote the idea that endotoxemia or chronic low levels of endotoxin may contribute to atherogenesis. CXCL16 and CXCR6 have been found to be expressed in both human and murine atherosclerotic lesions. An investigation evaluating the effect of IFNγ on human monocytes found IFNγ can induce upregulation of CXCL16 which then results in increased ox-LDL uptake by the monocytes (Wuttge 2004). Monocytic uptake of ox- LDL results in foam cell formation, a component of early atherosclerosis. Less evidence is available linking CXCL16 with periodontal disease. Hosokawa and colleagues (2001) investigated CXCL16 and CXCR6 mRNA expression within diseased and healthy periodontal tissues. Although CXCL16 mRNA was detected in healthy periodontal tissue, it was more heavily expressed within diseased tissue. Further analysis of the diseased tissue demonstrated CXCL16 was strongly expressed by fibroblasts and CXCR6-positive cells were generally distributed near the sulcular epithelium. Moreover, harvested human gingival fibroblasts were shown to significantly upregulate CXCL16 mRNA expression when treated with pro-inflammatory cytokines IL-1β, TNF-α, and IFN-γ (Hosokawa 2007). Considering the available evidence, CXCL16 is likely involved in the pathogenesis of both atherosclerosis and periodontitis. It is hypothesized that circulating levels of CXCL16 may serve as a marker to predict future development of coronary heart disease (CHD) (Sheikine 2008). Conflicting evidence exists, however, suggesting CXCL16 may have an atheroprotective effect. In a laboratory study using a murine model, investigators found CXCL16- 15
  24. 24. deficient animals had increased inflammation and accelerated atherosclerosis. While CXCL16 levels were found to increase in the aortic arch under pro-atherogenic conditions, authors suggest scavenger receptor activity of CXCL16 may in fact be atheroprotective (Aslanian 2006). In human subjects, significantly lower levels of serum CXCL16 were identified in stable angina patients versus healthy controls; again suggesting a relationship between atherosclerosis and lack of CXCL16 and its protective activity (Sheikine 2006). CXCL16 may work synergistically with IL-18 in the pathogenesis of atherosclerosis. Results from a laboratory study evaluating the effects of IL-18 in rat aortic smooth muscle cells, demonstrated IL-18 induces smooth muscle cell proliferation in a CXCL16-dependent manner (Chandrasekar 2005). The aforementioned study implicates IL-18-CXCL16 cross-talk in atherogenesis. Laboratory studies evaluating atherogenesis in immunodeficient mice have found that the proatherogenic role of IL-18 may partially depend on IFNγ-mediated upregulation of CXCL16 (Tenger 2005). It is evident both IL-18 and CXCL16 have a role in coronary artery disease and possibly periodontal disease as well. The extent to which the inflammatory mediators influence the disease process, however, is unknown. E. Specific Research Objectives The association between periodontal disease and cardiovascular disease has long been recognized, however the mechanisms behind this association remain obscure. Numerous studies have been published over the past few decades including case-control, cross-sectional, and longitudinal observational studies. The majority of studies have identified a low to moderate, yet significant, level of association between periodontitis 16
  25. 25. and cardiovascular disease. A major goal in treatment of any chronic disease is identifying and attempting to control exposure to factors placing patients at risk for development of the disease. Increased levels of circulating pro-inflammatory mediators have been identified as potential risk factors for development of coronary artery disease and associated adverse cardiac events. Further elucidation of the indirect relationship between periodontal and cardiovascular diseases may lead to improved medical care for at-risk patients. The purpose of this research study was to examine the relationship between periodontal disease and coronary artery disease in association with pro-inflammatory mediators. Therefore, the specific aims were as follows: 1. To investigate the association between periodontal disease and serum levels of inflammatory mediators IL-18 and CXCL16. 2. To investigate the association between periodontal disease and coronary artery disease. 3. To investigate the association between inflammatory mediators IL-18, CXCL16, and coronary artery disease. The overall goal of the study was to investigate specific systemic inflammatory consequences of periodontal disease and their potential indirect role in contributing to the development of coronary artery disease and predisposing affected patients to adverse cardiac events. A positive correlation between periodontal disease and the inflammatory markers IL-18, and CXCL16 could represent a common pathogenic mechanism between periodontal disease and coronary heart disease and might infer increased risk for development of adverse cardiac events in patients with periodontitis. 17
  26. 26. II. MATERIALS AND METHODS A. Patient Population The study population was a convenience sample consisting of patients presenting for clinically indicated coronary angiography at the University Hospital cardiology clinic of the University of Texas Health Sciences Center San Antonio (UTHSCSA). An ongoing research study was in progress at the facility with a specific aim to examine the relationship between IL-18, CXCL 16 and CAD; the patients receiving a periodontal examination are a subset of this larger patient population. The study protocol was approved by the Institutional Review Board of UTHSCSA. Each patient read and signed a detailed consent form prior to participation in the study. Patients were recruited during their pre-catheterization appointment, which is generally scheduled approximately one week prior to the cardiac catheterization. A cardiology fellow performed pre-catheterization examinations and identified patients meeting the inclusion criteria for participation in the research study. Patients consenting to participate received a periodontal examination during their pre-catheterization appointment. At the time of cardiac catheterization the presence, severity, and extent of CAD was determined and recorded. A blood sample was obtained from the patient at the time of catheterization for analysis of inflammatory mediators. Exclusion criteria for participation in the study included the following: patients requiring endocarditis prophylaxis, patients unable or unwilling to undergo diagnostic angiography, patients unable or unwilling to participate in the research study, patients with active systemic infections evident by fevers and leukocytosis, patients on antibiotics recovering from systemic infection, immunosuppressed patients due to HIV/AIDS, 18
  27. 27. chemotherapy, chronic steroid use, patients with autoimmune disorders such as SLE, rheumatoid arthritis, scleroderma, or other significant connective tissue diseases, patients admitted for chest pain or acute coronary syndromes associated with the use of cocaine. Patients with active infection, systemic conditions outlined above, or use of certain medications including antibiotics or steroids were excluded due to the effect these variables can have on systemic cytokine levels. B. Cardiac Catheterization and Clinical Data Collection Clinical data collection was performed at the time of the pre-catheterization examination. Clinical data collected include patient characteristics and results of pertinent laboratory tests and are listed as follows: age, gender, race, smoking status, patient reported family history of cardiovascular disease, body mass index (BMI) as calculated from height and weight, history of statin medication use, blood pressure, triglycerides, total cholesterol, low-density lipoprotein (LDL), high-density lipoprotein (HDL), serum CRP, and hemoglobin A1c values for diabetic patients. Smoking status, as determined by patient report, was classified into four categories as follows: 1= never smoke, 2= quit more than one year prior, 3= quit four weeks to one year prior, and 4= active smoker. Information regarding patient characteristics was recorded at the pre- catheterization appointment. Laboratory values were collected from recent tests, which had been recorded in the patients’ electronic medical records. Cardiac catheterization was performed at University Hospital in the cardiology unit based upon clinical indications. According to the American College of Cardiology and American Heart Association Practice Guidelines, clinical indications for coronary angiography include, but are not limited to, the following: non-invasive test results 19
  28. 28. indicate high risk for adverse outcomes, severely symptomatic angina patients who are receiving medical treatment, patients who have been resuscitated from sudden cardiac death, and patients who have sustained monomorphic ventricular tachycardia or nonsustained polymorphic ventricular tachycardia (Scanlon 1999). The majority of patients enrolled in the present study were referred for coronary angiography based upon results from a recent, non-invasive stress test. A minority of the patients enrolled in the study were referred for coronary angiography as a preoperative evaluation prior to noncardiac surgery. Results from the coronary angiography were obtained from the patients’ electronic health records as it was not feasible for the investigator to be present during each of the catheterization procedures. The coronary angiography procedure evaluated the presence and extent of coronary artery stenosis, left ventricular end-diastolic pressure, left ventricular ejection fraction, and the treatment decision based upon catheterization results. If occlusion of a vessel was identified, it was recorded by the percent of stenosis. Stenosis less than 50% was diagnosed as non-obstructive CAD and ≥50% stenosis was classified as CAD. When CAD was present, the number of vessels affected were recorded, which represented extent of the disease. C. Periodontal Examination Periodontal examination was performed during the pre-catheterization appointment prior to cardiac catheterization. Patients were assigned an identification number at the time of periodontal examination; the same number was used on clinical data collection forms and for labeling blood samples. All examinations were performed by Dr. Rachel Schallhorn utilizing a portable headlamp to aid in visualization. Full 20
  29. 29. mouth periodontal examinations were performed evaluating all teeth present, excluding third molars. A University of North Carolina (UNC) probe was utilized to evaluate six sites per tooth for probing pocket depth (PD), recession, and bleeding on probing (BOP). Bleeding on probing was recorded using a dichotomous index (present or absent). Clinical attachment level (CAL) was calculated by adding recession and PD. A dichotomous, visual plaque index was recorded at four sites per tooth. Information collected from the periodontal exam was recorded on a periodontal charting form and later entered into an electronic spreadsheet. When evaluating PD, two thresholds were set representing moderate disease with PD ≥5 mm and severe disease with PD ≥7 mm. Probing depth is a standard measure of periodontal disease. Deep PD is associated with increased numbers of periodontal pathogens within the subgingival plaque (Socransky 1998) and progressive loss of attachment (Claffey 1990). The inflammation of the supporting periodontal tissues generally leads to loss of connective tissue attachment and alveolar bone. A standard measure for attachment loss and alveolar bone destruction is clinical attachment level (CAL). Loss of clinical attachment reflects a history of destructive periodontitis and does not necessarily indicate active inflammatory disease. In order to measure active inflammation, BOP was evaluated. Bleeding on probing has consistently been associated with active inflammation and disease progression, both clinically (Schaetzle 2003) and histologically (Greenstein 1984). For each patient, periodontal disease parameters were analyzed as the percent of sites involved. Analyzing patients by frequency distributions, rather than mean values, takes into account the site specific nature of periodontal disease. Epidemiologic studies have shown severe periodontitis more frequently affects posterior teeth (Albandar 1999). 21
  30. 30. Calculating mean values can negate localized deep PD if shallow PD are also present, and a patient with severe disease could be potentially misrepresented. D. Serum Levels of Inflammatory Mediators Serum levels of inflammatory mediators were determined using blood samples obtained from patients during the cardiac catheterization. The catheterization procedure necessitates placement of a sheath into the femoral artery; after successful completion of the procedure, 10 mililiters of blood were collected from the sheath access. Once blood samples were collected they were stored at -80°C in the research laboratory of Dr. Bysani Chandrasekar at UTHSCSA. Serum was obtained by centrifugation of whole blood and analyzed in two separate batches. Sera from the first 15 patients were assayed after one year of patient recruitment; samples from the remaining participants were assayed after patient recruitment was concluded (after approximately 2 years of patient recruitement). All sample analysis was performed by Dr. Bysani Chandrasekar. Quantification of serum levels of IL-18 and CXCL 16 was performed utilizing enzyme linked immunosorbent assay (ELISA). Serum levels of IL-18 were analyzed using a quantitative test kit for human IL-18 manufactured by MBI International Corporation. Serum levels of CXCL16 were analyzed using a quantitative test kit for human CXCL16 known as Quantikine® manufactured by R&D Systems, Incorporated. Both immunoassays employ a sandwich technique utilizing two monoclonal antibodies, which bind to different epitopes on the inflammatory mediator being evaluated. The procedures for quantification of IL-18 and CXCL16 are nearly identical with the exception of small variations in incubations times (30-60 minutes). 22
  31. 31. The basic steps for the immunoassays utilized in the research study are described in the following text. Serum samples are first diluted; appropriate dilution factors are determined by the investigator. Samples and standards are placed into wells coated with anti-human IL-18 antibody and incubated at room temperature (20-25°C) for 60 minutes. Well contents are aspirated and the wells are washed four times with a buffer solution. Then, a peroxidase-conjugated anti-human IL-18 antibody is placed into the wells and incubated at room temperature for 60 minutes. Well contents are aspirated and the wells are again washed. A peroxidase substrate is then placed into the wells and incubated at room temperature for 30 minutes. Following incubation, an acid solution is added to each well in order to stop the enzyme reaction and stabilize the developed color. The optical density of each well is measured using a wavelength of 450 nm on a microplate reader. Mean absorbance values of each standard are calculated and used to create a standard curve. The standard curve is utilized to determine the IL-18 concentrations of the samples; each sample must be multiplied by the dilution factor to obtain the true concentration. E. Data Entry and Statistical Analysis All data collected was initially recorded on clinical forms and later entered into electronic spreadsheets. A spreadsheet was created specifically for entering the data from each periodontal exam. The periodontal spreadsheet was set up as an electronic periodontal chart into which the values for PD, CAL, BOP, and plaque were entered. Equations were set up within the spreadsheet in order to calculate frequency distributions for the five parameters utilized to characterize periodontal disease status. A master spreadsheet was created which includes patient demographics and clinical information, 23
  32. 32. periodontal disease parameters, CAD, and serum levels of inflammatory mediators. Data was arranged within the master spreadsheet for input and analysis using a statistical software package. Statistical analysis was performed using GraphPad InStat analytical software with a primary aim to evaluate the interrelationships between the inflammatory mediators IL- 18 and CXCL 16 and periodontal disease. Secondary aims were to evaluate the relationship between the aforementioned inflammatory mediators and CAD, in addition to the direct relationship between periodontal disease and CAD. Five periodontal parameters were analyzed as frequency distributions including the following: percent of sites with PD ≥ 5 mm and ≥ 7 mm, percent of sites with CAL ≥ 3 mm and ≥ 5 mm, and percent of sites with BOP. The two thresholds set for PD (≥ 5 mm, ≥ 7 mm) and CAL (≥ 3 mm, ≥ 5 mm) represent moderate and severe disease. Frequency distribution represents extent of disease. Utilizing frequency distributions provided a set of continuous variables for each periodontal parameter within the study population. Serum levels of inflammatory mediators were recorded as raw values, although log values were also calculated and used in statistical analysis. Coronary artery disease status was classified according to the presence and percent of vessel occlusion; patients with vessels having less than 50% occlusion were categorized as non-obstructive CAD while those having vessels with 50% or greater occlusion were categorized as CAD. Patients with CAD were further categorized according to the number of vessels affected. For statistical calculations, CAD status was ranked as follows: 0= no CAD, 1= non-obstructive CAD, 2= 1-vessel obstructive CAD, 3= 2-vessel obstructive CAD, 4= 3-vessel obstructive CAD. 24
  33. 33. Spearman rank correlation, a non-parametric univariate analysis, was performed to analyze the association between levels of inflammatory mediators and individual periodontal disease parameters. The analysis was also perfomed to analyze the association between periodontal disease and CAD. A non-parametric statistical analysis was chosen due to the relatively small sample size and because the data characterizing periodontal disease and CAD did not exhibit a normal distribution. The univariate analyses of the periodontal disease parameters and serum levels of inflammatory mediators, however, do not take into account the effect of other parameters known to influence inflammation and the disease processes including BMI, smoking, diabetes, and statin use. In order to evaluate the effect of periodontal disease on inflammation and CAD while simultaneously accounting for other factors known to contribute to the disease process, multiple regression analyses were performed. The variables analyzed as outcomes include serum levels of IL-18 and CXCL16 as well as CAD status. Variables included in the regression equation include the following: age, male gender, BMI, race, smoking, statin use, each of the five outlined periodontal disease parameters, CAD (when analyzing IL-18 and CXCL16), and serum levels of IL-18 and CXCL16 (when analyzing CAD). 25
  34. 34. III. RESULTS A. Patient Recruitment and Demographics Complete data sets were obtained and analyzed for 51 patients, although 55 patients received a periodontal exam. Four out of the 55 patients who received a periodontal exam did not have a blood sample available for cytokine analysis. Two patients experienced complications during the cardiac catheterization and a blood sample could not be collected. The other two patients’ blood samples were collected, but were not delivered to the research laboratory for storage and cytokine analysis. Of the 51 patients 24 were Caucasian, non-Hispanic (47%), 22 were Hispanic (43%), and 5 were African-American (10%) (Table 1). The patient age range was 30 to 78 years with an average age of 55.43 years. B. Clinical Characteristics In addition to patient demographics, multiple clinical cardiovascular parameters were evaluated prior to cardiac catheterization. Evaluation of smoking status revealed that approximately half (49%) of the patients had never smoked, while 13.7% had quit more than one year prior and 11.8% had quit one month to one year prior to cardiac catheterization. Approximately one quarter (25.5%) of the patient population were active smokers at the time of cardiac catheterization. More than half of the patients (56.8%) were on statin therapy. The average body mass index was 34.66 kg/m2 with a range of 19.15 to 56.09 kg/m2 . A large percentage of the patient population had type 2 diabetes, 60.8%. The average hemoglobin A1c value was 7.11% indicating a fair level of control, 26
  35. 35. although the range was 4.90% to 14.70% demonstrating a great variability of glycemic control within the population. C. Coronary Artery Disease Status Patients were categorized according to their coronary artery disease (CAD) status into five groups (Table 2). The majority of the patients (66.7%) exhibited some degree of CAD, either obstructive or non-obstructive. Non-obstructive CAD was defined as less than 50% occlusion of any number of coronary arteries. Coronary artery disease was considered present if at least 50% occlusion of a vessel was evident at cardiac catheterization and was categorized according to the number of vessels affected. Results of cardiac catheterization are as follows: 33.3% had no CAD, 13.7% had non-obstructive CAD, 9.8% had 1-vessel obstructive CAD, 15.7% had 2-vessel obstructive CAD, and 27.5% had 3-vessel obstructive CAD. D. Periodontal Disease Status Periodontal disease was categorized by both extent and severity (Table 3). Overall the prevalence of severe disease was relatively low in the patient population. Probing depth was analyzed as the percent of sites with values ≥ 5 mm and ≥ 7 mm. The average percentage of sites with PD ≥ 5 mm was 12.7% with a range of 0-76.2% and the average percentage of sites with PD ≥ 7 mm was 2.5% with a range of 0-42.9%. Clinical attachment loss was analyzed as the percent of sites affected; thresholds used included CAL ≥ 3 mm and ≥ 5 mm. The average percentage of sites with CAL ≥ 3 mm was 53.5% with a range of 3.7-100% and the average percentage of sites with CAL ≥ 5 mm was 19.7% with a range of 0-92.1%. 27
  36. 36. According to the American Academy of Periodontology (AAP), periodontal disease is classified according to severity of clinical attachment loss. Moderate disease is defined as 3-4 mm of attachment loss, while severe disease is defined as ≥5 mm of attachment loss. In following the definition of disease endorsed by the AAP, generalized moderate disease was relatively prevalent in the study population. Alternatively, epidemiologic research focusing on the systemic effect of periodontal disease has often utilized extent of disease as a primary parameter. The rationale is that the systemic effect of periodontal disease depends upon the level of exposure; thus more extensive disease will have increased systemic involvement, while minimally extensive disease will have little to no systemic effect. Beck and colleagues diagnosed periodontitis by presense of CAL ≥3 mm and utilized the extent of disease to define severity as follows: <10% none or mild, 10% to <30% moderate, and ≥ 30% severe (Beck 2001). According to the aforementioned definition of disease, the current study population overall was affected with severe disease as evidenced by an average extent of CAL ≥3 mm of 53.5%. Bleeding on probing was dichotomized according to presence or absence and analyzed according to the percentage of sites affected. The average percent of sites with BOP was 23.4% with a range of 1.2-82.7%. Bleeding on probing was utilized as an indicator of active inflammation within the periodontal tissues. The large range demonstrates some patients had a minimal extent, while others had more generalized inflammation. Overall the inflammatory status of the patient population, evidenced by the extent of bleeding on probing, was moderate. 28
  37. 37. TABLE 1 SUMMARY STATISTICS Total patients 51 Average age (years) 55.43 (SD=9.617, range 30-78) Race Caucasian, non-Hispanic 47% (n=24) Hispanic 43% (n=22) African-American 10% (n=5) Average body mass index (kg/m2) 34.66 (SD=8.457, SEM=1.184, range=19.15-56.09) Smoking status Never-smoked 49% (n=25) Quit >1 year prior 13.7% (n=7) Quit 4 weeks-1 year prior 11.8% (n=6) Active smoker 25.5% (n=13) Statin use 56.8% (n=29) Diabetes 60.8% (n=31) Average HbA1c 7.11% (SD=2.073, SEM=0.3723, range=4.90-14.70) 29
  38. 38. TABLE 2 CORONARY ARTERY DISEASE STATUS Coronary artery disease (CAD) categories % patient population No CAD 33.3% (n=17) Non-obstuctive CAD (<50% occlusion, any # vessels) 13.7% (n=7) 1-vessel CAD (>50% occlusion) 9.8% (n=5) 2-vessel CAD (>50% occlusion) 15.7% (n=8) 3-vessel CAD (>50% occlusion) 27.5% (n=14) 30
  39. 39. TABLE 3 PERIODONTAL DISEASE PARAMETERS Periodontal parameter Average % per patient Standard deviation Standard error of mean Range % sites PD ≥ 5 mm 12.7% 17.44 2.44 0 - 76.2% % sites PD ≥ 7 mm 2.5% 6.70 0.94 0 - 42.9% % sites CAL ≥ 3 mm 53.5% 30.82 4.32 3.7 – 100% % sites CAL ≥ 5 mm 19.7% 23.71 3.32 0 - 92.1% % sites with BOP 23.4% 18.68 2.62 1.2 - 82.7% 31
  40. 40. E. Serum Levels of Inflammatory Mediators Serum levels of inflammatory mediators exhibited a large range of values among the patient population (Table 4). Due to the large distribution, log values for the inflammatory mediators were calculated and analyzed in addition to the raw values. The average serum level of IL-18 was 335.92 (pg/mL) with a range of 50-1138. The average serum level of CXCL 16 was 857.22 (ng/mL) with a range of 368-2248. F. Periodontitis and Inflammatory Mediators Univariate Analyses Nonparametric univariate analyses were performed using Spearman Rank Correlation to evaluate the relationships between each periodontal disease parameter and the inflammatory mediators and CAD. Analyzing serum levels of IL-18 in relationship to periodontal parameters revealed a statistically significant correlation with the percent of sites with BOP (p=0.039) (Table 5). None of the other periodontal parameters were significantly related to IL-18. Log transformation of IL-18 values did not change the level of significance for any of the calculations. Analyzing serum levels of CXCL 16 in relation to individual periodontal parameters did not reveal any statistically significant relationships (Table 6). Log transformation of CXCL 16 values did not change the level of significance for any of the calculations. Analysis of CAD status in relation to periodontal parameters did not reveal any statistically significant correlations (Table 7). Multivariate Analyses Multiple regression analyses were performed to evaluate the serum levels of inflammatory mediators and CAD in relation to multiple variables in order to account for confounding factors that may have affected the measured outcomes. Results of analysis 32
  41. 41. of serum IL-18 levels revealed a significant association with statin use (p=0.036), CAL ≥3 mm (p=0.045), and CAL ≥5 mm (p=0.024) (Table 8). Results indicate statin use and periodontal attachment loss are both associated with serum IL-18 levels, however the positive or negative nature of the associations between the variables and outcomes could not be reliably determined due to multicollinearity and resultant wide confidence intervals within the statistical model. The R2 for the multiple regression analysis was 42.45% indicating that 42.45% of the variability among the data is explained by the multiple regression equation. It is important to note there is 57.55% residual variability not explained by the statistical model. Analysis of CXCL16 as the outcome of the multiple regression analysis identified a different relationship with the studied variables (Table 9). CXCL16 levels were significantly related to smoking, PD ≥7 mm, and CAL ≥5 mm. Smoking demonstrated a statistically significant association with CXCL16 levels (p=0.0054). The measures of severe periodontal disease, PD ≥7 mm and CAL ≥5 mm, demonstrated a statistically significant association with CXCL16 (p=0.047 and p=0.040 respectively). Overall, results indicate both smoking and severe periodontal disease were associated with levels of CXCL16. Similarly to multiple regression analysis of IL-18, multicollinearity was also present within this statistical model preventing confident determination of the positive or negative nature of the associations. The R2 for the multiple regression analysis was 65.98% indicating the percentage of the variability among the data explained by the multiple regression equation. Residual variability of 34.02% was not explained by the statistical model. 33
  42. 42. G. Periodontitis and Coronary Artery Disease Univariate Analyses Analysis of individual periodontal disease parameters in relation to CAD status did not identify any statistically significant correlations (Table 7). Multivariate Analyses Multiple regression analysis of CAD revealed a statistically significant association with CAL ≥3 mm (p=0.047) (Table 10). No other statistically significant associations were found between CAD and evaluated parameters. Multicollinearity was again present within the statistical model. Results of the analysis indicate periodontal attachment loss was related to CAD. The R2 for the multiple regression analysis was 54.03% indicating amount of variability among the data explained by the multiple regression equation. Residual variability unexplained by the statistical model was 45.97%. 34
  43. 43. TABLE 4 SERUM LEVELS OF INFLAMMATORY MEDIATORS Inflammatory mediator Average per subject Standard deviation Standard error of mean Range Raw serum levels IL-18 (pg/mL) 335.92 223.85 31.35 50 - 1138 Log values IL-18 (pg/mL) 5.59 0.72 0.10 3.91 - 7.04 Raw serum levels CXCL16 (ng/mL) 857.22 407.08 57.00 368 - 2248 Log values CXCL16 (ng/mL) 6.65 0.45 0.064 5.91 - 7.72 35
  44. 44. TABLE 5 NON-PARAMETRIC UNIVARIATE ANALYSIS OF SERUM LEVELS OF IL-18 AND PERIODONTAL PARAMETERS (Spearman Rank Correlation) Periodontal parameter r value 95% confidence interval Two-tailed P value % sites with PD ≥5 mm 0.14 -0.15 – 0.40 0.34 % sites with PD ≥7 mm 0.073 -0.21 – 0.35 0.61 % sites with CAL ≥3 mm -0.0015 -0.28 – 0.28 0.99 % sites with CAL ≥5 mm -0.015 -0.30 – 0.27 0.92 % sites with BOP 0.29 0.0074 – 0.53 0.039* *statistically significant 36
  45. 45. TABLE 6 NON-PARAMETRIC UNIVARIATE ANALYSIS OF SERUM LEVELS OF CXCL 16 AND PERIODONTAL PARAMETERS (Spearman Rank Correlation) Periodontal parameter r value 95% confidence interval Two-tailed P value % sites with PD ≥5 mm 0.010 -0.27 – 0.29 0.94 % sites with PD ≥7 mm 0.099 -0.19 – 0.37 0.49 % sites with CAL ≥3 mm 0.069 -0.22 – 0.35 0.63 % sites with CAL ≥5 mm 0.098 -0.19 – 0.37 0.49 % sites with BOP 0.099 -0.19 – 0.37 0.49 37
  46. 46. TABLE 7 NON-PARAMETRIC UNIVARIATE ANALYSIS OF CORONARY ARTERY DISEASE AND PERIODONTAL PARAMETERS (Spearman Rank Correlation) Periodontal parameter r value 95% confidence interval Two-tailed P value % sites with PD ≥5 mm -0.020 -0.30 – 0.27 0.89 % sites with PD ≥7 mm -0.088 -0.36 – 0.20 0.54 % sites with CAL ≥3 mm 0.19 -0.10 – 0.45 0.19 % sites with CAL ≥5 mm 0.11 -0.19 – 0.38 0.47 % sites with BOP -0.22 -0.47 – 0.075 0.13 38
  47. 47. TABLE 8 MULTIPLE REGRESSION ANALYSIS OF SERUM LEVELS OF IL-18 R2 = 42.45% Variable Coefficient Standard error 95% confidence interval t ratio P value Constant 1001.50 684.17 -442.11 – 2445.10 1.46 0.16 Age 2.48 6.21 -10.63 – 15.59 0.40 0.69 Male 168.12 123.32 -92.08 – 428.32 1.36 0.19 BMI -12.50 9.52 -32.58 – 7.58 1.31 0.21 Race -12.85 74.72 -170.51 – 144.81 0.17 0.87 CRF-smoking 55.75 59.00 -68.75 – 180.24 0.95 0.36 CAD 49.63 39.66 -34.06 – 133.31 1.25 0.23 Statin use -338.50 148.71 -652.29 – 24.72 2.28 0.036* HbA1c -52.96 36.63 -130.24 – -24.33 1.45 0.17 % sites with PD ≥5 mm 3.48 5.94 -9.05 – 16.01 0.59 0.57 % sites with PD ≥7 mm -10.91 9.67 -31.32 – 9.49 1.13 0.27 % sites with CAL ≥3 mm -7.47 3.45 -14.76 – -0.18 2.16 0.045* % sites with CAL ≥5 mm 10.57 4.27 1.56 – 19.58 2.48 0.024* % sites with BOP 4.32 5.16 -6.58 – 15.21 0.84 0.41 *statistically significant 39
  48. 48. TABLE 9 MULTIPLE REGRESSION ANALYSIS OF SERUM LEVELS OF CXCL 16 R2 = 65.98% Variable Coefficient Standard error 95% confidence interval t ratio P value Constant 944.06 882.36 -917.72 – 2805.80 1.07 0.30 Age -10.43 8.01 -27.33 – 6.48 1.30 0.21 Male -42.19 159.04 -377.77 – 293.39 0.27 0.79 BMI 25.43 12.28 -0.47 – 51.33 2.07 0.054 Race 24.26 96.37 -179.08 – 227.59 0.25 0.80 CRF- smoking -242.39 76.09 -402.95 - -81.83 3.19 0.0054* CAD -26.19 51.15 -134.11 – 81.74 0.51 0.62 Statin use 58.28 191.79 -346.41 – 462.96 0.30 0.76 HbA1c 10.51 47.24 -89.17 – 110.18 0.22 0.83 % sites with PD ≥5 mm -12.54 7.66 -28.70 – 3.62 1.64 0.12 % sites with PD ≥7 mm -26.66 12.47 -52.97 - -0.34 2.14 0.047* % sites with CAL ≥3 mm 2.36 4.46 -7.04 – 11.75 0.53 0.60 % sites with CAL ≥5 mm 12.25 5.51 0.63 – 23.87 2.22 0.040* % sites with BOP -1.94 6.66 -15.99 – 12.10 0.29 0.77 *statistically significant 40
  49. 49. TABLE 10 MULTIPLE REGRESSION ANALYSIS OF CORONARY ARTERY DISEASE R2 = 54.03% Variable Coefficient Standard error 95% confidence interval t ratio P value Constant 0.23 4.41 -9.11 – 9.58 0.053 0.96 Age -0.025 0.039 -0.11 – 0.057 0.64 0.53 Male -0.62 0.76 -2.23 – 1.00 0.81 0.43 BMI 0.018 0.067 -0.12 – 0.16 0.27 0.79 Race -0.038 0.45 -0.98 – 0.91 0.085 0.93 CRF-smoking -0.56 0.44 -1.49 – 0.37 1.28 0.22 Statin use 1.42 0.96 -0.61 – 3.45 1.49 0.16 HbA1c 0.42 0.21 -0.024 – 0.86 2.01 0.062 % sites with PD ≥5 mm 0.021 0.038 -0.060 – 0.10 0.55 0.59 % sites with PD ≥7 mm -0.040 0.065 -0.18 – 0.098 0.61 0.55 % sites with CAL ≥3 mm 0.045 0.021 0.00064 – 0.089 2.15 0.047* % sites with CAL ≥5 mm -0.044 0.030 -0.11 – 0.019 1.48 0.16 % sites with BOP -0.053 0.029 -0.11 – 0.0079 1.85 0.084 Serum IL-18 0.0018 0.0014 -0.0012 – 0.0047 1.29 0.22 Serum CXCL 16 -0.00072 0.0011 -0.0031 – 0.0016 0.64 0.53 * statistically significant 41
  50. 50. IV. DISCUSSION AND SUMMARY Periodontal disease, like coronary artery disease, is a result of the chronic inflammatory process. Results of this investigation demonstrate an association between clinical parameters of periodontitis and the specific inflammatory mediators IL-18 and CXCL16. Interleukin-18 and CXCL16 are associated with CAD as well; however, their specific roles in the disease process are not yet fully understood. IL-18 is a pro- inflammatory cytokine involved in chronic inflammation. It has been identified within human atherosclerotic lesions and is also present in diseased periodontal tissue. Much less is known about the chemokine CXCL16. It is expressed in human atherosclerotic lesions, although emerging evidence suggests it may have atheroprotective functions. Research has also implicated CXCL16 in the pathogenesis of periodontal disease. CXCL16 has been identified within diseased periodontal tissues and is expressed by human gingival fibroblasts. The relationships between parameters of periodontal disease and the measured outcomes, serum levels of IL-18 and CXCL16 and CAD, were evaluated using both univariate and multivariate analyses. Univariate analyses identified a significant correlation between serum IL-18 and the extent of BOP; no other statistically significant correlations were found among the evaluated variables and outcomes. The correlation between IL-18 and the extent of BOP supports the hypothesis that periodontal inflammation is associated with increased systemic inflammation. The relationship between IL-18 and BOP was no longer evident, however, when multiple regression analysis was performed. The dissolution of the relationship can be explained by the effect of confounding factors. Confounding factors, including smoking and diabetes, 42
  51. 51. were prevalent among our patient population. In contrast, multiple regression analysis identified a statistically significant association between periodontal disease and both inflammatory mediators as well as CAD. Three multiple regression analyses were performed analyzing IL-18, CXCL16, and CAD as outcomes. When evaluating an outcome known to be affected by multiple variables, a multiple regression analysis provides better statistical strength as it analyzes the effect of multiple variables in relation to each other. When evaluating serum IL-18 levels, a statistically significant association was found between IL-18 and both threshold measures of CAL. Analysis of serum CXCL16 also identified a statistically significant association with periodontal disease; however, the relationship was slightly different. The two variables reflecting severe periodontitis, PD ≥7 mm and CAL ≥5 mm, were associated with CXCL16 levels. Analysis of CAD identified a statistically significant association with CAL ≥3 mm. Results support the research hypothesis and thus demonstrate and association between periodontal destruction, systemic inflammation, and coronary artery disease. The individual relationships between each inflammatory mediator and periodontal disease, however, are different. IL-18 was related to moderate and severe loss of clinical attachment, while CXCL16 was only associated with measures of severe disease. Determination of the positive or negative nature of the associations between the outcomes and variables included in the multiple regression analysis was an important issue encountered during the study. Placing both CAL ≥3 mm and ≥5 mm within the analyses resulted in counting the CAL ≥5 mm category twice, as CAL ≥3 mm includes those measurements greater than 5 mm. A similar situation was encountered for PD 43
  52. 52. measurement. Additionally, PD and CAL often correlate with each other. With the exception of psuedopocketing and recession, CAL is generally present when a deep PD exists at a site. Essentially four measures of periodontal disease status were included in the multiple regression analysis. Inclusion of four independent variables representing periodontal disease resulted in multicollinearity within the statistical model. Due to multicollinearity, the confidence intervals of periodontal disease variables were wide; thus determination of the nature of the associations, either positive or negative, was unreliable. Solutions to minimize the impact of multicollinearity on the results of multiple regression analyses include removing variables that provide redundant information or increasing sample size. While placing two measures for both PD and CAL in the multiple regression analysis does provide some redundant information, it also allows categorization of patients into moderate and severe disease categories. One solution could be to combine PD and CAL in categorization of disease creating two variables instead of four. A significant controversy within periodontal research involves the definition of periodontal disease. While probing depth and bleeding on probing can be considered measures of active disease and inflammation, they do not provide much information on past history of disease. Conversely, clinical attachment loss is a commonly utilized measure of inflammatory periodontal disease; however, it provides no information regarding current disease activity or inflammatory status. Ideally periodontal disease is diagnosed by assessing the simultaneous occurrence of multiple clinical factors present within a patient. Traditional measures of periodontal disease utilized in clinical practice to diagnose patients include clinical attachment loss, probing depth, bleeding on probing, 44
  53. 53. and radiographic alveolar bone loss. When evaluating patients in an epidemiologic research study however, examination and diagnosis of patients following traditional methods is not generally feasible due to financial and time constraints. Clinical attachment loss does, however, provide information regarding past disease activity assuming the loss of attachment was a result of inflammation. While periodontal attachment loss is generally a sequela of the local inflammatory process, it is intuitive that minimally extensive CAL is likely not associated with generalized severe inflammation. Evidence from epidemiologic studies has clearly shown that patients with regular dental care and minimal inflammation can lose periodontal attachment in the form of marginal soft tissue recession (Loe 1978). Results from our study show the most prevalent periodontal disease parameter was CAL ≥3 mm. In an adult population with an average age of approximately 55 years, some level of clinical attachment loss can be expected in every individual regardless of whether they have a significant history of inflammatory periodontal disease. Results of the multiple regression analysis reveal a significant relationship between each of the three outcome variables and CAL. Although, statistically, the relationship between these parameters was found to be significant, a possibility exists that the relationship was found because CAL ≥3 mm had a high prevalence within the study population. Conversely, analyzing CAL by its extent rather than using patient average values strengthens the association. The relationship demonstrated by the statistical analyses relates extent of disease, in the form of CAL, to the outcome measures. It is less likely that a patient with a negative history of significant inflammatory periodontal disease would have very extensive CAL. 45
  54. 54. It is interesting to note that complete edentulism has been significantly associated with coronary artery disease in multiple studies. In a study of males with and without CAD, CAD was significantly more prevalent among edentulous as compared to dentate patients (Pussinen 2003). Additionally, in a group of 256 patients referred for open heart surgery, 35% were edentulous as compared to 15% of age- and sex-matched controls with no history of CAD (p <0.001) (Meurman 2003). Tooth loss is not an uncommon sequela of the various forms of dental disease; complete edentulism may in fact reflect a history of extensive, severe periodontal disease. Extensive CAL has also been associated with symptomatic CAD in the literature. An investigation comparing the periodontal status of patients with acute coronary syndrome (ACS) versus stable patients undergoing diagnostic coronary angiography identified a positive correlation between the extent of CAL ≥5 mm and the severity of CAD in asymptomatic patients (Gotsman 2007). Compared to patients with mild CAD, patients with severe CAD exhibited increased periodontal destruction, in the form of more extensive clinical attachment loss. Patients with ACS had characteristics consistent with active periodontal infection and inflammation. Effectually the loss of clinical attachment observed as a result of periodontitis represents an accumulation of insults upon the periodontium, just as atherosclerosis may be considered an adverse outcome related to local vascular environmental insults. Suggestions for future research would include utilization of combined measures of periodontal disease to categorize patients. Combining measures of periodontal disease would allow for more definitive identification of patients with periodontal disease. For example, it would be less controversial as to whether a patient is affected with 46
  55. 55. periodontal disease if he or she had both CAL and deep PD. Additionally, composite measures could be developed, in a similar manner to that proposed by Lynch and colleagues (2006), including not only PD and CAL but also BOP and alveolar bone levels. Another suggestion for future research would include an increased sample size to both minimize the impact of multicollinearity and allow analysis of smaller differences within the patient population. Another method to limit the effect of multicollinearity is to reduce the number of independent variables in the multiple regression analysis. As CAD and periodontitis are both multifactorial diseases, removing variables from the analysis, which are known to contribute to the etiology of both disease processes, would weaken the results. Additionally, IL-18 and CXCL16 are novel cytokines meaning they have been more recently discovered and information regarding their normal distribution within a patient population is not available. Since little is known regarding distributions of IL- 18 and CXCL16, a power analysis was not performed to determine the target sample size. However, once more is known about IL-18 and CXCL16 a power analysis would be beneficial in designing future research studies. The effects of chronic inflammation in the body are generally not clinically evident until an acute exacerbation of the disease occurs. For example, myocardial infarction is a significant acute outcome of the chronic inflammatory disease of atherosclerosis. Current research aims to explore the association between inflammation and CAD. Although analysis of the relationships between IL-18, CXCL16 and CAD was not one of the outlined research objectives, they were evaluated in the multiple regression analyses. Review of the available evidence has demonstrated a relationship between the studied inflammatory mediators and CAD. IL-18 has been identified in human 47
  56. 56. atheromas and correlated with atherosclerotic plaque ulcerations as well as clinical symptoms (Gerdes 2002, Mallat 2001). Additionally increased serum IL-18 levels have been identified in patients with acute coronary syndrome. Although CXCL16 is known to mediate cellular processes involved in atherosclerosis, there is a paucity of human data available regarding the nature of its association with CAD. While CXCL16 has been identified in human atheroma specimens, conflicting evidence suggests it may be atheroprotective (Aslanian 2006, Sheikine 2006). Multiple regression analysis of the data in this research study found no association between either IL-18 or CXCL16 and CAD. It is important to note the difference between the patient populations in this research study versus those in the aforementioned studies. Our patient population consisted of stable patients who were not experiencing acute coronary syndrome, ergo coronary angiography provided an analysis of the chronic effect of CAD (atherosclerosis). Since different inflammatory mediators are involved in mediating chronic and acute inflammation, results from studies measuring chronic versus acute outcomes may not be comparable. In addition, when IL-18 and CXCL16 have been correlated with CAD, the studies were evaluating local levels of the inflammatory mediators within atherosclerotic lesions. The local and systemic inflammatory profiles may not coincide in patients with atherosclerosis not experiencing acute symptoms. Finally, the small sample size in this research study would be unable to identify relatively small differences if they existed. While the effects of chronic periodontitis may result in periodontal abscess formation and tooth loss, the disease does not have the same associated morbidity and mortality as CAD. It is unlikely that periodontal inflammation will directly precipitate an 48
  57. 57. adverse cardiovascular event such as a myocardial infarction. However, in patients who are at risk for or are affected with coronary artery disease, minimizing exposure to factors that may contribute to or exacerbate the ongoing disease process is important in prevention of disease progression. Although a certain level of skepticism is necessary when evaluating the results of this and other cross-sectional studies which aim to establish a relationship between one variable and a multi-factorial disease such as CAD, the statistical analyses performed in this study demonstrate a significant relationship between measures of periodontitis and systemic inflammation. While the results of this research study do not provide unequivocal information regarding the complex relationship, they do contribute to the body of knowledge and may provide a basis for future investigations. 49
  58. 58. LITERATURE CITED American Academy of Periodontology Academy Report. Informational Paper: The pathogenesis of periodontal diseases. J Periodontol 1999;70:457-470. Aimetti M, Roman F, Nessi F. Microbiologic analysis of periodontal pockets and carotid atheromatous plaques in advanced chronic periodontitis patients. J Periodontol 2007;78:1718-1723. Albandar J, Brunelle J, Kingman A. Destructive periodontal disease in adults 30 years of age and older in the United States, 1988-1994. J Periodontol 1999;70:13-29. Aslanian A, Charo I. Targeted disruption of the scavenger receptor and chemokine CXCL16 accelerates atherosclerosis. Circulation 2006;114:583-590. Beck J, Elter J, Heiss G, Couper D, Mauriello S, Offenbacher S. Relationship of periodontal disease to carotid artery intima-media wall thickness. Arterioscler Thromb Vasc Biol 2001;21:1816-1822. Beck JD, Offenbacher S. Systemic effects of periodontitis: epidemiology of periodontal disease and cardiovascular disease. J Periodontol 2005;76:2089-2100. Chandrasekar B, Mummidi S, Valente AJ, Patel DN, Bailey SR, Freeman GL, Hatano M, Tokuhisa T, Jensen LE. The proatherogenic cytokine interleukin-18 induces CXCL16 expression in rat aortic smooth muscle cells via MyD88, interleukin-1 receptor-associated kinase, tumor necrosis factor receptor associated factor 6, c-Src, phosphatidylinositol 3- kinase, Akt, c-Jun N-terminal kinase, and activator protein-1 signaling. J Biol Chem 2005;280(28):26,263-26,277. Cirelli J, Park C, Mackool K, Taba M Jr, Lustig K, Burstein H, Giannobile W. AAV2/1- TNFR:Fc gene delivery prevents periodontal disease progression. Gene Ther advance online publication 2008 Dec 11 (DOI 10.1038/gt.2008.174 original article) Claffey N, Nylund K, Kiger R, Garrett S, Egelberg J. Diagnostic predictability of scores of plaque, bleeding, suppuration, and probing depth for probing attachment loss. J Clin Periodontol 1990;17:108-114. D’Aiuto F, Parkar M, Nibali L, Suvan J, Lessem J, Tonetti MS. Periodontal infections cause changes in traditional and novel cardiovascular risk factors: results from a randomized controlled clinical trial. Am Heart J 2006;151:977-984. D’Aiuto R, Ready D, Tonetti MS. Periodontal disease and C-reactive protein-associated cardiovascular risk. J Periodont Res 2004;39:236-241. 50
  59. 59. Daly CG, Mitchell DH, Highfield JE, Grossberg DE, Stewart D. Bacteremia due to periodontal probing: a clinical and microbiological investigation. J Periodontol 2001;72:210-214. Delaleu N, Bickel M. Interleukin-1 beta and interleukin-18: regulation and activity in local inflammation. Periodontology 2000 2004;35:42-52. Delima A, Oates T, Assuma R, Schwartz Z, Cochran D, Amar S, Graves D. Soluble antagonists to interleukin-1 (IL-1) and tumor necrosis factor (TNF) inhibits loss of tissue attachment in experimental periodontitis. J Clin Periodontol 2001;28:233-240. Dongari-Bagtzoglou A, Ebersole J. Increased presence of interleukin-6 (IL-6) and IL-8 secreting fibroblast subpopulations in adult periodontitis. J Periodontol 1998;69:899- 910. Duarte PM, de Mendonca AC, Maximo MBB, Santos VR, Bastos MF, Nociti FH Jr. Effect of anti-infective mechanical therapy on clinical parameters and cytokine levels in human peri-implant diseases. J Periodontol 2009;80:234-243. Engebretson SP, Grbic JT, Singer R, Lamster IB. GCF IL-1β profiles in periodontal disease. J Clin Periodontol 2002;29:48-53. Erren M, Reinecke H, Junker R, Fobker M, Schulte H, Schurek J, Kropf J, Kerber S, Breithardt, Assmann G, Cullen P. Systemic inflammatory parameters in patients with atherosclerosis of the coronary and peripheral arteries. Arterioscler Throm Vasc Biol 1999;19:2355-2363. Figueredo C, Rescala B, Teles R, Teles F, Fischer R, Haffajee A, Socransky S, Gustafsson A. Increased interleukin-18 in gingival crevicular fluid from periodontitis patients. Oral Microbiol Immunol 2008;23:173-176. Gemmell E, Seymour GJ. Immunoregulatory control of Th1/Th2 cytokine profiles in periodontal disease. Periodontology 2000 2004;35:21-41. Geerts SO, Nys M, De Mol P, Charpentier J, Alber A, Legrand V, Rompen EH. Systemic release of endotoxins induced by gentle mastication: association with periodontitis severity. J Periodontol 2002;73:73-78. Geismar K, Stoltze K, Sigurd B, Gyntelberg F, Holmstrup P. Periodontal disease and coronary heart disease. J Periodontol 2006;77:1547-1554. Gerdes N, Sukhova GK, Libby P, Reynolds RS, Young JL, Schonbeck U. Expression of interleukin (IL)-18 and functional IL-18 receptor on human vascular endothelial cells, smooth muscle cells, and macrophages: implications for atherogenesis. J Exp Med 2002;195:245-257. 51
  60. 60. Gotsman I, Lotan C, Soskolne WA, Rassovsky S, Pugatsch T, Lapidus L, Novikov Y, Masrawa S, Stabholz A. Periodontal destruction is associated with coronary artery disease and periodontal infection with acute coronary syndrome. J Periodontol 2007;78:849-858. Gracie JA, Robertson SE, McInnes I. Interleukin-18. J Leukoc Biol 2003;73:213-224. Graves D, Delima A, Assuma R, Amar S, Oates T, Cochran D. Interleukin-1 and tumor necrosis factor antagonists inhibit the progression of inflammatory cell infiltration toward alveolar bone in experimental periodontitis. J Periodontol 1998;69:1419-1425. Greenstein G. The role of bleeding upon probing in the diagnosis of periodontal disease. A literature review. J Periodontol 1984;55:684-688. Hamedi M, Belibasakis G, Cruchley A, Rangarajan M, Curtis M, Bostanci N. Porphyromonas gingivalis culture supernatants differentially regulate interleukin-1beta and interleukin-18 in human monocytic cells. Cytokine 2008;45(2):99-104. Haraszthy V, Zambon J, Trevisan M, Zeid M, Genco R. Identification of periodontal pathogens in atheromatous plaques. J Periodontol 2000;71:1554-1560. Hosokawa Y, Hosokawa I, Ozaki K, Nakae H, Matsuo T. CXC chemokine ligand 16 in periodontal diseases: expression in diseased tissues and production by cytokine- stimulated human gingival fibroblasts. Clin Exp Immunol 2001;149:146-154. Iwamoto Y, Nishimura F, Soga Y, Takeuchi K, Kurihara M, Takashiba S, Murayama Y. Antimicrobial periodontal treatment decreases serum C-reactive protein, tumor necrosis factor-alpha, but not adiponectin levels in patients with chronic periodontitis. J Periodontol 2003;74:1231-1236. Johnson RB, Serio FG. Interleukin-18 concentrations and the pathogenesis of periodontal disease. J Periodontol 2005;76:785-790. Kent LW, Rahemtull F, Michalek SM. Interleukin (IL)-1 and Porphyromonas gingivalis lipopolysaccharide stimulation of IL-6 production by fibroblasts derived from healthy or periodontally diseased human gingival tissue. J Periodontol 1999;70:274-282. Kiechl S, Egger G, Mayr M, Wiedermann C, Bonora E, Oberhollenzer F, Muggeo M, Zu Q, Wick G, Poewe W, Willeit J. Chronic infections and the risk of carotid atherosclerosis: prospective results from a large population study: Circulation 2001;103(8):1064-1070. Kramer J, Gaffen S. Interleukin-17: a new paradigm in inflammation, autoimmunity, and therapy. J Periodontol 2007;78:1083-1093. 52
  61. 61. Lester S, Bain J, Johnson R, Serio F. Gingival concentrations of interleukin-23 and -17 at healthy sites and at sites of clinical attachment loss. J Periodontol 2007;78:1545-1550. Linden G, McClean K, Young I, Evans A, Kee F. Persistently raised C-reactive protein levels are associated with advanced periodontal disease. J Clin Periodontol 2008;35:741- 747. Liu R, Cao C, Meng H, Gao Y. Polymorphonuclear neutrophils and their mediators in gingival tissues from generalized aggressive periodontitis. J Periodontol 2001;72:1545- 1553. Loe H, Anerud A, Boysen H, Smith M. The natural history of periodontal disease in man. The rate of periodontal destruction before 40 years of age. J Periodontol 1978;49:607-620. Loos BG. Systemic markers of inflammation in periodontitis. J Periodontol 2005; 76(11 suppl):2106-2115. Loos BG, Craandijk J, Hoek FJ, Wertheim-van Dillen PME, van der Velden U. Elevation of systemic markers related to cardiovascular diseases in the peripheral blood of periodontitis patients. J Periodontol 2000;71:1528-1534. Lowe GDO. The relationship between infection, inflammation, and cardiovascular disease: an overview. Ann Periodontol 2001;6:1-8. Lynch S, Lavin P, Genco R, Beasley W, Wisner-Lynch L. New composite endpoints to assess efficacy in periodontal therapy clinical trials. J Periodontol 2006; 77: 1314-1322. Mallat Z, Corbaz A, Scoazec A, Besnard S, Leseche G, Chratchko Y, Tedgui A. Expression of interleukin-18 in human atherosclerotic plaques and relation to plaque instability. Circulation 2001;104:1598-1603. Malthaner S, Moore S, Mills M, Saad R, Sabatini R, Takacs V, McMahan A, Oates T Jr. Investigation of the association between angiographically defined coronary artery disease and periodontal disease. J Periodontol 2002; 73: 1169-1176 Manoussakis M, Boiu S, Korkolopoulou P, Kapsogeorgou E, Kavantzas N, Ziakas P, Patsouris E, Moutsopoulos H. Rates of infiltration by macrophages and dendritic cells and expression of interleukin-18 and interleukin-12 in the chronic inflammatory lesions of Sjogren’s syndrome: correlation with certain features of immune hyperactivity and factors associated with high risk of lymphoma development. Arthritis Rheum 2007;56:3977-3988. Meurman JH, Avarnstom M, Janket SJ, Nuutinen P. Oral health and health behavior in patients referred for open-heart surgery. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2003;95:300-307. 53
  62. 62. Mosaad Y, Metwally S, Auf F, Abdel-Samee E, el-Deek B, Limon N, el-Chennawi F. Proinflammatory cytokines (IL-12 and IL-18) in immune rheumatic diseases: relation with disease activity and autoantibodies production. Egypt J Immunol 2003;10:19-26. Noack B, Genco RJ, Trevisan M, Grossi S, Zambon JJ, De Nardin E. Periodontal infections contribute to elevated systemic C-reactive protein level. J Periodontol 2001;72:1221-1227. Nonnenmacher C, Stelzel M, Susin C, Sattler AM, Schaefer JR, Maisch B, Mutters R, Flores-de-Jacoby L. Periodontal microbiota in patients with coronary artery disease measured by real-time plymerase chain reaction: a case-control study. J Periodontol 2007;78:1724-1730. Offenbacher S, Collins J, Heasman P. Diagnostic potential of host response mediators. Adv Dent Res 1993;7:175-181. Orozco A, Gemmell E, Bickel M, Symour G. Interleukin-1β, interleukin-12, interleukin- 18 levels in gingival fluid and serum of patients with gingivitis and periodontitis. Oral Microbiol Immunol 2006;21:256-260. Page RC, Schroeder HE. Pathogenesis of inflammatory periodontal disease. Lab Invest 1976;33:235-249. Paraskevas S, Huizinga J, Loos B. A systematic review and meta-analyses on C-reactive protein in relation to periodontitis. J Clin Periodontol 2008;35:277-290. Patel D, Bailey S, Gresham J, Schuchman D, Shelhamer J, Goldstein B, Foxwell B, Stemerman M, Maranchie J, Valente A, Mummidi S, Chandrasekar B. TLR4-NOX4-AP- 1 signaling mediates lipopolysaccharide-induced CXCR6 expression in human aortic smooth muscle cells. Biochem Biophys Res Comm 2006;347:1113-1120. Pearson T, Mensah G, Alexander R, Anderson J, Cannon R, Criqui M, Fadl Y, Fortmann S, Hong Y, Myers G, Rifai N, Smith S, Taubert K, Tracy R, Vinicor F. AHA/CDC scientific statement: markers of inflammation and cardiovascular disease. Circulation 2003;107:499-522. Pussinen PJ, Jousilahti P, Alfthan G, Palosuo T, Asikainen S, Salomaa V. Antibodies to periodontal pathogens are associated with coronary heart disease. Arterioscler Thromb Vasc Biol 2003;23:1250-1254. Ridker P, Rifai N, Stampfer M, Hennekens. Plasma concentration of interleukin-6 and the risk of future myocardial infarction among apparently healthy men. Circulation 2000;101:1767-1772. 54
  63. 63. Ridker P, Rifai N, Pfeffer M, Sacks F, Lepage S, Braunwald E. Elevation of tumor necrosis factor-α and increased risk of recurrent coronary events after myocardial infarction. Circulation 2000;101:2149-2153. Ross R. Atherosclerosis-an inflammatory disease. N Engl J Med 1999;340:115-126. Sanchez-Munoz F, Dominguez-Lopez A, Yamamoto-Furusho J. Role of cytokines in inflammatory bowel disease. World J Gastroenterol 2008;14:4280-4288. Scanlon FP, Faxon DP, Audet AM, Carabello B, Dehmer GJ, Eagle KA, Legako RD, Leon DR, Marray JA, Nissen SE, Pepine CJ, Watson RM. ACC/AHA guidelines for coronary angiography: executive summary and recommendations: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee on Coronary Angiography). Circulation. 1999;99:2345-2357. Scannapieco F, Bush R, Paju S. Associations between periodontal disease and risk for atherosclerosis, cardiovascular disease, and stroke. A systematic review. Ann Periodontol 2003;8:38-53. Schaetzle M, Loe H, Burgin W, Anerud A, Boysen H, Lang NP. Clinical course of chronic periodontitis. J Clin Periodontol 2003;30:887-901. Seinost G, Wimmer G, Skerget M, Thaller K, Brodmann M, Gasser R, Bratschko R, Pilger E. Periodontal treatment improves endothelial dysfunction in patients with severe periodontitis. Am Heart J 2005;149(6):1050-1054. Sheikine Y, Bang C, Nilsson L, Samnegard A, Hamsten A, Jonasson L, Eriksson P, Sirsjo A. Decreased plasma CXCL16/SR-PSOX concentration is associated with coronary artery disease. Atherosclerosis 2006;188:462-466. Sheikine Y, Sirsjo A. CXCL16/SR-PSOX—a friend or foe in atherosclerosis? Atherosclerosis 2008;197(2):487-495. Slade GD, Offenbacher S, Beck JD, Heiss G, Pankow JS. Acute-phase inflammatory response to periodontal disease in the US population. J Dent Res 2000; 79(1):49-57. Socransky S, Haffajee A, Cugini M, Smith C, Kent R Jr. Microbial complexes in subgingival plaque. J Clin Periodontol 1998;25:134-144. Stashenko P, Fujiyoshi P, Obernesser MS, Prostak L, Haffajee AD, Socransky SS. Levels of interleukin IL-1β in tissue from sites of active periodontal disease. J Clin Periodontol 1991;18(7):548-554. Stoll L, Denning G, Weintraub N. Potential role of endotoxin as a pro-inflammatory mediator of atherosclerosis. Arterioscler Thromb Vasc Biol 2004;24:2227-2236. 55
  64. 64. Taylor BA, Tofler GH, Carey HM, Morel-Kopp MC, Philcox S, Carter TR, Elliott MJ, Kull AD, Ward C, Schenck K. Full-mouth tooth extraction lowers systemic inflammatory and thrombotic markers of cardiovascular risk. J Dent Res 2006;85:74-78. Tenger C, Sundborger A, Jawien J, Zhou X. Interleukin-18 accelerates atherosclerosis accompanied by elevation of IFNγ and CXCL16 expression independently of T cells. Arterioscler Thromb Vasc Biol 2005;25:791-796. Tonetti M, D’Aiuto F, Nibali L, Donald A, Storry C, Parkar M, Suvan J, Hingorani A, Vallance P, Deanfield J. Treatment of periodontitis and endothelial function. N Engl J Med 2007;356:911-920. Wuttge DM, Zhou X, Sheikine Y, Wagsater D, Stemme V, Hedin U, Stemme S, Hansson GK, Sirsjo A. CXCL16/SR-PSOX is an interferon-{gamma}-regulated chemokine and scavenger receptor expressed in atherosclerotic lesions. Arterioscler Thromb Vasc Biol 2004;24:750-755. Yucel O, Berker E, Gariboglu S, Otlu H. Interleukin-11, interleukin-1β, interleukin-12 and the pathogenesis of inflammatory periodontal diseases. J Clin Periodontol 2008;35:365-370. Zaremba M, Gorska R, Suwalski P, Kowalski J. Evaluation of the incidence of periodontitis-associated bacteria in the atherosclerotic plaque of coronary blood vessels. J Periodontol 2007;78:322-327. Zernecke A, Weber C. Inflammatory mediators in atherosclerotic vascular disease. Basic Res Cardiol 2005;100:93-101. 56
  65. 65. 57 VITA Rachel Amanda Schallhorn was born on October 28, 1980 to the Reverend Robert and Frances Schallhorn in Chicago, Illinois. Following graduation from Elkhart Memorial High School in 1998, she attended Capital University in Columbus, Ohio where she majored in biology and minored in chemistry. In 2002 she received a Bachelor of Arts degree graduating summa cum laude. After completing her undergraduate education, she attended the University of Michigan School of Dentistry and received a Doctor of Dental Surgery degree in 2006. Dr. Schallhorn entered a three-year periodontics residency program at the University of Texas Health Science Center in San Antonio, Texas in 2006. She was admitted into the University of Texas Graduate School of Biomedical Sciences in San Antonio in 2007.

×