Cardiovascular Biomarkers Lecture

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Cardiovascular Biomarkers Lecture

  1. 1. Biomarkers for Cardiovascular Diseases: Review of Recent Concepts FELIPE S TEMPLO, JR,MD, DPSP ANATOMIC & CLINICAL PATHOLOGY
  2. 2. OBJECTIVE: TO PROVIDE AN OVERVIEW OF RECENT CONCEPTS AND CLINICAL STUDIES OF CARDIOVASCULAR BIOMARKERS.
  3. 3. WHAT IS A BIOMARKER? • A BIOMARKER is measurable and quantifiable biological parameter which serve as indices for health- and physiology-related assessments such as disease risk, psychiatric disorder, environmental exposure and its effects, disease diagnosis, metabolic processes, substance abuse, pregnancy, cell line development, epidemiologic studies, etc (Medical Subject Heading , 1989)
  4. 4. WHAT IS A BIOMARKER? • A BIOMARKER is a characteristic that is objectively measured and evaluated as an indicator or normal biological process, pathogenic process or pharmacologic responses to a therapeutic intervention. These can be measured in a bodily fluid (e.g. blood or urine)or via medical imaging or testing (2001, NIH)
  5. 5. WHAT IS A BIOMARKER? A BIOMARKER can be anything that reflects a biological process-from genetic markers to imaging tests SOLUBLE BIOMARKERS are particularly attractive because they are EASY TO OBTAIN and generally REPRODUCIBLE BIOMARKERS within the cardiovascular field ‘frequently’ refer to circulating molecules in the blood.
  6. 6. WHY THERE ARE INTERESTS IN CARDIOVASCULAR BIOMARKERS FOR PRIMARY PREVENTION? • 1. Advances if genetic and molecular researches • 2. ‘Traditional’ risk factors ( hypertension, smoking, hyperlipidemia and diabetes) do not fully explain interindividual variation in cardiovascular risk.
  7. 7. CHARACTERISTICS OF AN IDEAL (CARDIOVASCULAR) BIOMARKER • 1. It should easily be measured • 2. Provides information that in addition to features that are readily apparent • 3. Assist in the management of the patient
  8. 8. CHARACTERISTICS OF AN IDEAL (CARDIOVASCULAR) BIOMARKER • “ Whether a BIOMARKER is used to screen for a disease, diagnose a disease or inform prognosis, IT SHOULD AFFECT CLINICAL MANAGEMENT”- ( Khot UN, JAMA, 2003)
  9. 9. GENERAL CONSIDERATIONS IN EVALUATING NOVEL BIOMARKERS: • ( 2007,MORROW AND de LEMOS) • 1. Ease of Measurement- existence of standardized and reproducible assays • 2. Addition of Information-incremental information from measuring a biomarker • 3. Effect on Management- clinical trials in primary prevention setting.
  10. 10. STATISTICAL ASSESSMENTS • 1. DISCRIMINATION • 2. CALIBRATION • 3. RECLASSIFICATION
  11. 11. STATISTICAL ASSESSMENTS DISCRIMINATION- is the ability of a biomarker to distinguish those who develop a disease from those who do not. This can be characterized by the area under the ROC curve ( AUC) or the c-statistic SENSTIVITY- true positive rate SPECIFICITY- true negative rate
  12. 12. STATISTICAL ASSESSMENTS • CALIBRATION-refers to the concordance between predicted risk and observed risk assessed by comparing modeled risk estimates with actual event rates
  13. 13. STATISTICAL ASSESSMENTS • RECALIBRATION- refers to the ability of a test to change an individual’s risk classification. It is based on risk categories, it is potentially the most clinically relevant criterion, because treatment decisions are often linked to whether a patient is considered high risk or low risk rather than on their specific predicted event rate.
  14. 14. SELECTIVE BIOMARKERS • 1. HIGH-SENSITIVITY CRP • 2. B-TYPE NATRIURETIC PEPTIDE • 3. LIPOPROTEIN ASSOCIATED PHOSPHOLIPASE A2 • 4. HIGH SENSITIVITY TROPONIN
  15. 15. HIGH SENSITIVITY C-REACTIVE PROTEIN • Originally discovered by Tillett and Francis in 1930. • It was found in the serum of patients with acute inflammation and was noted to react with the C polysaccharide of pneumococcus, • An acute-phase reactant, produced primarily by hepatocytes in response to stimulation from interlukin-6 and tumor necrosis factor. • Typically, binds to phosphocholine expressed on the surface of dead or dying cells and activates the complement system via the C1Q complex .
  16. 16. HIGH SENSITIVITY C-REACTIVE PROTEIN • In general, circulating CRP concentrations can increase up to 50 000–fold in acute inflammation (i.e., infection) within 6 h. • CRP typically peaks at 48 h. Because the half-life of CRP is constant, the degree of increase is determined by the severity of the precipitating cause
  17. 17. HIGH SENSITIVITY C-REACTIVE PROTEIN • In the past 15 years, more than 20 epidemiological studies have demonstrated a significant association between increased CRP concentrations as measured by use of high-sensitivity assays (hs-CRP) and the risk of a first cardiovascular event among asymptomatic patients. • A meta-analysis of 22 studies by the US Preventive Services Task Force indicated that hs-CRP concentrations greater than or equal to 3 mg/L were associated with a 60% increased risk of cardiovascular disease
  18. 18. HIGH SENSITIVITY C-REACTIVE PROTEIN • In the 2010 American College of Cardiology Foundation/American Heart Association Guideline for Assessment of Cardiovascular Risk in Asymptomatic Adults, the measurement of hsCRP in older men and women with LDL 130 mg/Dl to aid in the decision to use statins was given a class Iia recommendation. Overall, measuring hs-CRP for cardiovascular risk assessment in men 50 years and women 60 years was given a class Iib recommendation
  19. 19. B-TYPE NATRIURETIC PEPTIDE • BNP is a member of a family of hormones known as the natriuretic peptides ,synthesized primarily in the heart, and upregulated by myocardial wall stress. • The gene that encodesBNP [natriuretic peptide B (NPPB)3] initially produces preproBNP. • PreproBNP is cleaved to form proBNP, a 108–amino acid peptide precursor.
  20. 20. B-TYPE NATRIURETIC PEPTIDE • proBNP is cleaved by the enzyme corin, forming the biologically active C-terminal fragment (mature BNP) as well as the inactive N-terminal fragment (NTproBNP). • Both BNP and NT-proBNP can be measured in plasma, the latter has a longer half-life (1–2 h, compared with 20 min).
  21. 21. B-TYPE NATRIURETIC PEPTIDE • Both BNP and NT-proBNP are markedly increased in individuals with acute heart failure , which makes them valuable biomarkers in the setting of suspected heart failure. • Framingham Offspring Study, BNP concentrations 20 pg/mL were associated with a 60%–200% increased risk of cardiovascular events, stroke, heart failure, and all-cause mortality during a mean follow-up of 5.2 years
  22. 22. B-TYPE NATRIURETIC PEPTIDE • A recent meta-analysis of 40 prospective studies, approximately half of which were performed in primary prevention populations, found consistently strong associations between BNP concentrations and cardiovascular risk. • Subtle increases in BNP could reflect increased ventricular wall stress resulting from subclinical ischemia, high afterload, or increased neurohormonal activation.
  23. 23. B-TYPE NATRIURETIC PEPTIDE • There are fewer data on whether BNP measurements improve discrimination, calibration, or reclassification for predicting cardiovascular events, on top of traditional risk factors
  24. 24. LIPOPROTEIN-ASSOCIATED PHOSPHOLIPASE A2 • Lp-PLA2 is a 441–amino acid protein, encoded by the phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma) (PLA2G7) gene, which is produced by inflammatory cells. • It circulates mainly with LDL (20% is associated with HDL or remnant lipoproteins),and it is responsible for hydrolyzing oxidized phospholipids in LDL. It catalyzes the degradation(hydrolysis) of platelet activating factor to inactive products .
  25. 25. LIPOPROTEIN-ASSOCIATED PHOSPHOLIPASE A2 • It is highly upregulated in atherosclerotic plaques, and may be directly involved in development of atherosclerosis and plaque rupture. • It is produced by macrophages and foam cells in the vascular intima, Lp-PLA2 is thought to be potentially more specific for vascular inflammation than other inflammatory markers, such as CRP.
  26. 26. LIPOPROTEIN-ASSOCIATED PHOSPHOLIPASE A2 • West of Scotland Coronary Prevention Study study, both hs-CRP and Lp-PLA2 were significantly associated with increased cardiovascular risk. • Atherosclerosis Risk in Communities study, the weighted mean of both Lp-PLA2 and hs-CRP were higher in those who went on to develop coronary events than in those who did not
  27. 27. HIGH-SENSITIVITY TROPONIN • In 1963, Ebashi and colleagues discovered that a new myofibrillar protein, troponin, was integral to both skeletal and cardiac muscle contraction. • Cardiac troponins have become the standard biomarker in the diagnosis of acute myocardial infarction. • A troponin concentration above the 99th percentile (of a healthy population)is considered diagnostic of an acute myocardial infarction.
  28. 28. HIGH-SENSITIVITY TROPONIN • Newer generations of cardiac troponin I and T assays, the so called high-sensitivity assays, permit detection of concentrations significantly lower than the 99th percentile of the normal reference population. • The hstroponin assay, which can detect picomolar concentrations of troponin, has increased the sensitivity of acute myocardial infarction diagnosis and introduced other potential clinical applications
  29. 29. HIGH-SENSITIVITY TROPONIN • 1.de Lemos- hs-troponin T concentrations were associated with baseline structural heart disease and all-cause and cardiovascular mortality over 6 years of follow up • 2. deFilippi-Increased hs-troponin T concentrations were associated with the development of heart failure and cardiovascular death. • 3. Atherosclerosis Risk in Communities study found that hs-troponin T concentrations were associated with incident CHD, mortality, and heart failure in nearly 10000 individuals.
  30. 30. Comparisons of Biomarkers • “NT-proBNP concentrations are more strongly related to future vascular risk than hs-CRP concentrations” • “hs-troponin measurements have predictive value comparable to NT-proBNP and greater than hs-CRP”
  31. 31. Comparisons of Biomarkers 1. BNP and NT-proBNP strongly predict incident heart failure risk. 2. hs-CRP and Lp-PLA2 are very good markers of vascular risk. 3. “Myocardial” biomarkers such as NT-proBNP and hs-troponin are also surprisingly good predictors of future vascular events
  32. 32. Comparisons of Biomarkers “Panels of multiple biomarkers appear superior to individual biomarkers , although the optimal composition of multi-marker panel remains to be established”.
  33. 33. NEW DIRECTIONS • 1. PROTEOMICS • 2. METABOLOMICS • 3. GENE EXPRESSION PROFILING
  34. 34. TAKE HOME MESSAGES 1. Biomarkers hold the promise of earlier and more accurate cardiovascular risk stratification. 2. Their role in acute cardiovascular diseases, such as myocardial infarction and heart failure, has been well studied.
  35. 35. TAKE HOME MESSAGES 4. An increasing number of studies have investigated the role of biomarkers in primary prevention. 5. Future strategies will likely involve larger biomarker panels and more specific target populations. Larger panels require new biomarkers that provide nonoverlapping information to already -available biomarkers or risk factors. Newer, “unbiased” approaches,such as proteomics or metabolomics, show some promise in this regard.
  36. 36. TAKE HOME MESSAGES • 5. No biomarker has emerged as the best screening marker for cardiovascular disease, and it is likely that no single biomarker will be sufficiently sensitive or specific to be used on its own. • 6. Further studies are also needed to better define the target populations for biomarker screening, because a very broad approach maybe unnecessary as many individuals are adequately risk stratified by traditional risk factors.
  37. 37. THANK YOU

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