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ARTICLE INFO ABSTRACT
Keywords:
Hemoglobin A1C and aging,
Hemoglobin A1C anti aging tool,
HBA1C,
HBA1C Biomarker
Original Article
BioMedSciDirect
Publications
Introduction
Copyright 2010 BioMedSciDirect Publications IJBMR - ISSN: 0976:6685. All rights reserved.
c
Int J Biol Med Res.2015;6(3):5084-5086
Contents lists available at BioMedSciDirect Publications
Journal homepage: www.biomedscidirect.com
International Journal of Biological & Medical Research
Glycosylated hemoglobin (HbA1c): A Biomarker of Anti Aging
a b c d e f
Bashir Ahmed Dar, Manzoor Ahmed Dar, Sheeba Bashir, Saima Nazir, Shania Bashir, Yawer Bashir
a
Department of Medicine, Melaka Manipal Medical College, Melaka, Malaysia
b
Department of Surgery, Sohar Hospital Oman
c
Srinagar Kashmir
d
Department of Community Medicine GMC Srinagar Kashmir
e
Obstetrics and Gynaecology SKIMS Soura Srinagar Kashmir India
f
Intern oral maxillofacial surgery ITS Dental College greater Noida Delhi (NCR) India
Glycation
Aging is a multi dimensional process of becoming older and
remains one of the most mysterious areas of biological research. It
represents the accumulation of changes in a person over time
[1][2].
It is among the largest known risk factors for most human
diseases.[3] Roughly 100,000 people worldwide die each day of
age-relatedcauses.[4]
Since ageing is a cause or major risk factor of the age related
diseases and mortality, there are growing efforts in ageing
research to slow ageing and extend healthy lifespan. Ageing
processescan be fasterbecause ofaccumulation oftoxic metabolic
products.
These products could be rogue Advanced Glycation end
products formed from reducing sugars such as glucose, that react
non enzymatically with amino groups in proteins, lipids and
nucleicacidsthroughaseriesofreactionsformingSchiffbasesand
AmadoriproductstoproduceAGE.
This process, also known as the Maillard reaction was
described in the early 1900s, when it was noted that amino acids
heated in presence of reducing sugars developed a characteristic
yellowbrowncolour.[5]
These Advanced Glycation end products corrode our body the
same way rust damages metal in a machine. AGEs as they build up
in the body, they bombard the body's cells like a meteor shower
and continue to cause more damage and rusting that becomes
noticedovermanyyears.
This Glycation, make cells stiffer, less pliable and subject to
damage and premature aging. This is one reason why joints,
muscles and tendons become stiff and inflexible over time.
Glycation thus plays an important role in ageing and has been
implicatedinthepathophysiologyofnumberofdiseases
For most people with normal levels of glucose, the Glycation
process is something that happens gradually over the course of a
lifetime, and it's really not that big of a deal, However people with
highsugarlevelsinbodyleadtoquickandmoreformationofAGEs,
thathastensdamagetocellsofbodyandearlyaging.
When you're younger, your body has more resources to ward
off damage, and you're producing more collagen, says New York
and Miami-based dermatologist Fredric Brandt, who in 2007 was
one of the first to launch an anti-aging skin-care line specifically
addressing glycation.When you reach a certain age, these
Glycation products begin to build up at the same time that your
thresholdfordamageisgettinglower.
Glycation is a fact of life. It's happening right now, to all of us. It
can even be measured. There are number of biomarkers shown to
be related with the ageing process. One of these biomarkers is
glycated hemoglobin (HbA1c).The A1C test is based on non-
enzymatic Glycation pathway by hemoglobin's exposure to plasma
glucose. Therefore Glycation measurement can give idea how fast
it is happening in our body to lead to aging and various age related
diseases.
International Journal of
BIOLOGICAL AND MEDICAL RESEARCH
www.biomedscidirect.comInt J Biol Med Res
Volume 6, Issue 2, April 2015
Glycosylated hemoglobin (HbA1c) is a marker of evaluation of long-term glycemic control in
diabetic patients that predict risks for the development and progression of diabetic
complications. The aim of this study is to evaluate the significance of Glycosylated hemoglobin
(HbA1c) in relation to aging. After going through number of research papers have come to
conclusion that such relationship do exist and Glycosylated hemoglobin (HbA1c) does increase
with advancing age independent of glycemia.It also clearly shows association with premature
aging and increased mortality. Review Criteria: We systematically searched number of articles,
webpages, and major textbooks for writing this article. All papers identified were in English
language and full manuscripts. I also searched the reference lists of identified articles for
additional relevant papers A search for reference data for this purpose was also performed
using the Google search engine. In this short review we summarize the findings given by
different researchers on the subject and bring it in our support to prove HBA1C should also be
usedasantiagingtool.
* Corresponding Author : Dr Bashir Ahmed Dar
Associate Professor Medicine
Department of Medicine, Melaka Manipal Medical College
Melaka Malaysia 75150
Email:drbashir123@gmail.com
Copyright 2010 BioMedSciDirect Publications. All rights reserved.c
Bashir Ahmed Dar Int J Biol Med Res. 2015; 6(3): 5084-5086
5085
HemoglobinA1Candaging
The hemoglobin A1C test also called HbA1c, glycated
hemoglobin test, or glycohemoglobin test is an important blood
test used to determine how well diabetes is being controlled.
HemoglobinA1Cprovidesan averageofbloodsugarcontrolovera
sixto12weekperiod.[6]
However, the same blood test also helps identify age-
accelerating Glycation reactions in the body. The hemoglobin A1C
blood test is thus being considered as useful in non-diabetics who
wanttoguardagainstthedestructiveGlycationprocess.
The hemoglobin A1C test identifies the potential for age-
accelerating Glycation reactions in our bodies. However, this
valuable tool has been dramatically underutilized in the context of
aging.
Scientists believe that it is not only those with diabetes or pre-
diabetes who should be concerned about the damaging effects of
Glycation in the body, but all of us should be concerned as the
damage inflicted by advanced Glycation end-products (AGEs) is
moreastheageadvances.
Lydie N. Pani, Leslie Korenda and others published a research
"Effect of Aging on A1C Levels in Individuals without Diabetes
“they found that A1C was associated with age in nondiabetic
subjects and in subjects with normal glucose tolerance (NGT) in
twopopulation-basedcohorts.[7]
They performed cross-sectional analyses of A1C across age
categories in 2,473 nondiabetic participants of the Framingham
Offspring Study (FOS) and in 3,270 nondiabetic participants from
the National Health and Nutrition Examination Survey (NHANES)
2001–2004.The results in their study showed positive association
of AIC with age in nondiabetic subjects. The 97.5th percentiles for
A1C were 6.0% and 5.6% for nondiabetic individuals aged <40
years in FOS and NHANES, respectively, compared with 6.6% and
6.2%forindividualsaged=70years.
They further concluded that the studies that have failed to
demonstrate an association between age and A1C used diagnostic
criteria to exclude diabetes that are now outdated or were small
andpossiblyunderpowered.[8–10]
In another study researchers concluded that Glycemic control
deteriorates with age in healthy, non-diabetic individuals. Age-
related rises in haemoglobin A1C result from a small but steady
declineinpancreaticbetacellfunction.[11]
Similarly Frank Q. Nuttall, in the study found that there was a
modestage-relatedincreasein%HbA1c.[12]
While as in another study on Japanese Population showed the
same results. This study on Japanese population was done to
evaluate whether there is any change in HbA1c with age and to
determine the effects of body mass index (BMI), exercise, and
familyhistoryofdiabetesonthischange.
A cross-sectional survey of 7,664 male Japanese workers aged
20–59 years was performed. All subjects received a physical
examination that included measurement of HbA1c as an indicator
of plasma glucose level. The subjects were classified according to
their ages and BMIs, and any relationship with HbA1c levels was
evaluated.[13]
Results showed that in all BMI groups, HbA1c increased with
age. The greatest increase in HbA1c was observed in the 40 to 49
year-oldage-groupinsubjectswithaBMI=26kg/m2andinthe30
to39yearoldagegroupinsubjectswithaBMI>26.
HbA1c in the subjects aged 20 to 29 years did not change with
BMI. In contrast, HbA1c in subjects aged 30 to 59 years was
significantly higher in those with a BMI >26 when compared with
thosewithBMI=20.
The age dependent increase in HbA1c was greater in subjects
with a positive rather than negative family history of diabetes.
They further concluded that the age dependent increase in HbA1c
maybeaconsequenceoftheagingprocessitself.[13]
Therefore monitoring of hemoglobin A1c levels is essential for
all adults who wish to identify excess glycation processes in their
bodies and take measures to control and minimize glycation
induced damage, as the favourable glucose metabolism and its
control has been identified as a central key factor for longevity.
[14]
A Community-based cross-sectional study involving 2368
subjects aged = 20 years was done from Chandigarh, India and all
had normal glucose tolerance. In this study there was a significant
positive correlation between mean HbA1c and age in these
subjects.
The increase in HbA1c with each advancing year was 0.01%
above the age of 20 years. A significantly higher number (6.5%,
21/325) of subjects had HbA1c of = 6.5% (48 mmol/mol) in those
above the age of 50 years compared with those below the age of 50
years and it was concluded that HbA1c increases with advancing
ageindependentofglycaemia.[15]
A1C levels are positively associated with age in nondiabetic
populations. The age-dependent increase in HbA1c may be a
consequence of the aging process itself independent of glycaemia.
Age therefore should be taken into consideration when using
HbA1c for the diagnosis and management of diabetes and
prediabetes.
The HBA1C test which is being used primarily to monitor
blood sugar control in diabetics also helps to identify the level of
age-acceleratingGlycationinourbody.
Therefore being important factor in aging makes the
hemoglobin HBA1C test important tool for anti aging program to
preventacceleratedagingduetovariousproblems.
HBA1C level is an indirect measure of how fast you are aging
and how much damage is likely being done to your cells by the
agingprocess.
Together with other key anti aging tests, the HBA1C blood test
is a marker for potential accelerated aging, and can help to clear
theproblemsandcomplicationsofhighbloodsugarandGlycation.
Knowing your HBA1C levels and responding accordingly will
ensureamuchlongerandhealthierlife
Conclusions
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Copyright 2010 BioMedSciDirect Publications IJBMR - ISSN: 0976:6685.
All rights reserved.
c
Bashir Ahmed Dar Int J Biol Med Res. 2015; 6(3): 5084-5086

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Research article on anti aging tool by Prof Dr Bashir Ahmed Dar Sopore Kashmir

  • 1. ARTICLE INFO ABSTRACT Keywords: Hemoglobin A1C and aging, Hemoglobin A1C anti aging tool, HBA1C, HBA1C Biomarker Original Article BioMedSciDirect Publications Introduction Copyright 2010 BioMedSciDirect Publications IJBMR - ISSN: 0976:6685. All rights reserved. c Int J Biol Med Res.2015;6(3):5084-5086 Contents lists available at BioMedSciDirect Publications Journal homepage: www.biomedscidirect.com International Journal of Biological & Medical Research Glycosylated hemoglobin (HbA1c): A Biomarker of Anti Aging a b c d e f Bashir Ahmed Dar, Manzoor Ahmed Dar, Sheeba Bashir, Saima Nazir, Shania Bashir, Yawer Bashir a Department of Medicine, Melaka Manipal Medical College, Melaka, Malaysia b Department of Surgery, Sohar Hospital Oman c Srinagar Kashmir d Department of Community Medicine GMC Srinagar Kashmir e Obstetrics and Gynaecology SKIMS Soura Srinagar Kashmir India f Intern oral maxillofacial surgery ITS Dental College greater Noida Delhi (NCR) India Glycation Aging is a multi dimensional process of becoming older and remains one of the most mysterious areas of biological research. It represents the accumulation of changes in a person over time [1][2]. It is among the largest known risk factors for most human diseases.[3] Roughly 100,000 people worldwide die each day of age-relatedcauses.[4] Since ageing is a cause or major risk factor of the age related diseases and mortality, there are growing efforts in ageing research to slow ageing and extend healthy lifespan. Ageing processescan be fasterbecause ofaccumulation oftoxic metabolic products. These products could be rogue Advanced Glycation end products formed from reducing sugars such as glucose, that react non enzymatically with amino groups in proteins, lipids and nucleicacidsthroughaseriesofreactionsformingSchiffbasesand AmadoriproductstoproduceAGE. This process, also known as the Maillard reaction was described in the early 1900s, when it was noted that amino acids heated in presence of reducing sugars developed a characteristic yellowbrowncolour.[5] These Advanced Glycation end products corrode our body the same way rust damages metal in a machine. AGEs as they build up in the body, they bombard the body's cells like a meteor shower and continue to cause more damage and rusting that becomes noticedovermanyyears. This Glycation, make cells stiffer, less pliable and subject to damage and premature aging. This is one reason why joints, muscles and tendons become stiff and inflexible over time. Glycation thus plays an important role in ageing and has been implicatedinthepathophysiologyofnumberofdiseases For most people with normal levels of glucose, the Glycation process is something that happens gradually over the course of a lifetime, and it's really not that big of a deal, However people with highsugarlevelsinbodyleadtoquickandmoreformationofAGEs, thathastensdamagetocellsofbodyandearlyaging. When you're younger, your body has more resources to ward off damage, and you're producing more collagen, says New York and Miami-based dermatologist Fredric Brandt, who in 2007 was one of the first to launch an anti-aging skin-care line specifically addressing glycation.When you reach a certain age, these Glycation products begin to build up at the same time that your thresholdfordamageisgettinglower. Glycation is a fact of life. It's happening right now, to all of us. It can even be measured. There are number of biomarkers shown to be related with the ageing process. One of these biomarkers is glycated hemoglobin (HbA1c).The A1C test is based on non- enzymatic Glycation pathway by hemoglobin's exposure to plasma glucose. Therefore Glycation measurement can give idea how fast it is happening in our body to lead to aging and various age related diseases. International Journal of BIOLOGICAL AND MEDICAL RESEARCH www.biomedscidirect.comInt J Biol Med Res Volume 6, Issue 2, April 2015 Glycosylated hemoglobin (HbA1c) is a marker of evaluation of long-term glycemic control in diabetic patients that predict risks for the development and progression of diabetic complications. The aim of this study is to evaluate the significance of Glycosylated hemoglobin (HbA1c) in relation to aging. After going through number of research papers have come to conclusion that such relationship do exist and Glycosylated hemoglobin (HbA1c) does increase with advancing age independent of glycemia.It also clearly shows association with premature aging and increased mortality. Review Criteria: We systematically searched number of articles, webpages, and major textbooks for writing this article. All papers identified were in English language and full manuscripts. I also searched the reference lists of identified articles for additional relevant papers A search for reference data for this purpose was also performed using the Google search engine. In this short review we summarize the findings given by different researchers on the subject and bring it in our support to prove HBA1C should also be usedasantiagingtool. * Corresponding Author : Dr Bashir Ahmed Dar Associate Professor Medicine Department of Medicine, Melaka Manipal Medical College Melaka Malaysia 75150 Email:drbashir123@gmail.com Copyright 2010 BioMedSciDirect Publications. All rights reserved.c
  • 2. Bashir Ahmed Dar Int J Biol Med Res. 2015; 6(3): 5084-5086 5085 HemoglobinA1Candaging The hemoglobin A1C test also called HbA1c, glycated hemoglobin test, or glycohemoglobin test is an important blood test used to determine how well diabetes is being controlled. HemoglobinA1Cprovidesan averageofbloodsugarcontrolovera sixto12weekperiod.[6] However, the same blood test also helps identify age- accelerating Glycation reactions in the body. The hemoglobin A1C blood test is thus being considered as useful in non-diabetics who wanttoguardagainstthedestructiveGlycationprocess. The hemoglobin A1C test identifies the potential for age- accelerating Glycation reactions in our bodies. However, this valuable tool has been dramatically underutilized in the context of aging. Scientists believe that it is not only those with diabetes or pre- diabetes who should be concerned about the damaging effects of Glycation in the body, but all of us should be concerned as the damage inflicted by advanced Glycation end-products (AGEs) is moreastheageadvances. Lydie N. Pani, Leslie Korenda and others published a research "Effect of Aging on A1C Levels in Individuals without Diabetes “they found that A1C was associated with age in nondiabetic subjects and in subjects with normal glucose tolerance (NGT) in twopopulation-basedcohorts.[7] They performed cross-sectional analyses of A1C across age categories in 2,473 nondiabetic participants of the Framingham Offspring Study (FOS) and in 3,270 nondiabetic participants from the National Health and Nutrition Examination Survey (NHANES) 2001–2004.The results in their study showed positive association of AIC with age in nondiabetic subjects. The 97.5th percentiles for A1C were 6.0% and 5.6% for nondiabetic individuals aged <40 years in FOS and NHANES, respectively, compared with 6.6% and 6.2%forindividualsaged=70years. They further concluded that the studies that have failed to demonstrate an association between age and A1C used diagnostic criteria to exclude diabetes that are now outdated or were small andpossiblyunderpowered.[8–10] In another study researchers concluded that Glycemic control deteriorates with age in healthy, non-diabetic individuals. Age- related rises in haemoglobin A1C result from a small but steady declineinpancreaticbetacellfunction.[11] Similarly Frank Q. Nuttall, in the study found that there was a modestage-relatedincreasein%HbA1c.[12] While as in another study on Japanese Population showed the same results. This study on Japanese population was done to evaluate whether there is any change in HbA1c with age and to determine the effects of body mass index (BMI), exercise, and familyhistoryofdiabetesonthischange. A cross-sectional survey of 7,664 male Japanese workers aged 20–59 years was performed. All subjects received a physical examination that included measurement of HbA1c as an indicator of plasma glucose level. The subjects were classified according to their ages and BMIs, and any relationship with HbA1c levels was evaluated.[13] Results showed that in all BMI groups, HbA1c increased with age. The greatest increase in HbA1c was observed in the 40 to 49 year-oldage-groupinsubjectswithaBMI=26kg/m2andinthe30 to39yearoldagegroupinsubjectswithaBMI>26. HbA1c in the subjects aged 20 to 29 years did not change with BMI. In contrast, HbA1c in subjects aged 30 to 59 years was significantly higher in those with a BMI >26 when compared with thosewithBMI=20. The age dependent increase in HbA1c was greater in subjects with a positive rather than negative family history of diabetes. They further concluded that the age dependent increase in HbA1c maybeaconsequenceoftheagingprocessitself.[13] Therefore monitoring of hemoglobin A1c levels is essential for all adults who wish to identify excess glycation processes in their bodies and take measures to control and minimize glycation induced damage, as the favourable glucose metabolism and its control has been identified as a central key factor for longevity. [14] A Community-based cross-sectional study involving 2368 subjects aged = 20 years was done from Chandigarh, India and all had normal glucose tolerance. In this study there was a significant positive correlation between mean HbA1c and age in these subjects. The increase in HbA1c with each advancing year was 0.01% above the age of 20 years. A significantly higher number (6.5%, 21/325) of subjects had HbA1c of = 6.5% (48 mmol/mol) in those above the age of 50 years compared with those below the age of 50 years and it was concluded that HbA1c increases with advancing ageindependentofglycaemia.[15] A1C levels are positively associated with age in nondiabetic populations. The age-dependent increase in HbA1c may be a consequence of the aging process itself independent of glycaemia. Age therefore should be taken into consideration when using HbA1c for the diagnosis and management of diabetes and prediabetes. The HBA1C test which is being used primarily to monitor blood sugar control in diabetics also helps to identify the level of age-acceleratingGlycationinourbody. Therefore being important factor in aging makes the hemoglobin HBA1C test important tool for anti aging program to preventacceleratedagingduetovariousproblems. HBA1C level is an indirect measure of how fast you are aging and how much damage is likely being done to your cells by the agingprocess. Together with other key anti aging tests, the HBA1C blood test is a marker for potential accelerated aging, and can help to clear theproblemsandcomplicationsofhighbloodsugarandGlycation. Knowing your HBA1C levels and responding accordingly will ensureamuchlongerandhealthierlife Conclusions REFERENCES 1. Bowen, Richard L.; Atwood, Craig S. (2004). "Living and Dying f o r S e x " . G e ro n t o l o g y 5 0 ( 5 ) : 2 6 5 – 9 0 . D o i : 1 0 . 1 1 5 9 / 0 0 0 0 7 9 1 2 5 . P M I D 1 5 3 3 1 8 5 6 http://agingresearch.wisc.edu/pdf/AGING%20THEORY.pdf 2. Birbrair, A.; Zhang, T.; Wang, Z.-M.; Messi, M. L.; Mintz, A.; Delbono, O. (2013). "Type-1 pericytes participate in fibrous tissue deposition in aged skeletal muscle". AJP: Cell Physiology 305 (11): C1098. doi:10.1152/ajpcell.00171.2013. http://ajpcell.physiology.org/content/ajpcell/305/11/C109 8.full.pdf
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