TY - JOUR
T1 - Epigenetic clock analysis of diet, exercise, education, and lifestyle factors
AU - Quach, Austin
AU - Levine, Morgan E.
AU - Tanaka, Toshiko
AU - Lu, Ake T.
AU - Chen, Brian H.
AU - Ferrucci, Luigi
AU - Ritz, Beate
AU - Bandinelli, Stefania
AU - Neuhouser, Marian L.
AU - Beasley, Jeannette M.
AU - Snetselaar, Linda
AU - Wallace, Robert B.
AU - Tsao, Philip S.
AU - Absher, Devin
AU - Assimes, Themistocles L.
AU - Stewart, James D.
AU - Li, Yun
AU - Hou, Lifang
AU - Baccarelli, Andrea A.
AU - Whitsel, Eric A.
AU - Horvath, Steve
PY - 2017
Y1 - 2017
N2 - Behavioral and lifestyle factors have been shown to relate to a number of health-related outcomes, yet there is a need for studies that examine their relationship to molecular aging rates. Toward this end, we use recent epi genetic biomarkers of age that have previously been shown to predict all-cause mortality, chronic conditions and age-related functional decline. We analyze cross-sectional data from 4,173 postmenopausal female participants from the Women's Health Initiative, as well as 402 male and female participants from the Italian cohort study, Invecchiare nel Chianti. Extrinsic epigenetic age acceleration (EEAA) exhibits significant associations with fish intake (p=0.02), moderate alcohol consumption (p=0.01), education (p=3x10-5), BMI (p=0.01), and blood carotenoid levels (p=1x10-5)-an indicator of fruit and vegetable consumption, whereas intrinsic epigenetic age acceleration (IEAA) is associated with poultry intake (p=0.03) and BMI (p=0.05). Both EEAA and IEAA were also found to relate to indicators of metabolic syndrome, which appear to mediate their associations with BMI. Metformin-the first-line medication for the treatment of type 2 diabetes-does not delay epigenetic aging in this observational study. Finally, longitudinal data suggests that an increase in BMI is associated with increase in both EEAA and IEAA. Overall, the epigenetic age analysis of blood confirms the conventional wisdom regarding the benefits of eating a high plant diet with lean meats, moderate alcohol consumption, physical activity, and education, as well as the health risks of obesity and metabolic syndrome.
AB - Behavioral and lifestyle factors have been shown to relate to a number of health-related outcomes, yet there is a need for studies that examine their relationship to molecular aging rates. Toward this end, we use recent epi genetic biomarkers of age that have previously been shown to predict all-cause mortality, chronic conditions and age-related functional decline. We analyze cross-sectional data from 4,173 postmenopausal female participants from the Women's Health Initiative, as well as 402 male and female participants from the Italian cohort study, Invecchiare nel Chianti. Extrinsic epigenetic age acceleration (EEAA) exhibits significant associations with fish intake (p=0.02), moderate alcohol consumption (p=0.01), education (p=3x10-5), BMI (p=0.01), and blood carotenoid levels (p=1x10-5)-an indicator of fruit and vegetable consumption, whereas intrinsic epigenetic age acceleration (IEAA) is associated with poultry intake (p=0.03) and BMI (p=0.05). Both EEAA and IEAA were also found to relate to indicators of metabolic syndrome, which appear to mediate their associations with BMI. Metformin-the first-line medication for the treatment of type 2 diabetes-does not delay epigenetic aging in this observational study. Finally, longitudinal data suggests that an increase in BMI is associated with increase in both EEAA and IEAA. Overall, the epigenetic age analysis of blood confirms the conventional wisdom regarding the benefits of eating a high plant diet with lean meats, moderate alcohol consumption, physical activity, and education, as well as the health risks of obesity and metabolic syndrome.
KW - Aging
KW - Alcohol intake
KW - Diet
KW - DNA methylation
KW - Epigenetic clock
KW - Fish intake
KW - Lifestyle
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UR - http://www.scopus.com/inward/citedby.url?scp=85014426881&partnerID=8YFLogxK
U2 - 10.18632/aging.101168
DO - 10.18632/aging.101168
M3 - Article
C2 - 28198702
AN - SCOPUS:85014426881
SN - 1945-4589
VL - 9
SP - 419
EP - 446
JO - Aging
JF - Aging
IS - 2
ER -