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
N1 - Funding Information:
We would like to acknowledge The WHI Investigators listed below: Program Office: (National Heart, Lung, and Blood Institute, Bethesda, Maryland) Jacques Rossouw, Shari Ludlam, Dale Burwen, Joan McGowan, Leslie Ford, and Nancy Geller. Clinical Coordinating Center: (Fred Hutchinson Cancer Research Center, Seattle, WA) Garnet Anderson, Ross Prentice, Andrea LaCroix, and Charles Kooperberg. Investigators and Academic Centers: (Brigham and Women's Hospital, Harvard Medical School, Boston, MA) JoAnn E. Manson; (MedStar Health Research Institute/Howard University, Washington, DC) Barbara V. Howard; (Stanford Prevention Research Center, Stanford, CA). Marcia L. Stefanick; (The Ohio State University, Columbus, OH) Rebecca Jackson; (University of Arizona, Tucson/Phoenix, AZ) Cynthia A. Thomson; (University at Buffalo, Buffalo, NY) Jean Wactawski-Wende; (University of Florida, Gainesville/Jacksonville, FL) Marian Limacher; (University of Iowa, Iowa City/Davenport, IA) Robert Wallace; (University of Pittsburgh, Pittsburgh, PA) Lewis Kuller; (Wake Forest University School of Medicine, Winston-Salem, NC) Sally Shumaker. Women's Health Initiative Memory Study: (Wake Forest University School of Medicine, Winston-Salem, NC) Sally Shumaker. This WHI study was supported by National Institutes of Health NIH/NHLBI 60442456 BAA23 (Assimes, Absher, Horvath) and the National Institute of Environmental Health Sciences R01ES020836 WHIEMPC (Whitsel, Baccarelli, Hou), R01ES021733 (Baccarelli), and R01ES025225 (Baccarelli). The WHI program is funded by the National Heart, Lung, and Blood Institute, National Institutes of Health, U.S. Department of Health and Human Services through contracts HHSN268201100046C, HHSN268201100001C, HHSN268201100002C, HHSN268201100003C, HHSN268201100004C, and HHSN271201100004C. The authors thank the WHI investigators and staff for their dedication, and the study participants for making the program possible. A full listing of WHI investigators can be found at: www.whi.org/researchers/ Documents%20%20Write%20a%20Paper/WHI%20Inve stigator%20Short%20List.pdf. Additional support came from NIH/NIA 5R01AG042511-02 (Horvath), NIH/NIA U34AG051425-01 (Horvath), NIH/NINDS T32NS048004 (Levine), and the Burroughs Wellcome Fund Inter-school Training Program in Chronic Diseases (BWF-CHIP, Quach). The funding bodies played no role in the design, the collection, analysis, or interpretation of the data. The InCHIANTI study baseline (1998-2000) was supported as a "targeted project" (ICS110.1/RF97.71) by the Italian Ministry of Health and in part by the U.S. National Institute on Aging (Contracts: 263 MD 9164 and 263 MD 821336).
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 - DNA methylation
KW - Diet
KW - Epigenetic clock
KW - Fish intake
KW - Lifestyle
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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 -