Aging and epigenetics Longitudinal changes in gene-specific DNA methylation

被引:77
|
作者
Madrigano, Jaime [1 ,2 ,3 ]
Baccarelli, Andrea [3 ]
Mittleman, Murray A. [4 ,5 ]
Sparrow, David [6 ,7 ,8 ]
Vokonas, Pantel S. [6 ,7 ]
Tarantini, Letizia [9 ,10 ]
Schwartz, Joel [3 ,4 ]
机构
[1] Columbia Univ, Earth Inst, New York, NY 10027 USA
[2] Columbia Univ, Mailman Sch Publ Hlth, New York, NY USA
[3] Harvard Univ, Sch Publ Hlth, Dept Environm Hlth, Boston, MA 02115 USA
[4] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[5] Beth Israel Deaconess Med Ctr, Cardiovasc Epidemiol Res Unit, Boston, MA 02215 USA
[6] Boston Univ, Sch Med, VA Boston Healthcare Syst, VA Normat Aging Study, Boston, MA 02118 USA
[7] Boston Univ, Sch Med, Dept Med, Boston, MA 02118 USA
[8] Harvard Univ, Brigham & Womens Hosp, Sch Med, Channing Lab, Boston, MA 02115 USA
[9] Univ Milan, Ctr Mol & Genet Epidemiol, IRCCS Ca Granda Maggiore Policlin Hosp Fdn, Milan, Italy
[10] Univ Milan, Dept Environm & Occupat Hlth, Milan, Italy
基金
美国国家卫生研究院;
关键词
aging; DNA methylation; epigenesis; genetic; PROMOTER METHYLATION; AGE; ATHEROSCLEROSIS; NEOPLASIA;
D O I
10.4161/epi.7.1.18749
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA methylation has been associated with age-related disease. Intra-individual changes in gene-specific DNA methylation over time in a community-based cohort has not been well described. We estimated the change in DNA methylation due to aging for nine genes in an elderly, community-dwelling cohort of men. Seven hundred and eighty four men from the Veterans Administration Normative Aging Study who were living in metropolitan Boston from 19992009 donated a blood sample for DNA methylation analysis at clinical examinations repeated at approximately 3-5 year intervals. We used mixed effects regression models. Aging was significantly associated with decreased methylation of GCR, iNOS and TLR2 and with increased methylation of IFN gamma, F3, CRAT and OGG. Obstructive pulmonary disease at baseline modified the effect of aging on methylation of IFN gamma (interaction p = 0.04). For participants who had obstructive pulmonary disease at their baseline visit, the rate of change of methylation of IFN gamma was -0.05% 5-methyl-cytosine (5-mC) per year (95% CI: -0.22, 0.13), but was 0.14% 5-mC per year (95% CI: 0.05, 0.24) for those without this condition. Models with random slopes indicated significant heterogeneity in the effect of aging on methylation of GCR, iNOS and OGG. These findings suggest that DNA methylation may reflect differential biological aging.
引用
收藏
页码:63 / 70
页数:8
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