Reproduction, DNA methylation and biological age

被引:33
作者
Kresovich, Acob K. [1 ]
Harmon, Quaker E. [1 ]
Xu, Zongli [1 ]
Nichols, Hazel B. [2 ]
Sandler, Dale R. [1 ]
Taylor, Jack A. [1 ,3 ]
机构
[1] NIEHS, Epidemiol Branch, NIH, Res Triangle Pk, NC 27709 USA
[2] Univ North Carolina Chapel Hill, Dept Epidemiol, Gillings Sch Global Publ Hlth, Chapel Hill, NC 27599 USA
[3] NIEHS, Epigenet & Stem Cell Biol Lab, NIH, Res Triangle Pk, NC 27709 USA
关键词
parity; pregnancy complications; epigenetic clock; DNA methylation; biological age; HYPERTENSIVE DISEASE; ALL-CAUSE; PREGNANCY; MORTALITY; OBESITY; PARITY;
D O I
10.1093/humrep/dez149
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
STUDY QUESTION: Are reproductive characteristics associated with genome-wide DNA methylation and epigenetic age? SUMMARY ANSWER: Our data suggest that increasing parity is associated with differences in blood DNA methylation and small increases in epigenetic age. WHAT IS KNOWN ALREADY: A study of 397 young Filipino women (ages 20-22) observed increasing epigenetic age with an increasing number of pregnancies. STUDY DESIGN, SIZE, DURATION: We used data from 2356 non-Hispanic white women (ages 35-74) enrolled in the Sister Study cohort. PARTICIPANTS/MATERIALS, SETTING, METHODS: Data on reproductive history were ascertained via questionnaire. Of the 2356 women, 1897 (81%) reported at least one live birth. Among parous women, 487 (26%) women reported ever experiencing a pregnancy complication. Three epigenetic clocks (i.e. Hannum, Horvath and Levine) and genome-wide methylation were measured in DNA from whole blood using Illumina's HumanMethylation450 BeadChip. We estimated association fl-values and 95% Cis using linear regression. MAIN RESULTS AND THE ROLE OF CHANCE: All three epigenetic docks showed weak associations between number of births and epigenetic age (per live birth; Hannum: beta = 0.16, 95% CI = 0.02, 0.29, P = 0.03; Horvath: beta = 0.12, 95% CI = -0.04, 0.27, P = 0.14; Levine:beta = 0.27, 95% CI = 0.08, 0.45, P = 0.01); however, additional adjustment for current BMI attenuated the associations. Among parous women, a history of abnormal glucose tolerance during pregnancy was associated with increased epigenetic age by the Hannum clock (beta = 0.96; 95% CI = 0.10, 1.81; P = 0.03) and Levine clocks (beta = 1.69; 95% CI = 0.54, 2.84; P < 0.01). In epigenome-wide analysis, increasing parity was associated with methylation differences at 17 CpG sites (Bonferroni corrected P <= 1.0 x 10(-7)). LIMITATIONS, REASONS FOR CAUTION: We relied on retrospective recall to ascertain reproductive history and pregnancy complications. WIDER IMPLICATIONS OF THE FINDINGS: Our findings suggest that parity is associated with small increases in epigenetic age and with DNA methylation at multiple sites in the genome.
引用
收藏
页码:1965 / 1973
页数:9
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