Low birthweight is associated with epigenetic age acceleration in the first 3 years of life

被引:4
作者
Quinn, Edward B. [1 ,2 ]
Hsiao, Chu J. [1 ,2 ,3 ]
Maisha, Felicien M. [1 ,2 ,4 ,5 ]
Mulligan, Connie J. [1 ,2 ,6 ]
机构
[1] Univ Florida, Dept Anthropol, Gainesville, FL 32608 USA
[2] Univ Florida, Genet Inst, Gainesville, FL 32608 USA
[3] Univ Florida, Coll Med, Gainesville, FL 32608 USA
[4] HEAL Africa Hosp, Goma, DEM REP CONGO
[5] Maisha Inst, Goma, DEM REP CONGO
[6] Univ Florida, Dept Anthropol, 2033 Mowry Rd,POB 103610, Gainesville, FL 32610 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
aging; birthweight; developmental origins of health and disease; DNA methylation; early life adversity; epigenetic aging; METHYLATION; STRESS; DEPRESSION; NEWBORNS; VIOLENCE; ORIGINS;
D O I
10.1093/emph/eoad019
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lay Summary Low birthweight is associated with poor adult health outcomes, but the mechanism is unclear. We tested for a relationship between low birthweight and accelerated aging based on DNA methylation. Low birthweight predicted accelerated aging among infants, suggesting potential connections between birthweight, accelerated aging and adult health. Background and objectives The Developmental Origins of Health and Disease hypothesis posits that early life adversity is associated with poor adult health outcomes. Epidemiological evidence has supported this framework by linking low birthweight with adult health and mortality, but the mechanisms remain unclear. Accelerated epigenetic aging may be a pathway to connect early life experiences with adult health outcomes, based on associations of accelerated epigenetic aging with increased morbidity and mortality. Methodology Sixty-seven mother-infant dyads were recruited in the eastern Democratic Republic of Congo. Birthweight data were collected at birth, and blood samples were collected at birth and follow-up visits up to age 3. DNA methylation data were generated with the Illumina MethylationEPIC array and used to estimate epigenetic age. A multilevel model was used to test for associations between birthweight and epigenetic age acceleration. Results Chronological age was highly correlated with epigenetic age from birth to age 3 (r = 0.95, p < 2.2 x 10(-16)). Variation in epigenetic age acceleration increased over time. Birthweight, dichotomized around 2500 g, predicted epigenetic age acceleration over the first 3 years of life (b = -0.39, p = 0.005). Conclusions and implications Our longitudinal analysis provides the first evidence for accelerated epigenetic aging that emerges between birth and age 3 and associates with low birthweight. These results suggest that early life experiences, such as low birthweight, may shape the trajectory of epigenetic aging in early childhood. Furthermore, accelerated epigenetic aging may be a pathway that links low birthweight and poor adult health outcomes.
引用
收藏
页码:251 / 261
页数:11
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