DNA methylation as a possible mechanism linking childhood adversity and health: results from a 2-sample mendelian randomization study

被引:6
作者
Schuurmans, Isabel K. [1 ,2 ]
Dunn, Erin C. [1 ,3 ,4 ]
Lussier, Alexandre A. [1 ,3 ,4 ]
机构
[1] Massachusetts Gen Hosp, Ctr Genom Med, Psychiat & Neurodev Genet Unit, Boston, MA 02114 USA
[2] Erasmus MC, Dept Epidemiol, Univ Med Ctr Rotterdam, NL-3000 CA Rotterdam, Netherlands
[3] Harvard Med Sch, Dept Psychiat, Boston, MA 02215 USA
[4] Broad Inst Harvard & MIT, Stanley Ctr Psychiat Res, Cambridge, MA 02142 USA
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
childhood adversity; epigenetics; DNA methylation; mental health; physical health; mendelian randomization; GENOME-WIDE ASSOCIATION; CAUSAL ROLE; DISEASE; DETERMINANTS; METAANALYSIS; EXPERIENCES; DISORDERS; PATTERNS; SMOKING; STRESS;
D O I
10.1093/aje/kwae072
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Childhood adversity is an important risk factor for adverse health across the life course. Epigenetic modifications, such as DNA methylation (DNAm), are a hypothesized mechanism linking adversity to disease susceptibility. Yet, few studies have determined whether adversity-related DNAm alterations are causally related to future health outcomes or if their developmental timing plays a role in these relationships. Here, we used 2-sample mendelian randomization to obtain stronger causal inferences about the association between adversity-associated DNAm loci across development (ie, birth, childhood, adolescence, and young adulthood) and 24 mental, physical, and behavioral health outcomes. We identified particularly strong associations between adversity-associated DNAm and attention-deficit/hyperactivity disorder, depression, obsessive-compulsive disorder, suicide attempts, asthma, coronary artery disease, and chronic kidney disease. More of these associations were identified for birth and childhood DNAm, whereas adolescent and young adulthood DNAm were more closely linked to mental health. Childhood DNAm loci also had primarily risk-suppressing relationships with health outcomes, suggesting that DNAm might reflect compensatory or buffering mechanisms against childhood adversity rather than acting solely as an indicator of disease risk. Together, our results suggest adversity-related DNAm alterations are linked to both physical and mental health outcomes, with particularly strong impacts of DNAm differences emerging earlier in development.
引用
收藏
页码:1541 / 1552
页数:12
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