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DNA methylome variation in a perinatal nurse-visitation program that reduces child maltreatment: a 27-year follow-up

机译:围产期护士就诊计划中的DNA甲基化组变异减少了对儿童的虐待:27年的随访

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摘要

This study reveals the influence of child maltreatment on DNA methylation across the genome and provides the first evidence that a psychosocial intervention program, the Nurse Family Partnership (NFP), which targets mothers at risk for abusive parenting, associates with variation in the DNA methylome in adult offspring. The 188 participants were born to women randomly assigned to control (n = 99) or nurse-visited intervention groups (n = 89) and provided blood samples and a diagnostic interview at age 27 years. Interindividual variation in the blood DNA methylome was described using principal components (PC) scores derived from principal component analysis and showed that the NFP program (PC10: p = 0.029) and a history of abuseeglect (PC1: p = 0.029, PC2: p = 0.009) significantly associated with DNA methylome variation at 27 years of age independent of gender, ancestry, cellular heterogeneity, and a polygenic risk index for major psychiatric disorders. The magnitude of the association between child maltreatment and DNA methylation was reduced when accounting for lifestyle factors, including smoking. These findings reflect the sustained impact of both childhood adversity as well as intervention programs that target such adversity on the epigenome but highlight the need for prospective longitudinal studies of DNA methylome variation in the context of early intervention programs.
机译:这项研究揭示了虐待儿童对整个基因组DNA甲基化的影响,并提供了第一个证据,即针对有遭受虐待父母风险的母亲的社会心理干预计划“护士家庭伙伴关系”(NFP)与DNA甲基化组的变异相关。成年后代。 188名参与者是由随机分配为对照组(n = 99)或护士干预组(n = 89)的妇女所生,并在27岁时提供了血液样本和诊断性访谈。使用从主成分分析得出的主成分(PC)分数描述了血液DNA甲基化组之间的个体差异,结果表明NFP程序(PC10:p = 0.029)和滥用/忽视的历史(PC1:p = 0.029,PC2: p = 0.009)与27岁时的DNA甲基化组变异显着相关,而与性别,血统,细胞异质性以及主要精神疾病的多基因风险指数无关。考虑到包括吸烟在内的生活方式因素,儿童虐待和DNA甲基化之间的关联程度有所降低。这些发现反映了儿童期逆境以及针对这种逆境的干预计划对表观基因组的持续影响,但强调了在早期干预计划的背景下对DNA甲基化组变异进行前瞻性纵向研究的必要性。

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