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NFATC2IP 基因座的遗传、表观遗传和转录变异与饮食干预减肥的反应有关:POUNDS LOST 试验。

Genetic, epigenetic and transcriptional variations at NFATC2IP locus with weight loss in response to diet interventions: The POUNDS Lost Trial.

机构信息

Department of Epidemiology, School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana.

Department of Pediatrics, Children's Hospital New Orleans, New Orleans, Louisiana.

出版信息

Diabetes Obes Metab. 2018 Sep;20(9):2298-2303. doi: 10.1111/dom.13333. Epub 2018 May 24.

DOI:10.1111/dom.13333
PMID:29693310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6105429/
Abstract

DNA Methylation of NFATC2IP was recently identified as being causally related to body mass index. The present study aimed to examine the roles of the genetic variation, methylation and gene expression at this locus in adiposity changes in a 2-year weight-loss trial. Participants (n = 692) were genotyped and randomly assigned to 1 of the 4 reduced-calorie diets, DNA methylation was derived from stored blood samples at baseline (n = 48), and adipose tissue gene expression was measured in 96 volunteers. We found significant interactions of fat intake with the genetic (rs11150675) and transcriptional (ILMN_1725441) variations at the NFATC2IP locus on 2-year weight change (P < .01). Similarly, cis-DNA methylation at cg26663590 of the NFATC2IP locus showed an opposite impact on weight-loss in response to high-fat vs low-fat diet (effect size, 4.62 vs -1.24 kg). Additionally, baseline methylation at cg26663590 causally mediated 52.8% of the effect of rs11150675 on 2-year weight-loss in the high-fat diet group (P = .01), whereas no such mediation was observed in the low-fat diet group. Our findings suggest potentially causal effects of genetic, epigenetic and transcriptional variations at the NFATC2IP locus on adiposity changes in response to dietary fat intake.

摘要

NFATC2IP 的 DNA 甲基化最近被确定与体重指数有关。本研究旨在探讨该基因座的遗传变异、甲基化和基因表达在为期 2 年的减肥试验中体脂变化中的作用。参与者(n = 692)进行了基因分型,并随机分配到 4 种低热量饮食中的 1 种,基线时(n = 48)从储存的血液样本中提取 DNA 甲基化,96 名志愿者测量了脂肪组织基因表达。我们发现,脂肪摄入量与 NFATC2IP 基因座上的遗传(rs11150675)和转录(ILMN_1725441)变异在 2 年内体重变化上存在显著交互作用(P <.01)。同样,NFATC2IP 基因座上的 cis-DNA 甲基化在高、低脂饮食下对减肥的影响相反(效应大小,4.62 与-1.24 kg)。此外,基线时 cg26663590 处的 NFATC2IP 甲基化在高脂肪饮食组中对 rs11150675 对 2 年体重减轻的影响有 52.8%的因果中介作用(P =.01),而在低脂饮食组中则没有观察到这种中介作用。我们的研究结果表明,NFATC2IP 基因座上的遗传、表观遗传和转录变异对饮食脂肪摄入引起的体脂变化可能有因果影响。

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