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探讨肥胖与 DNA 甲基化之间的关联:系统评价和荟萃分析。

Examining the association between adiposity and DNA methylation: A systematic review and meta-analysis.

机构信息

Nutrition and Health Sciences Program, Laney Graduate School, Emory University, Atlanta, Georgia, USA.

Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, Georgia, USA.

出版信息

Obes Rev. 2021 Oct;22(10):e13319. doi: 10.1111/obr.13319. Epub 2021 Jul 18.

Abstract

Obesity is associated with widespread differential DNA methylation (DNAm) patterns, though there have been limited overlap in the obesity-associated cytosine-guanine nucleotide pair (CpG) sites that have been identified in the literature. We systematically searched four databases for studies published until January 2020. Eligible studies included cross-sectional, longitudinal, or intervention studies examining adiposity and genome-wide DNAm in non-pregnant adults aged 18-75 in all tissue types. Study design and results were extracted in the descriptive review. Blood-based DNAm results in body mass index (BMI) and waist circumference (WC) were meta-analyzed using weighted sum of Z-score meta-analysis. Of the 10,548 studies identified, 46 studies were included in the systematic review with 18 and nine studies included in the meta-analysis of BMI and WC, respectively. In the blood, 77 and four CpG sites were significant in three or more studies of BMI and WC, respectively. Using a genome-wide threshold for significance, 52 blood-based CpG sites were significantly associated with BMI. These sites have previously been associated with many obesity-related diseases including type 2 diabetes, cardiovascular disease, Crohn's disease, and depression. Our study shows that DNAm at 52 CpG sites represent potential mediators of obesity-associated chronic diseases and may be novel intervention or therapeutic targets to protect against obesity-associated chronic diseases.

摘要

肥胖与广泛的差异 DNA 甲基化(DNAm)模式有关,但在文献中确定的与肥胖相关的胞嘧啶-鸟嘌呤核苷酸对(CpG)位点之间存在有限的重叠。我们系统地在四个数据库中搜索了截至 2020 年 1 月发表的研究。合格的研究包括横断面、纵向或干预研究,检查非孕妇 18-75 岁所有组织类型的肥胖和全基因组 DNAm。在描述性综述中提取了研究设计和结果。使用加权 Z 分数总和荟萃分析对血液中基于 DNAm 的体重指数(BMI)和腰围(WC)结果进行荟萃分析。在鉴定的 10548 项研究中,有 46 项研究被纳入系统评价,其中 18 项和 9 项研究分别被纳入 BMI 和 WC 的荟萃分析。在血液中,77 个和 4 个 CpG 位点在 BMI 和 WC 的三个或更多研究中具有统计学意义。使用全基因组显著性阈值,有 52 个基于血液的 CpG 位点与 BMI 显著相关。这些位点先前与许多肥胖相关疾病有关,包括 2 型糖尿病、心血管疾病、克罗恩病和抑郁症。我们的研究表明,52 个 CpG 位点的 DNAm 代表肥胖相关慢性疾病的潜在介质,并且可能是新的干预或治疗靶点,以预防肥胖相关的慢性疾病。

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