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