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阿拉伯人群代谢综合征的遗传学研究:系统评价与荟萃分析

Genetic Studies of Metabolic Syndrome in Arab Populations: A Systematic Review and Meta-Analysis.

作者信息

Al-Homedi Zahrah, Afify Nariman, Memon Mashal, Alsafar Habiba, Tay Guan, Jelinek Herbert F, Mousa Mira, Abu-Samra Nadia, Osman Wael

机构信息

College of Medicine and Health Sciences, Khalifa University, Abu Dhabi, United Arab Emirates.

Center for Biotechnology, Khalifa University, Abu Dhabi, United Arab Emirates.

出版信息

Front Genet. 2021 Nov 18;12:733746. doi: 10.3389/fgene.2021.733746. eCollection 2021.

Abstract

The metabolic syndrome (MetS) is prevalent in Arabian populations. Several small-scale studies have been performed to investigate the genetic basis of MetS. This systematic review and meta-analysis aimed to examine whether candidate gene polymorphisms are associated with MetS susceptibility among ethnic groups of the Arabian world and to suggest possible directions for future research regarding genetic markers and MetS. A search was conducted for peer-reviewed articles that examined the genetic association of MetS in Arabian populations in the following databases: Medline, Embase, Scopus, Direct Science, Web of Science, ProQuest, and Google Scholar until March 31, 2021. Articles were eligible if they were case-control studies, which investigated MetS as a dichotomous outcome (MetS vs no MetS). To assess the quality of the studies, the Q-Genie tool (Quality of Genetic Association Studies) was used. A non-central chi2 (random-effect) distribution was used to determine the heterogeneity (H) of Q and (Galassi et al., The American journal of medicine, 2006, 119, 812-819) statistics. Our search strategy identified 36 studies that met our inclusion criteria. In most cases, studies were excluded due to a lack of statistical information such as odds ratios, confidence intervals, and -values. According to the Q-Genie tool, 12 studies scored poorly (a score of≤35), 13 studies scored moderately ( >35 and≤45), and 12 studies had good quality ( >45 or higher). The most frequently studied genes were FTO and VDR (both included in four studies). Three SNPs indicated increased risk for MetS after calculating the pooled odds ratios: FTO-rs9939609 (odds ratio 1.49, 95% CI: 0.96-2.32); LEP-rs7799039 (odds ratio 1.85, 95% CI: 1.37-2.5); and SERPINA12-rs2236242 (odds ratio 1.65, 95% CI: 1.21-2.24). Meta-analysis studies showed no significant heterogeneity. There were many sources of heterogeneity in the study settings. Most of the studies had low to moderate quality because of sample size and power issues, not considering all potential sources of bias, and not providing details about genotyping methods and results. As most studies were small-scale, aimed to replicate findings from other populations, we did not find any unique genetic association between MetS and Arabian populations.

摘要

代谢综合征(MetS)在阿拉伯人群中普遍存在。已经开展了多项小规模研究来探究MetS的遗传基础。本系统评价和荟萃分析旨在检验候选基因多态性与阿拉伯世界各民族MetS易感性之间是否存在关联,并为未来关于遗传标记和MetS的研究提出可能的方向。在以下数据库中搜索了对阿拉伯人群中MetS遗传关联进行研究的同行评审文章:医学期刊数据库(Medline)、荷兰医学文摘数据库(Embase)、Scopus数据库、Direct Science数据库、科学引文索引数据库(Web of Science)、ProQuest数据库和谷歌学术搜索数据库,检索截至2021年3月31日的文献。若文章为病例对照研究且将MetS作为二分结局(存在MetS与不存在MetS)进行调查,则符合纳入标准。使用Q-Genie工具(遗传关联研究质量工具)评估研究质量。采用非中心卡方(随机效应)分布来确定Q统计量和(加拉西等人,《美国医学杂志》,2006年,第119卷,812 - 819页)统计量的异质性(H)。我们的检索策略共识别出36项符合纳入标准的研究。在大多数情况下,由于缺乏诸如比值比、置信区间和P值等统计信息,这些研究被排除。根据Q-Genie工具,12项研究得分较低(得分≤35),13项研究得分中等(得分>35且≤45),12项研究质量良好(得分>45或更高)。研究最频繁的基因是FTO和VDR(均有四项研究涉及)。在计算合并比值比后,三个单核苷酸多态性(SNP)表明MetS风险增加:FTO-rs9939609(比值比1.49,95%置信区间:0.96 - 2.32);LEP-rs7799039(比值比1.85,95%置信区间:1.37 - 2.5);以及SERPINA12-rs2236242(比值比1.65,95%置信区间:1.21 - 2.24)。荟萃分析研究显示无显著异质性。研究背景中存在许多异质性来源。由于样本量和检验效能问题、未考虑所有潜在偏倚来源以及未提供基因分型方法和结果的详细信息,大多数研究质量低至中等。由于大多数研究规模较小,旨在重复其他人群的研究结果,我们未发现MetS与阿拉伯人群之间存在任何独特的遗传关联。

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