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FTO基因变异rs1421085在与肥胖关系中的作用:一项系统评价和荟萃分析。

The role of FTO variant rs1421085 in the relationship with obesity: a systematic review and meta-analysis.

作者信息

Najd-Hassan-Bonab Leila, Safarpour Mahdi, Moazzam-Jazi Maryam, Azizi Fereidoun, Daneshpour Maryam S

机构信息

Cellular and Molecular Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, No 24, Parvaneh St, Yemen St, Chamran Exp, PO Box 1985717413, Tehran, Iran.

Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Eat Weight Disord. 2022 Dec;27(8):3053-3062. doi: 10.1007/s40519-022-01509-0. Epub 2022 Nov 25.

Abstract

PURPOSE

Fat mass and obesity-associated (FTO) is considered the first locus associated with adiposity, a concerning health problem worldwide. Many studies have evaluated the relationship between the FTO variants and obesity susceptibility. While the strong association of FTO rs1421085 with the risk of obesity across populations was reported in different studies, some researchers found a lack of association of this variant with adiposity. This systematic review and meta-analysis aimed to assess the association between obesity and rs1421085 polymorphism.

METHODS

We systematically searched PubMed, Scopus, and Google Scholar up to June 2022 to find pertinent studies. To further assess this issue, we surveyed the probable association of rs1421085 with obesity development among Iranian adults using the logistic regression analysis, and the obtained results were used for doing meta-analysis. After selection, nine eligible studies were included in the meta-analysis through the random- and fixed-effect models to determine the combined odds ratios (OR) and 95% confidence intervals (CI).

RESULTS

According to our meta-analysis conducted on 5169 obese and 7772 non-obese individuals using different genetic models, including recessive, dominant, over-dominant, and additive, rs1421085 could positively increase the risk of obesity under all tested genetic models. Also, we detected a high to moderate level of heterogeneity among different studies under various genetic models.

CONCLUSION

This meta-analysis further verified the positive association of FTO rs1421085 with the risk of developing obesity.

STUDY REGISTRATION

This study is registered as PROSPERO CRD42021220092.

LEVEL OF EVIDENCE

Level I, systematic reviews and meta-analyses.

摘要

目的

脂肪量和肥胖相关基因(FTO)被认为是首个与肥胖相关的基因位点,肥胖是一个全球范围内令人担忧的健康问题。许多研究评估了FTO基因变异与肥胖易感性之间的关系。虽然不同研究报告了FTO rs1421085与人群肥胖风险之间存在强关联,但一些研究人员发现该变异与肥胖并无关联。本系统评价和荟萃分析旨在评估肥胖与rs1421085多态性之间的关联。

方法

我们系统检索了截至2022年6月的PubMed、Scopus和谷歌学术,以查找相关研究。为进一步评估该问题,我们使用逻辑回归分析调查了伊朗成年人中rs1421085与肥胖发生的可能关联,并将所得结果用于荟萃分析。筛选后,通过随机效应模型和固定效应模型,将9项符合条件的研究纳入荟萃分析,以确定合并比值比(OR)和95%置信区间(CI)。

结果

根据我们对5169名肥胖个体和7772名非肥胖个体使用隐性、显性、超显性和加性等不同遗传模型进行的荟萃分析,rs1421085在所有测试的遗传模型下均能正向增加肥胖风险。此外,我们在不同遗传模型下的不同研究中检测到高到中度的异质性。

结论

该荟萃分析进一步证实了FTO rs1421085与肥胖发生风险之间存在正相关。

研究注册

本研究已注册为PROSPERO CRD42021220092。

证据水平

I级,系统评价和荟萃分析。

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