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昼夜节律钟基因多态性与代谢综合征之间的关联:一项系统评价和荟萃分析。

The Association between Circadian Clock Gene Polymorphisms and Metabolic Syndrome: A Systematic Review and Meta-Analysis.

作者信息

Škrlec Ivana, Talapko Jasminka, Džijan Snježana, Cesar Vera, Lazić Nikolina, Lepeduš Hrvoje

机构信息

Faculty of Dental Medicine and Health Osijek, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia.

Genos Ltd., DNA Laboratory, 10000 Zagreb, Croatia.

出版信息

Biology (Basel). 2021 Dec 24;11(1):20. doi: 10.3390/biology11010020.

Abstract

Metabolic syndrome (MetS) is a combination of cardiovascular risk factors associated with type 2 diabetes, obesity, and cardiovascular diseases. The circadian clock gene polymorphisms are very likely to participate in metabolic syndrome genesis and development. However, research findings of the association between circadian rhythm gene polymorphisms and MetS and its comorbidities are not consistent. In this study, a review of the association of circadian clock gene polymorphisms with overall MetS risk was performed. In addition, a meta-analysis was performed to clarify the association between circadian clock gene polymorphisms and MetS susceptibility based on available data. The PubMed and Scopus databases were searched for studies reporting the association between circadian rhythm gene polymorphisms (ARNTL, BMAL1, CLOCK, CRY, PER, NPAS2, REV-ERBα, REV-ERBβ, and RORα) and MetS, and its comorbidities diabetes, obesity, and hypertension. Thirteen independent studies were analyzed with 17,381 subjects in total. The results revealed that the BMAL1 rs7950226 polymorphism was associated with an increased risk of MetS in the overall population. In contrast, the CLOCK rs1801260 and rs6850524 polymorphisms were not associated with MetS. This study suggests that some circadian rhythm gene polymorphisms might be associated with MetS in different populations and potentially used as predictive biomarkers for MetS.

摘要

代谢综合征(MetS)是与2型糖尿病、肥胖症和心血管疾病相关的心血管危险因素的组合。昼夜节律时钟基因多态性很可能参与代谢综合征的发生和发展。然而,关于昼夜节律基因多态性与代谢综合征及其合并症之间关联的研究结果并不一致。在本研究中,对昼夜节律时钟基因多态性与总体代谢综合征风险的关联进行了综述。此外,基于现有数据进行了荟萃分析,以阐明昼夜节律时钟基因多态性与代谢综合征易感性之间的关联。在PubMed和Scopus数据库中检索了报告昼夜节律基因多态性(ARNTL、BMAL1、CLOCK、CRY、PER、NPAS2、REV-ERBα、REV-ERBβ和RORα)与代谢综合征及其合并症糖尿病、肥胖症和高血压之间关联的研究。对13项独立研究进行了分析,共有17381名受试者。结果显示,BMAL1 rs7950226多态性与总体人群中代谢综合征风险增加相关。相比之下,CLOCK rs1801260和rs6850524多态性与代谢综合征无关。本研究表明,一些昼夜节律基因多态性可能在不同人群中与代谢综合征相关,并有可能用作代谢综合征的预测生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a49/8773381/789729aaf563/biology-11-00020-g001.jpg

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