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载脂蛋白脂蛋白脂酶 S447X 及 HindIII 多态性与 2 型糖尿病风险的相关性:荟萃分析。

Associations of the LPL S447X and Hind III Polymorphism with Type 2 Diabetes Mellitus Risk: A Meta-Analysis.

机构信息

Department of Neurology, Xuzhou Children's Hospital, Xuzhou Medical University, Xuzhou, China.

出版信息

Horm Metab Res. 2021 Jan;53(1):49-55. doi: 10.1055/a-1229-1604. Epub 2020 Sep 4.

Abstract

The present study was aimed to evaluate the association of lipoprotein lipase (LPL) gene (S447X and Hind III) polymorphisms and T2DM. Relevant studies were identified through systematic search PubMed, Cochrane Library, Embase, Wanfang, CNKI databases. A total of 22 studies (8 studies for LPL S447X and 14 studies for Hind III) were included. The results showed that the LPL S447X polymorphism was associated with the low risk of T2DM under dominant and allelic genetic models. Subgroup analysis by ethnicity showed that the LPL S447X polymorphism was associated with a decreased risk of T2DM in the Asian population (under dominant, heterozygous and allelic genetic models). In addition, we found that X allele carriers of S447X polymorphism is associated with low levels of TC, TG, and LDL. In subgroup analysis, Hind III polymorphism was associated with low risk of T2DM in Asian populations (under dominant, heterozygote, allele genetic models). Moreover, the carriers of H allele of Hind III have lower levels of TG, and higher levels of HDL-C. This meta-analysis demonstrated that 447X carriers and H allele in LPL gene associated with low risk of T2DM, which may due to in part to the change of serum level of TC, TG, LDL, and HDL.

摘要

本研究旨在评估脂蛋白脂肪酶(LPL)基因(S447X 和 Hind III)多态性与 T2DM 的关系。通过系统检索 PubMed、Cochrane Library、Embase、万方、CNKI 数据库,确定了相关研究。共纳入 22 项研究(8 项研究用于 LPL S447X,14 项研究用于 Hind III)。结果表明,LPL S447X 多态性在显性和等位基因遗传模型下与 T2DM 的低风险相关。按种族进行的亚组分析表明,LPL S447X 多态性与亚洲人群 T2DM 的低风险相关(在显性、杂合子和等位基因遗传模型下)。此外,我们发现 S447X 多态性的 X 等位基因携带者与 TC、TG 和 LDL 水平降低相关。在亚组分析中,Hind III 多态性与亚洲人群 T2DM 的低风险相关(在显性、杂合子、等位基因遗传模型下)。此外,Hind III 的 H 等位基因携带者的 TG 水平较低,HDL-C 水平较高。这项荟萃分析表明,LPL 基因中的 447X 携带者和 H 等位基因与 T2DM 的低风险相关,这可能部分归因于 TC、TG、LDL 和 HDL 血清水平的变化。

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