Horm Metab Res 2021; 53(01): 49-55
DOI: 10.1055/a-1229-1604
Endocrine Care

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

Na Liu
1   Department of Neurology, Xuzhou Children’s Hospital, Xuzhou Medical University, Xuzhou, China
,
Yan Sang
1   Department of Neurology, Xuzhou Children’s Hospital, Xuzhou Medical University, Xuzhou, China
,
Shengzhi Chen
1   Department of Neurology, Xuzhou Children’s Hospital, Xuzhou Medical University, Xuzhou, China
,
Xiaoming Liu
1   Department of Neurology, Xuzhou Children’s Hospital, Xuzhou Medical University, Xuzhou, China
› Author Affiliations

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.

Supplementary Material



Publication History

Received: 12 May 2020

Accepted after revision: 20 July 2020

Article published online:
04 September 2020

© 2020. Thieme. All rights reserved.

Georg Thieme Verlag KG
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