» Articles » PMID: 32695830

Associations of Polymorphisms with the Risk of Type 2 Diabetes Mellitus: An Updated Meta-Analysis with Trial Sequential Analysis

Overview
Journal J Diabetes Res
Publisher Wiley
Specialty Endocrinology
Date 2020 Jul 23
PMID 32695830
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Previous studies have examined the role of the KQT-like subfamily Q member1 () gene polymorphisms on the risk of type 2 diabetes mellitus (T2DM), but the findings are inconclusive.

Objective: To examine the association between the gene polymorphisms and the risk of T2DM using an updated meta-analysis with an almost tripled number of studies.

Methods: Five electronic databases, such as PubMed and Embase, were searched thoroughly for relevant studies on the associations between seven most studied gene polymorphisms, including rs2237892, rs2237897, rs2237895, rs2283228, rs231362, rs151290, and rs2074196, and T2DM risk up to September 14, 2019. The summary odds ratios (ORs) with their 95% confidence intervals (CIs) were applied to assess the strength of associations in the random-effects models. We used the trial sequential analysis (TSA) to measure the robustness of the evidence.

Results: 49 publications including 55 case-control studies (68,378 cases and 66,673 controls) were finally enrolled. In overall analyses, generally, increased T2DM risk was detected for rs2237892, rs2237895, rs2283228, rs151290, and rs2074196, but not for rs231362 under all genetic models. The ORs and 95% CIs for allelic comparison were 1.23 (1.14-1.33) for rs2237892, 1.21 (1.16-1.27) for rs2237895, 1.27 (1.11-1.46) for rs2237897, 1.25 (1.09-1.42) for rs2283228, 1.14 (1.03-1.27) for rs151290, 1.31 (1.23-1.39) for rs2074196, and 1.16 (0.83, 1.61) for rs231362. Stratified analyses showed that associations for rs2237892, rs2237895, rs2283228, and rs151290 were more evident among Asians than Caucasians. TSA demonstrated that the evidence was sufficient for all polymorphisms in this study. The genotypes of the three SNPs (rs2237892, rs2283228, and rs231362) were significantly correlated with altered KCNQ1 gene expression.

Conclusion: This meta-analysis suggested that gene polymorphisms (rs2237892, rs2283228, rs2237895, rs151290, and rs2074196) might be the susceptible factors for T2DM, especially among Asian population.

Citing Articles

Genetic and epigenetic alterations associated with gestational diabetes mellitus and adverse neonatal outcomes.

Shamsad A, Gautam T, Singh R, Banerjee M World J Clin Pediatr. 2025; 14(1):99231.

PMID: 40059904 PMC: 11686586. DOI: 10.5409/wjcp.v14.i1.99231.


Suppression of P2X7R by Local Treatment Alleviates Acute Gouty Inflammation.

Zhao Y, Li Z, Chen Y, Li Y, Lu J J Inflamm Res. 2023; 16:3581-3591.

PMID: 37636273 PMC: 10460186. DOI: 10.2147/JIR.S421548.


Bulk and single-cell transcriptome analyses of islet tissue unravel gene signatures associated with pyroptosis and immune infiltration in type 2 diabetes.

Song Y, He C, Jiang Y, Yang M, Xu Z, Yuan L Front Endocrinol (Lausanne). 2023; 14:1132194.

PMID: 36967805 PMC: 10034023. DOI: 10.3389/fendo.2023.1132194.


Genetic Risk Scores for the Determination of Type 2 Diabetes Mellitus (T2DM) in North India.

Shitomi-Jones L, Akam L, Hunter D, Singh P, Mastana S Int J Environ Res Public Health. 2023; 20(4).

PMID: 36834424 PMC: 9959290. DOI: 10.3390/ijerph20043729.


and Gene Polymorphisms and Placental Expression in Women with Gestational Diabetes Mellitus.

Majcher S, Ustianowski P, Malinowski D, Czerewaty M, Tarnowski M, Safranow K Genes (Basel). 2022; 13(8).

PMID: 35893051 PMC: 9331982. DOI: 10.3390/genes13081315.


References
1.
Mussig K, Staiger H, Machicao F, Kirchhoff K, Guthoff M, Schafer S . Association of type 2 diabetes candidate polymorphisms in KCNQ1 with incretin and insulin secretion. Diabetes. 2009; 58(7):1715-20. PMC: 2699873. DOI: 10.2337/db08-1589. View

2.
Saif-Ali R, Muniandy S, Al-Hamodi Z, Lee C, Ahmed K, Al-Mekhlafi A . KCNQ1 variants associate with type 2 diabetes in Malaysian Malay subjects. Ann Acad Med Singap. 2011; 40(11):488-92. View

3.
Lee M, Ravenel J, Hu R, Lustig L, Tomaselli G, Berger R . Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice. J Clin Invest. 2000; 106(12):1447-55. PMC: 387258. DOI: 10.1172/JCI10897. View

4.
Liu L, Wang F, Lu H, Ren X, Zou J . Chromanol 293B, an inhibitor of KCNQ1 channels, enhances glucose-stimulated insulin secretion and increases glucagon-like peptide-1 level in mice. Islets. 2014; 6(4):e962386. PMC: 4588556. DOI: 10.4161/19382014.2014.962386. View

5.
Lin Y, Qian Y, Dong M, Lu F, Shen C, Jin G . [Association of polymorphisms of potassium voltage-gated channel, KQT-like subfamily, member 1 and type 2 diabetes in Jiangsu province, China]. Zhonghua Yu Fang Yi Xue Za Zhi. 2013; 47(6):538-41. View