Published online Mar 15, 2024. doi: 10.4239/wjd.v15.i3.552
Peer-review started: September 25, 2023
First decision: December 6, 2023
Revised: December 13, 2023
Accepted: February 2, 2024
Article in press: February 2, 2024
Published online: March 15, 2024
Processing time: 172 Days and 2 Hours
The association of single nucleotide polymorphism of KCNQ1 gene rs2237895 with type 2 diabetes mellitus (T2DM) is currently controversial. It is unknown whether this association can be gene realized across different populations.
To determine the association of KCNQ1 rs2237895 with T2DM and provide reliable evidence for genetic susceptibility to T2DM.
We searched PubMed, Embase, Web of Science, Cochrane Library, Medline, Baidu Academic, China National Knowledge Infrastructure, China Biomedical Liter-ature Database, and Wanfang to investigate the association between KCNQ1 gene rs2237895 and the risk of T2DM up to January 12, 2022. Review Manager 5.4 was used to analyze the association of the KCNQ1 gene rs2237895 polymorphism with T2DM and to evaluate the publication bias of the selected literature.
Twelve case–control studies (including 11273 cases and 11654 controls) met our inclusion criteria. In the full population, allelic model [odds ratio (OR): 1.19; 95% confidence interval (95%CI): 1.09–1.29; P < 0.0001], recessive model (OR: 1.20; 95%CI: 1.11–1.29; P < 0.0001), dominant model (OR: 1.27. 95%CI: 1.14–1.42; P < 0.0001), and codominant model (OR: 1.36; 95%CI: 1.15–1.60; P = 0.0003) (OR: 1.22; 95%CI: 1.10–1.36; P = 0.0002) indicated that the KCNQ1 gene rs2237895 polymorphism was significantly correlated with susceptibility to T2DM. In stratified analysis, this association was confirmed in Asian populations: allelic model (OR: 1.25; 95%CI: 1.13–1.37; P < 0.0001), recessive model (OR: 1.29; 95%CI: 1.11–1.49; P = 0.0007), dominant model (OR: 1.35; 95%CI: 1.20–1.52; P < 0.0001), codominant model (OR: 1.49; 95%CI: 1.22–1.81; P < 0.0001) (OR: 1.26; 95%CI: 1.16–1.36; P < 0.0001). In non-Asian populations, this association was not significant: Allelic model (OR: 1.06, 95%CI: 0.98–1.14; P = 0.12), recessive model (OR: 1.04; 95%CI: 0.75–1.42; P = 0.83), dominant model (OR: 1.06; 95%CI: 0.98–1.15; P = 0.15), codominant model (OR: 1.08; 95%CI: 0.82–1.42; P = 0.60. OR: 1.15; 95%CI: 0.95–1.39; P = 0.14).
KCNQ1 gene rs2237895 was significantly associated with susceptibility to T2DM in an Asian population. Carriers of the C allele had a higher risk of T2DM. This association was not significant in non-Asian populations.
Core Tip: In Asian populations, the rs2237895 polymorphism in the KCNQ1 gene was significantly associated with susceptibility to type 2 diabetes mellitus (T2DM), and C allele carriers had an increased risk of developing T2DM. The CC and AC genotypes of KCNQ1 rs2237895 significantly increased the susceptibility to T2DM. In non-Asian populations, this association was not significant.