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 between the rs2237895 single nucleotide polymorphism (SNP) in the KCNQ1 gene and the prevalence of type 2 diabetes mellitus (T2DM) has been controversial in different studies.
The aim of this study was to investigate the association between the KCNQ1 gene rs2237895 and the prevalence of T2DM, and to provide help in establishing the pathogenesis of T2DM.
Demonstration of the association of the rs2237895 SNP in the KCNQ1 gene with the prevalence of T2DM. Also, to explore whether this relationship differs in different populations.
We searched nine databases. Two authors independently screened the literature according to the established inclusion and exclusion criteria. Finally, data extraction was performed and the data were meta-analyzed.
Twelve case–control studies met our inclusion criteria. After analysis, the rs2237895 SNP in the KCNQ1 gene was associated with T2DM prevalence in Asian populations. However, this association was not significant in non-Asian populations.
In Asian populations, carriers of the rs2237895 C allele of the KCNQ1 gene were highly susceptible to T2DM compared to those who did not carry the C allele. However, in non-Asian populations, the association between the rs2237895 SNP and T2DM was not significant.
We should continue to search for T2DM susceptibility genes through advanced technologies (e.g., genome-wide association strategy) and gradually elucidate the pathogenesis of T2DM.
