Association between RBMS1 gene rs7593730 and BCAR1 gene rs7202877 and Type 2 Diabetes Mellitus in a Chinese Han Population

Elena Kazakova; Meijun Chen; Esma Jamaspishvili; Zhang Lin; Jingling Yu; Lulu Sun; Hong Qiao

doi:10.18388/abp.2017_1451

Elena Kazakova Department of Endocrinology and Metabolism, the Second Affiliated Hospital, Harbin Medical University, Harbin, Heilongjiang, China
Meijun Chen Department of Endocrinology and Metabolism, the Second Affiliated Hospital, Harbin Medical University, Harbin, Heilongjiang, China
Esma Jamaspishvili Department of Endocrinology and Metabolism, the Second Affiliated Hospital, Harbin Medical University, Harbin, Heilongjiang, China
Zhang Lin Department of Endocrinology and Metabolism, the Second Affiliated Hospital, Harbin Medical University, Harbin, Heilongjiang, China;
Jingling Yu General Hospital of Jixi Mining Group, Jixi, Heilongjiang, China
Lulu Sun Department of Endocrinology and Metabolism, the Second Affiliated Hospital, Harbin Medical University, Harbin, Heilongjiang, China
Hong Qiao Department of Endocrinology and Metabolism, the Second Affiliated Hospital, Harbin Medical University, Harbin, Heilongjiang, China

DOI: https://doi.org/10.18388/abp.2017_1451

Abstract

Two recent studies found that RBMS1 gene rs7593730 and BCAR1 gene rs7202877 had relationships with type 2 diabetes. However, the association of these loci with type 2 diabetes mellitus (T2DM) has not been examined in Chinese. We performed a replication study to investigate the association of 2 susceptibility loci with T2DM in the Chinese population. We genotyped 1961 Chinese participants (991 with T2DM and 970controls) for each of the 2 single nucleotide polymorphisms (SNPs) rs7593730 in RBMS1 and rs7202877 near BCAR1 using SNPscan and examined the association of them with T2DM using logistic regression analysis. We also analyzed the correlation of the SNP allele and clinical phenotypes. In additive model, genotype association analysis of BCAR1 rs7202877 loci revealed that the homozygous of rs7202877 GG carriers had a significant decreased T2DM risk compared to homozygous carriers of TT (p= 0.038, OR 0.44, 95 % CI 0.20-0.96). In the recessive model, the genotype GG carriers had a significant decreased T2DM risk compared to GT+TT (p= 0.043, OR 0.67, 95% CI 0.46-0.99). Allele G was statistically significantly correlated with TC (mmol/L) (P=0.036) and LDL-C (mmol/L) (P=0.007). As for rs7593730, the carriers of genotype CT and TT had significantly decreased T2DM risk compared with the carriers of genotype CC (CT: CC P=0.038, OR 0.71, 95%CI 0.51-0.98; TT: CC P=0.010, OR 0.32, 95%CI 0.13-0.76). In a dominant model, TT+CT: CC (p= 0.013, OR 0.673, 95 % CI 0.49-0.92) and in a recessive model, TT: CT+CC (p= 0.019, OR 0.59, 95% CI 0.39-0.92). The T allele carriers had a significant decreased T2DM risk compared to carriers of C (p= 0.002, OR 0.65, 95 % CI 0.50-0.86). Allele T was statistically correlated with FINS (P=0.010). In conclusion, our study showed that RBMS1 gene rs7593730 and BCAR1 gene rs7202877 were significantly associated with type 2 diabetes in the Chinese population.