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

2018 ◽  
Vol 65 (3) ◽  
Author(s):  
Elena Kazakova ◽  
Meijun Chen ◽  
Esma Jamaspishvili ◽  
Zhang Lin ◽  
Jingling Yu ◽  
...  

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.

2020 ◽  
Author(s):  
Li Jin ◽  
Yan Huang ◽  
Yangyang Li ◽  
Bo Xu ◽  
Cheng Hu ◽  
...  

Abstract Background: CYP2C8 and CYP2C9 are cytochrome P450 epoxygenases that metabolize arachidonic acid into epoxyeicosatrienoic acids (EETs). EETs are important lipid mediators with many beneficial effects in type 2 diabetes mellitus. In this study, we aimed to investigate the association of CYP2C8 and CYP2C9 variants with type 2 diabetes in a Chinese population. Methods: We genotyped 9 tag single nucleotide polymorphisms (SNPs) in CYP2C8 and 10 tag SNPs in CYP2C9 based on HapMap Chinese and Japanese data. Then, we genotyped the SNPs in a Chinese population that included 3410 type 2 diabetes patients and 3401 normal controls. The association between the SNPs and type 2 diabetes was analysed. Results: In the study population, we found that rs1819173 in the CYP2C9 gene region was associated with type 2 diabetes and the A allele was protective against type 2 diabetes (odds ratio: 0.840, 95% confidence interval (CI): 0.780-0.904, P=3.04×10-6). Haplotypes GT and AT (rs2071426-rs6583967) in CYP2C8 were associated with type 2 diabetes (P=0.049 and 0.038, respectively). On the other hand, an interaction effect between rs1819173 in CYP2C9 and rs12766752 in CYP2C8 on type 2 diabetes was found (P=0.003). What’s more, rs1819173 showed significant association with HDL-C (high-density lipoprotein cholesterol).Conclusions: Our results suggested that common SNPs in the CYP2C8 and CYP2C9 regions were associated with T2DM in a Chinese Han population.


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