Associations of CKIP-1 and LOX-1 polymorphisms with the risk of type 2 diabetes mellitus with hypertension among Chinese adults

Aims Type 2 diabetes mellitus (T2DM) and hypertension are common high-incidence diseases, closely related, and have common pathogenic basis such as oxidative stress. Casein kinase 2 interacting protein-1 ( CKIP-1 ) and low-density lipoprotein receptor ( LOX-1 ) are considered to be important factors affect the level of oxidative stress in the body. The main purpose of this study was to explore the relationship between CKIP-1 (rs6693817 A > T, rs2306235 C > G) and LOX-1 (rs1050283 G > A, rs11053646 C > G) polymorphisms and the risk of hypertension and diabetes, and try to find new candidate genes for diabetes and diabetes with hypertension etiology in Chinese population. Methods 574 T2DM patients and 597 controls frequently matched by age and sex were selected for genotyping of CKIP-1 (rs6693817 A > T, rs2306235 C > G) and LOX-1 gene (rs1050283 G > A, rs11053646 C > G). Logistic regression was used to analyze the correlation between different genotypes and the risk of T2DM and T2DM with hypertension, and the results were expressed as odds ratio ( OR ) and 95% confidence interval (95% CI ). Results We found that the risk of T2DM in the AA + AT genotype of rs6693817 was higher than that in the TT genotype in Chinese population ( OR = 1.318, 95% CI : 1.011–1.717, P = 0.041), and the difference was still significant after adjustment ( OR = 1.370, 95% CI : 1.043–1.799, P adjusted = 0.024), the difference of heterozygotes (AT vs TT: OR = 1.374, 95% CI : 1.026–1.840, P adjusted = 0.033) was statistically significant. But after Bonferroni correction, the significance of the above sites disappeared. And rs6693817 was associated with the risk of T2DM combined with hypertension before and after adjustment in dominant model ( OR = 1.424, 95% CI : 1.038–1.954, P = 0.028; OR = 1.460, 95% CI : 1.057–2.015, P adjusted = 0.021, respectively) and in heterozygote model ( OR = 1.499, 95% CI : 1.069–2.102, P = 0.019; OR = 1.562, 95% CI : 1.106–2.207, P adjusted = 0.011, respectively). However, only the statistical significance of the heterozygous model remained after Bonferroni correction. rs2306235, rs1050283 and rs11053646 were not significantly correlated with T2DM and T2DM combined with hypertension risk ( P > 0.05). Conclusions The results suggest that CKIP-1 rs6693817 is related to the susceptibility of Chinese people to T2DM with hypertension, providing a new genetic target for the treatment of diabetes with hypertension with in the future.