Association between cannabinoid receptor-1 gene polymorphism and the risk of diabetic nephropathy among patients with type 2 diabetes mellitus

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Abstract

Background: The cannabinoid receptor 1 (CNR1) gene polymorphism is reportedly associated with components of metabolic syndrome and coronary artery diseases in patients with type 2 diabetes mellitus (T2DM). We investigated whether the common variant rs10493353 polymorphism is associated with diabetic nephropathy (DN) in T2DM patients. Patients and Methods: T2DM patients with DN were enrolled as a case group, and patients with only T2DM as a control group. Demographic data and biochemical parameters were collected. The polymerase chain reaction-based restriction fragment length polymorphism technique was used for genotyping. The odds ratio and 90% confidence interval were calculated to assess the association between genotypes and the risk of DN. Results: In total, 320 T2DM patients and 320 DN patients were enrolled. Compared with T2DM patients, the DN patients have a significantly larger body mass index (BMI), longer duration of disease, and higher proportions of smokers, drinkers, and hypertension. The risk of DN was significantly decreased by genotypes AA (OR=0.39, 95% CI=0.23–0.67) and GA (OR=0.53, 95% CI=0.37–0.75) vs GG (codominant model), GA/AA vs GG (OR=0.49, 95% CI=0.35–0.67; dominant model), AA vs GG/GA (OR=0.47, 95% CI=0.28–0.80; recessive model), and the A allele (OR=0.52, 95% CI=0.40–0.68; allele model). Multiple logistic regressions still show significant levels. Negative interactions were found between gene and clinical parameters, including drinking, smoking, BMI, and hypertension. Conclusion: The A allele of CNR1 gene rs10493353 may be a protective factor for DN in T2DM patients. The risk factors of DN can affect the protective role of A allele in the progression of DN.

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Zhang, X., Zhu, H., Xing, X., & Zhang, C. (2020). Association between cannabinoid receptor-1 gene polymorphism and the risk of diabetic nephropathy among patients with type 2 diabetes mellitus. Pharmacogenomics and Personalized Medicine, 13, 591–599. https://doi.org/10.2147/PGPM.S278897

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