NQO1 polymorphism and susceptibility to ischemic stroke in a Chinese population

Author:

Wang Min1,Shen Ying2,Gao Yuan3,Chen Huaqiu4,Duan Fuhui5,Li Siying5,Wang Guangming1

Affiliation:

1. Dali University

2. The First Hospital of Liangshan

3. Zhengzhou University

4. Xichang People’s Hospital

5. The First Affiliated Hospital of Dali University

Abstract

Abstract

Background Ischemic stroke (IS) is a major cause of death and disability worldwide. Genetic factors are important risk factors for the development of IS. The quinone oxidoreductase 1 gene (NQO1) has antioxidant, anti-inflammatory, and cytoprotective properties. Thus, in this study, we investigated the relationship between NQO1 gene polymorphism and the risk of IS. Methods Peripheral blood was collected from 143 patients with IS and 124 healthy controls in Yunnan, China, and NQO1 rs2917673, rs689455, and rs1800566 were genotyped. Logistic regression was used to analyze the relationship between the three NQO1 loci and IS susceptibility. The difference in the expression levels of NQO1 between the control and IS groups was verified using public databases and enzyme-linked immunosorbent assay. Results The rs2917673 locus increased the risk of IS by 2.375 times in TT genotype carriers under the co-dominance model compared with CC carriers and was statistically associated with the risk of IS (P = 0.046). In the recessive model, TT genotype carriers increased IS risk by 2.407 times compared with CC/CT carriers and were statistically associated with the risk of IS (P = 0.033). Conclusions NQO1 rs2917673 polymorphism is significantly associated with IS. Mutant TT carriers are risk factors for IS.

Publisher

Springer Science and Business Media LLC

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