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    This study aimed to explore the association between genetic variations of CYP19A1 and stroke susceptibility in the Chinese Han population. A total of 477 stroke patients and 480 healthy controls were recruited in this study. The genotyping of CYP19A1 polymorphisms (rs4646, rs6493487, rs1062033, rs17601876, and rs3751599) was performed by the Agena MassARRAY platform. Under logistic regression models, we evaluated the associations of CYP19A1 polymorphisms and stroke susceptibility by odds ratio and 95% confidence interval. Our study showed that rs4646 (codominant: P = 0.020; recessive: P = 0.016) and rs17601876 (allele: P = 0.044; codominant: P = 0.011; dominant: P = 0.009; recessive: P = 0.046) significantly decreased the risk of stroke. In the stratification analysis, rs4646 is associated with decreased stroke risk among the individuals older than 64 years (codominant: P = 0.028; recessive: P = 0.010) and women (codominant: P = 0.029; recessive: P = 0.029), whereas rs1062033 increased stroke risk in the subgroup of age 64 years and younger (recessive: P = 0.042). The rs17601876 polymorphism has a strong relationship with stroke susceptibility, which is age and gender dependent. In haplotype analysis, we found a block (rs17601876 and rs3751599), and Ars17601876Grs3751599 haplotype is related to an increased stroke risk (P < 0.05). In addition, CYP19A1 variations had effects on clinical characteristics. CYP19A1 polymorphisms were significantly associated with stroke susceptibility in the Chinese Han population.


    Qing Cai, Jianwen Zheng, Mei Bai, Xue He, Li Wang, Yongjun He, Dongya Yuan, Tingqin Huang, Junjie Zhao, Yuan Wu, Xudong Ma, Ming Zhang, Tianbo Jin, Guodong Gao. Genetic Variations of CYP19A1 Gene and Stroke Susceptibility: A Case-Control Study in the Chinese Han Population. Journal of cardiovascular pharmacology. 2020 Apr;75(4):344-350

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    PMID: 31895872

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