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The association analysis between CYP24A1 genetic polymorphisms and the risk of ischemic stroke in Chinese Han population.

Authors :
Yang, Wei
Ma, Fenghui
Wang, Li
He, Xue
Zhang, Hengxun
Zheng, Jianwen
Wang, Yuhe
Jin, Tianbo
Yuan, Dongya
He, Yongjun
Source :
Brain & Behavior. Feb2020, Vol. 10 Issue 2, pN.PAG-N.PAG. 1p.
Publication Year :
2020

Abstract

Aims: Stroke is a complicated neurological disease and the second leading cause of death in the world. We aimed to investigate the association between CYP24A1 genetic polymorphisms and ischemic stroke risk. Methods: In this case–control study, four single‐nucleotide polymorphisms of CYP24A1 were selected and genotyped by MassARRAY platform in Chinese Han population. Odds ratios and 95% confidence intervals were calculated via logistic regression analysis with adjustment in genetic models. Results: Our results indicated that CYP24A1 variant (rs1570669) was associated with the decreased risk of ischemic stroke (OR = 0.60, p <.001). Stratification analysis showed that the rs6068816 could enhance the ischemic stroke risk by 1.64 times (OR = 1.64, p =.028), while rs1570669 played protective role (OR = 0.63, p =.044) in age >64 years. The rs2762934 had an increased ischemic stroke susceptibility (OR = 1.62, p =.033); however, rs1570669 might reduce stroke risk (OR = 0.61, p =.015) in age ≤64 years. The rs1570669 depressed ischemic stroke susceptibility both in female and male patients (OR = 0.46, p =.002; OR = 0.69, p =.033, respectively), and rs2296241 would weaken the risk in male (OR = 0.63, p =.012). The rs1570669 was associated with decreased risk of ischemic stroke with hypertension (OR = 0.56, p =.042). Conclusion: Our study gave the evidences that CYP24A1 genetic polymorphisms were significantly associated with ischemic stroke patients, which would provide useful information of assessment or possible diagnostic markers for ischemic stroke. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
21623279
Volume :
10
Issue :
2
Database :
Academic Search Index
Journal :
Brain & Behavior
Publication Type :
Academic Journal
Accession number :
141660432
Full Text :
https://doi.org/10.1002/brb3.1503