Back to Search Start Over

Effects of CASZ1, WNT2B and PTPRG SNPs on stroke susceptibility in the Chinese Han population.

Authors :
Zhang, Huan
Chang, Yanting
Li, Yujie
Wei, Jie
Ma, Xiaoya
Zhou, Wenqian
Zang, Xufeng
Jin, Tianbo
Wu, Songdi
Source :
European Journal of Clinical Investigation; Apr2024, Vol. 54 Issue 4, p1-12, 12p
Publication Year :
2024

Abstract

Background: Stroke is an important cause of death and disability worldwide, ranking second in the cause of death, and it is thought to be related to genetic factors. The purpose of our study is to investigate the association between CASZ1, WNT2B and PTPRG single nucleotide polymorphisms (SNPs) and stroke risk in the Chinese population. Methods: We recruited 1418 volunteers, comprised of 710 stroke cases and 708 controls in this study. We used MassARRAY iPLEX GOLD method to genotype the three SNPs on CASZ1, WNT2B and PTPRG. Logistic regression was used to analyse the association between these SNPs and stroke, and odds ratios (ORs) and 95% confidence intervals (CIs) were then calculated. What's more, the interactions among SNPs were predicted by multi‐factor dimensionality reduction (MDR) analysis. Results: This research demonstrated that CASZ1 rs880315 and PTPRG rs704341 were associated with reduced stroke susceptibility. More precisely, CASZ1 rs880315 was associated with reduced stroke susceptibility in people aged ≤64 years and women. PTPRG rs704341 was associated with reduced stroke susceptibility in people aged >64 years, women, non‐smokers and non‐drinkers. Conversely, WNT2B rs12037987 was related to elevated stroke susceptibility in people aged >64 years, women and non‐smokers. In addition, CASZ1 rs880315, WNT2B rs12037987 and PTPRG rs704341 had a strong redundancy relationship. Conclusion: Our study concludes that CASZ1 rs880315, WNT2B rs12037987 and PTPRG rs704341 are associated with stroke, and the study provides a basis for assessing genetic variants associated with stroke risk in the Han Chinese population. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00142972
Volume :
54
Issue :
4
Database :
Complementary Index
Journal :
European Journal of Clinical Investigation
Publication Type :
Academic Journal
Accession number :
175988713
Full Text :
https://doi.org/10.1111/eci.14144