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CYP11B1 gene polymorphisms and susceptibility to ischemic stroke in a Chinese Han population
1Department of Critical Care Medicine, Xianyang Central Hospital, Xianyang, China.
Insights
CYP11B1 gene polymorphisms impact ischemic stroke (IS) risk. Specific single nucleotide polymorphisms (SNPs) like rs5283 increase IS susceptibility, while others like rs6410 offer protection in the Chinese Han population.
Area of Science:
- Genetics
- Neurology
- Molecular Biology
Background:
- Ischemic stroke (IS) is a leading cause of death and disability worldwide.
- Previous research has indicated a link between the CYP11B1 gene and IS.
- The specific impact of CYP11B1 gene polymorphisms on IS susceptibility requires further investigation.
Purpose of the Study:
- To analyze the association between CYP11B1 gene polymorphisms and ischemic stroke (IS) susceptibility.
- To investigate the roles of specific single nucleotide polymorphisms (SNPs) within the CYP11B1 gene in relation to IS risk.
- To explore SNP-SNP interactions influencing IS development.
Main Methods:
- Genotyping of six CYP11B1 SNPs (rs4736312, rs5017238, rs5301, rs5283, rs6410, and rs4534) in peripheral blood samples.
- Logistic regression analysis to assess the association between SNPs and IS risk.
- Multifactor dimensionality reduction (MDR) to identify SNP-SNP interactions.
Main Results:
- The SNP rs5283 was associated with increased IS susceptibility (OR 1.81, p=0.012).
- The SNP rs6410 demonstrated a protective effect against IS risk (OR 0.56, p=0.020).
- Stratified analyses revealed specific demographic and clinical factors influencing the risk associated with rs5283 and rs6410, with rs5283 identified as the best predictive model for IS via MDR analysis.
Conclusions:
- CYP11B1 gene polymorphisms are significantly correlated with ischemic stroke (IS) susceptibility.
- Specific SNPs within CYP11B1, such as rs5283 and rs6410, play distinct roles in IS risk.
- These findings contribute to understanding the genetic basis of IS in the Chinese Han population.
Objectives:
Ischemic stroke (IS) is the major cause of death and disability. While previous studies confirmed that CYP11B1 is closely associated with IS, the present study aimed to analyze the impact of CYP11B1 gene polymorphisms on the IS susceptibility.
Methods:
The present study genotyped six single nucleotide polymorphisms (SNPs) (including rs4736312, rs5017238, rs5301, rs5283, rs6410, and rs4534) of CYP11B1 in peripheral blood samples from IS and control populations. Logistic regression analysis was used to analyze the association between the SNPs and IS risk. The multifactor dimensionality reduction (MDR) method was used to determine the roles of SNP-SNP interactions in IS.
Results:
The present study showed that rs5283 was associated with an increased susceptibility to IS [odds ratio (OR) 1.81, p = 0.012]. On the contrary, rs6410 had a protective influence on IS risk (OR 0.56, p = 0.020). Stratified analyses indicated that rs5283 could enhance the risk of IS in subjects aged >63 years (OR 2.41, p = 0.011), of female gender (OR 3.31, p = 0.001), that do not smoke (OR 1.64, p = 0.005), and with hypertension (OR 2.07, p = 0.003). Whereas, rs6410 was related to a lower susceptibility to IS in subjects aged >63 years (OR 0.43, p = 0.032), of female gender (OR 0.30, p = 0.006), do not smoke (OR 0.42, p = 0.017), and with hypertension (OR 0.52, p = 0.022). Besides, rs4736312 reduced the IS susceptibility in non-smokers (OR 0.69, p = 0.031). Rs4534 had a risk-decreasing impact on IS in non-drinking (OR 0.54, p = 0.016). Moreover, the results of the MDR analysis corroborate that the best prediction model for IS was rs5283.
Conclusion:
This study revealed that CYP11B1 gene polymorphisms strongly correlated with IS in the Chinese Han population.
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