北印度人群细胞色素P450 G1347A基因多态性与缺血性卒中风险的关系:一项病例对照研究

Ram Sagar, Amit Kumar, S. Misra, Pradeep Kumar, R. Raj, A. Gulati, K. Prasad
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引用次数: 1

摘要

目的:本研究旨在建立CYP4F2 G1347A多态性与北印度人群缺血性卒中(IS)风险之间的关系。方法:在一项以医院为基础的病例对照研究中,从印度新德里全印度医学科学研究所神经内科门诊招募了250例病例和250例年龄和性别匹配的对照受试者。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)进行基因分型。数据分析使用STATA软件,版本13。结果:IS患者平均年龄为52.83±12.59岁,对照组平均年龄为50.97±12.70岁。在病例和对照组中,基因型频率分布符合Hardy Weinberg平衡(HWE)。条件logistic回归分析显示,显性模型下CYP450 G1347A基因多态性与IS风险独立相关(OR 2.05;95% CI 1.18 - 3.56)。基于Org 10172在急性卒中治疗(TOAST)分类中的试验分析发现,IS与大血管疾病(LVD)亚型在未调整(OR, 2.5;95% CI 1.49 - 4.20)和校正(OR, 3.32;95% CI 1.72 ~ 6.43),经调整分析后与IS的小血管病(SVD)亚型显著相关(OR, 2.43;95% CI 1.14 ~ 5.16)。结论:CYP4F2 G1347A多态性可能是IS的重要危险因素,主要是LVD亚型。需要大样本量的前瞻性研究来证实目前的发现。
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Relationship between Cytochrome P450 G1347A Gene Polymorphism and Risk of Ischemic Stroke in North Indian Population: A Case-Control Study
Objective: Present study was taken up to establish the association between CYP4F2 G1347A polymorphism and risk of ischemic stroke (IS) in a North Indian population. Methods: In a hospital-based case-control study, 250 cases and 250 age and sex matched control subjects were recruited from Outpatient Department of Neurology, All India Institute of Medical Sciences, New Delhi, India. Polymerase chain reaction – Restriction fragment length polymorphism (PCR-RFLP) was used for genotyping. Data were analyzed using STATA software, Version 13. Results: The mean age of IS patients were 52.83 ± 12.59 years and in control group were 50.97 ± 12.70 years. Genotypic frequency distributions were in accordance with Hardy Weinberg Equilibrium (HWE) in both cases and controls. Conditional logistic regression analysis showed an independent association between CYP450 G1347A gene polymorphism with the risk of IS under dominant model (OR 2.05; 95% CI 1.18 to 3.56). Analysis based on Trial of Org 10172 in Acute Stroke Treatment (TOAST) classification discerned a significant association with Large Vessel Disease (LVD) subtype of IS in both the unadjusted (OR, 2.5; 95% CI 1.49 to 4.20) and adjusted (OR, 3.32; 95% CI 1.72 to 6.43) analysis and a significant association with Small Vessel Disease (SVD) subtype of IS after the adjusted analysis (OR, 2.43; 95% CI 1.14 to 5.16) under recessive model. Conclusion: Present study suggests that CYP4F2 G1347A polymorphism may be an important risk factor for IS mainly for LVD subtype of IS. Prospective studies with large sample size are needed to confirm the present findings.
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