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对氧磷酶1基因Q192R多态性与青年缺血性脑卒中的关系

[Relationship between Q192R polymorphisms in paraoxonase 1 gene and young ischemic stroke].

作者信息

Liu Jing-li, Li Jin-pin, Wang Xiao-ling, Yang Yi

机构信息

Department of Neurology, First Affiliated Hospital, Guangxi Medical University, Nanning 530021, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2010 Apr 6;90(13):912-6.

Abstract

OBJECTIVE

To investigate the relationship between polymorphisms in paraoxonase1 (PON1) gene Gln192Arg (Q192R) and arterial ischemic stroke in young adults.

METHODS

The Q192R genotype was analyzed by polymerase chain reaction in 131 young adults with ischemic stroke and 135 age- and gender-matched controls. The plasma lipids were also determined in patients and controls respectively. Furthermore, carotid artery intima-media thickness (IMT) in patients were measured by carotid ultrasonography.

RESULTS

The distributions of Q192R genotype frequency were significantly different between patients with ischemic stroke and control individuals. And the patients had more RR genotypes than control individuals (P < 0.05). Odds ratio (OR) for stroke were 1.743 (95% confidence interval [CI], 1.032-2.943) in subjects with RR genotype. We also studied the relationship between the polymorphisms and the lipid concentration in patients and control individuals. However, no significant association was detected between Q/R192 genotype and any of lipid measurements. Further, the prevalence of cigarette smoking, hypertension and diabetes showed no significant difference between RR and non-RR genotypes in patients. Body mass index (BMI) in two groups did not differ significantly. But IMT of patients with RR genotype obviously increased in comparison to those without RR genotype (P < 0.05).

CONCLUSION

The PON1 gene Q192R polymorphism may be associated with the susceptibility of ischemic stroke in young adults. RR genotype is a genetic risk for young adults with ischemic stroke through an increased carotid artery intima-media thickness and an accelerated atherosclerotic process.

摘要

目的

探讨对氧磷酶1(PON1)基因Gln192Arg(Q192R)多态性与青年动脉缺血性卒中的关系。

方法

采用聚合酶链反应分析131例青年缺血性卒中患者及135例年龄、性别匹配的对照者的Q192R基因型。分别测定患者和对照者的血脂。此外,采用颈动脉超声测量患者的颈动脉内膜中层厚度(IMT)。

结果

缺血性卒中患者与对照者的Q192R基因型频率分布有显著差异。患者的RR基因型多于对照者(P<0.05)。RR基因型受试者发生卒中的比值比(OR)为1.743(95%置信区间[CI],1.032 - 2.943)。我们还研究了患者和对照者中多态性与血脂浓度的关系。然而,未检测到Q/R192基因型与任何血脂指标之间存在显著关联。此外,患者中RR和非RR基因型在吸烟、高血压和糖尿病患病率方面无显著差异。两组的体重指数(BMI)无显著差异。但RR基因型患者的IMT明显高于非RR基因型患者(P<0.05)。

结论

PON1基因Q192R多态性可能与青年缺血性卒中的易感性有关。RR基因型通过增加颈动脉内膜中层厚度和加速动脉粥样硬化进程,成为青年缺血性卒中患者的遗传风险因素。

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