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纤溶酶原激活物抑制剂 1 基因 4G/5G 多态性与韩国女性高血压的关系。

Relationship of plasminogen activator inhibitor 1 gene 4G/5G polymorphisms to hypertension in Korean women.

机构信息

Department of Family Practice and Community Health, Ajou University School of Medicine, Suwon, Republic of Korea.

出版信息

Chin Med J (Engl). 2012 Apr;125(7):1249-53.

PMID:22613596
Abstract

BACKGROUND

Hypertension (HTN) is a major determinant of various cardiovascular events. Plasma levels of plasminogen activator inhibitor 1 (PAI-1) modulate this risk. A deletion/insertion polymorphism within the PAI-1 loci (4G/4G, 4G/5G, 5G/5G) affects the expression of this gene. The present study investigated the association between PAI-1 loci polymorphisms and HTN in Korean women.

METHODS

Korean women (n = 1312) were enrolled in this study to evaluate the association between PAI-1 4G/5G gene polymorphisms and HTN as well as other metabolic risk factors. PAI-1 loci polymorphisms were investigated using polymerase chain reaction amplification and single-strand conformation polymorphism analysis.

RESULTS

The three genotype groups differed with respect to systolic blood pressure (P = 0.043), and diastolic blood pressure (P = 0.009) but not with respect to age, body mass index, total cholesterol, low or high density lipoprotein cholesterol, triglycerides, or fasting blood glucose. Carriers of the PAI-1 4G allele had more hypertension significantly (PAI-1 4G/5G vs. PAI-1 5G/5G, P = 0.032; PAI-1 4G/4G vs. PAI-1 5G/5G, P = 0.034). When stratified according to PAI-1 4G/5G polymorphism, there was no significant difference in all metabolic parameters among PAI-1 genotype groups in patients with HTN as well as subjects with normal blood pressure. The estimated odds ratio of the 4G/4G genotype and 4G/5G for HTN was 1.7 (P = 0.005), and 1.6 (P = 0.015), respectively.

CONCLUSION

These findings might indicate that PAI-1 loci polymorphisms independently contribute to HTN and that gene-environmental interaction may be not associated in Korean women.

摘要

背景

高血压(HTN)是各种心血管事件的主要决定因素。纤溶酶原激活物抑制剂 1(PAI-1)的血浆水平调节这种风险。PAI-1 基因座内的缺失/插入多态性(4G/4G、4G/5G、5G/5G)影响该基因的表达。本研究调查了韩国女性 PAI-1 基因座多态性与 HTN 之间的关系。

方法

本研究纳入了 1312 名韩国女性,以评估 PAI-1 4G/5G 基因多态性与 HTN 以及其他代谢危险因素之间的关系。使用聚合酶链反应扩增和单链构象多态性分析来研究 PAI-1 基因座多态性。

结果

三组基因型在收缩压(P=0.043)和舒张压(P=0.009)方面存在差异,但在年龄、体重指数、总胆固醇、低或高密度脂蛋白胆固醇、甘油三酯或空腹血糖方面没有差异。PAI-1 4G 等位基因携带者的高血压发生率显著更高(PAI-1 4G/5G 与 PAI-1 5G/5G,P=0.032;PAI-1 4G/4G 与 PAI-1 5G/5G,P=0.034)。根据 PAI-1 4G/5G 多态性分层,高血压患者和血压正常患者的 PAI-1 基因型组之间在所有代谢参数方面均无显著差异。4G/4G 基因型和 4G/5G 基因型发生 HTN 的估计比值比分别为 1.7(P=0.005)和 1.6(P=0.015)。

结论

这些发现可能表明 PAI-1 基因座多态性独立导致 HTN,并且在韩国女性中基因-环境相互作用可能不相关。

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