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韩国人群缺血性中风的易感性与白细胞介素-1受体拮抗剂和肿瘤坏死因子-α基因的多态性有关,但与白细胞介素-1β基因无关。

Susceptibility for ischemic stroke in Korean population is associated with polymorphisms of the interleukin-1 receptor antagonist and tumor necrosis factor-alpha genes, but not the interleukin-1beta gene.

作者信息

Lee Byung-Cheol, Ahn Se-Young, Doo Ho-Kyung, Yim Sung-Vin, Lee Hee-Jae, Jin Sheng-Yu, Hong Seung-Jae, Lee Sang-Ho, Kim Sung-Do, Seo Jung-Chul, Leem Kang-Hyun, Chung Joo-Ho

机构信息

Department of Oriental Internal Medicine, College of Medicine, Kyung Hee University, 1 Hoegi-Dong, Dongdaemun-Ku, Seoul 130-701, South Korea.

出版信息

Neurosci Lett. 2004 Feb 26;357(1):33-6. doi: 10.1016/j.neulet.2003.12.041.

DOI:10.1016/j.neulet.2003.12.041
PMID:15036607
Abstract

Enhanced release of proinflammatory cytokines may contribute to the pathogenesis of ischemic stroke. Interleukin-1 receptor antagonist (IL-1Ra) is an anti-inflammatory cytokine, and tumor necrosis factor (TNF)-alpha and IL-1beta are proinflammatory cytokine. To determine the role of cytokines in genetic susceptibility to ischemic stroke, we genotyped ischemic stroke patients (n = 152) and the healthy control subjects (n = 165) for IL-1Ra, TNF-alpha and IL-1beta polymorphism by polymerase chain reaction-restriction fragment length polymorphism methods. The analysis shown the association of IL1RN1, IL1RN2 allele (IL1RN1, OR=0.44, P = 0.0206 IL1RN2, OR=2.90, P = 0.0141) and TNF1, TNF2 allele (TNF1, OR=2.16, P = 0.0225; TNF2, OR=2.16, P = 0.0225) to ischemic stroke. However, the genetic polymorphism of IL-1beta was not associated with ischemic stroke. Our results suggest that IL-1Ra and TNF-alpha gene polymorphism is associated with the susceptibility to ischemic stroke.

摘要

促炎细胞因子的释放增加可能与缺血性中风的发病机制有关。白细胞介素-1受体拮抗剂(IL-1Ra)是一种抗炎细胞因子,而肿瘤坏死因子(TNF)-α和IL-1β是促炎细胞因子。为了确定细胞因子在缺血性中风遗传易感性中的作用,我们采用聚合酶链反应-限制性片段长度多态性方法,对152例缺血性中风患者和165例健康对照者进行了IL-1Ra、TNF-α和IL-1β基因多态性的基因分型。分析显示IL1RN1、IL1RN2等位基因(IL1RN1,OR=0.44,P = 0.0206;IL1RN2,OR=2.90,P = 0.0141)以及TNF1、TNF2等位基因(TNF1,OR=2.16,P = 0.0225;TNF2,OR=2.16,P = 0.0225)与缺血性中风有关。然而,IL-1β的基因多态性与缺血性中风无关。我们的结果表明,IL-1Ra和TNF-α基因多态性与缺血性中风的易感性有关。

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