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诱导型一氧化氮合酶基因的多态性与结核病相关。

A polymorphism in the inducible nitric oxide synthase gene is associated with tuberculosis.

作者信息

Gómez Luis Miguel, Anaya Juan-Manuel, Vilchez José Ramón, Cadena Jose, Hinojosa Rosa, Vélez Luciano, Lopez-Nevot Miguel Angel, Martín Javier

机构信息

Cellular Biology and Immunogenetics Unit, Corporación para Investigaciones Biológicas (CIB), Cra. 72-A, No. 78-B-141, Medellín, Colombia.

出版信息

Tuberculosis (Edinb). 2007 Jul;87(4):288-94. doi: 10.1016/j.tube.2007.03.002. Epub 2007 May 2.

DOI:10.1016/j.tube.2007.03.002
PMID:17475563
Abstract

iNOS or NOS2 is a molecule that plays a key role in the immunological control of a broad spectrum of infectious agents. Investigation is hampered by difficulty in estimating in vivo production of nitric oxide (NO), but genetic studies provide a potential means of examining the relation between NO production and disease outcome. To better characterize the host genetic factors determining the susceptibility to TB, we evaluated the influence of two polymorphisms in the NOS2A gene on the risk of developing pulmonary TB in a Northwestern Colombian population, which is a moderately-high endemic area. One hundred and fourteen patients with TB and negative for human immunodeficiency virus, plus 304 healthy controls were examined for NOS2A CCTTT and TAAA polymorphisms. A total of 160 healthy controls mentioned before, underwent tuberculin skin test (TST). Analysis disclosed significant differences between patients and controls with NOS2A CCTTT polymorphism (P=0.0001, Pc=0.001, OR=0.4, and 95%CI=0.3-0.7) independent of TST status. When the NOS2A alleles were stratified into short (8-11) and long (12-16) repeats, significant differences with short repeats were observed between TB patients and all controls (P=0.005, OR=0.63, 95%CI=0.46-0.86). No individual association with NOS2A TAAA was detected. These results indicate that a polymorphism in the NOS2A gene influences the susceptibility to TB and suggest a role for NOS2A in the pathogenesis of mycobacterial infection.

摘要

诱导型一氧化氮合酶(iNOS)或一氧化氮合酶2(NOS2)是一种在多种感染因子的免疫控制中起关键作用的分子。由于难以估计体内一氧化氮(NO)的产生,研究受到阻碍,但基因研究提供了一种潜在手段来检验NO产生与疾病结局之间的关系。为了更好地表征决定结核病易感性的宿主遗传因素,我们评估了NOS2A基因中的两个多态性对哥伦比亚西北部人群患肺结核风险的影响,该地区是中度高发流行区。对114例人类免疫缺陷病毒阴性的结核病患者以及304名健康对照进行了NOS2A CCTTT和TAAA多态性检测。总共160名之前提到的健康对照接受了结核菌素皮肤试验(TST)。分析显示,无论TST状态如何,NOS2A CCTTT多态性的患者与对照之间存在显著差异(P = 0.0001,Pc = 0.001,OR = 0.4,95%CI = 0.3 - 0.7)。当将NOS2A等位基因分为短重复序列(8 - 11)和长重复序列(12 - 16)时,在结核病患者与所有对照之间观察到短重复序列存在显著差异(P = 0.005,OR = 0.63,95%CI = 0.46 - 0.86)。未检测到与NOS2A TAAA的个体关联。这些结果表明,NOS2A基因中的多态性影响结核病易感性,并提示NOS2A在分枝杆菌感染的发病机制中起作用。

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