Stein Catherine M, Zalwango Sarah, Chiunda Allan B, Millard Christopher, Leontiev Dmitry V, Horvath Amanda L, Cartier Kevin C, Chervenak Keith, Boom W Henry, Elston Robert C, Mugerwa Roy D, Whalen Christopher C, Iyengar Sudha K
Department of Epidemiology and Biostatistics, Case Western Reserve University, Wolstein Research Building Room 1303, 2103 Cornell Rd, Cleveland, OH 44106, USA.
Hum Genet. 2007 Jul;121(6):663-73. doi: 10.1007/s00439-007-0357-8. Epub 2007 Apr 13.
Tuberculosis (TB) is a growing public health threat globally and several studies suggest a role of host genetic susceptibility in increased TB risk. As part of a household contact study in Kampala, Uganda, we have taken a unique approach to the study of genetic susceptibility to TB by developing an intermediate phenotype model for TB susceptibility, analyzing levels of tumor necrosis factor-alpha (TNFalpha) in response to culture filtrate as the phenotype. In the present study, we analyzed candidate genes related to TNFalpha regulation and found that interleukin (IL)-10, interferon-gamma receptor 1 (IFNGR1), and TNFalpha receptor 1 (TNFR1) genes were linked and associated to both TB and TNFalpha. We also show that these associations are with progression to active disease and not susceptibility to latent infection. This is the first report of an association between TB and TNFR1 in a human population and our findings for IL-10 and IFNGR1 replicate previous findings. By observing pleiotropic effects on both phenotypes, we show construct validity of our intermediate phenotype model, which enables the characterization of the role of these genetic polymorphisms on TB pathogenesis. This study further illustrates the utility of such a model for disentangling complex traits.
结核病(TB)在全球范围内对公共卫生构成的威胁日益严重,多项研究表明宿主遗传易感性在结核病风险增加中发挥作用。作为乌干达坎帕拉一项家庭接触者研究的一部分,我们采用了一种独特的方法来研究结核病的遗传易感性,即通过建立结核病易感性的中间表型模型,将对培养滤液产生反应时的肿瘤坏死因子-α(TNFα)水平作为表型进行分析。在本研究中,我们分析了与TNFα调节相关的候选基因,发现白细胞介素(IL)-10、干扰素-γ受体1(IFNGR1)和TNFα受体1(TNFR1)基因与结核病和TNFα均相关联。我们还表明,这些关联与进展为活动性疾病有关,而与潜伏感染易感性无关。这是关于人类群体中结核病与TNFR1之间关联的首次报告,我们关于IL-10和IFNGR1的研究结果重复了先前的发现。通过观察对两种表型的多效性作用,我们展示了中间表型模型的构建效度,该模型能够描述这些基因多态性在结核病发病机制中的作用。这项研究进一步说明了这种模型在解析复杂性状方面的实用性。