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Polymorphisms in interferon pathway genes and risk of Mycobacterium tuberculosis infection in contacts of tuberculosis cases in Brazil

机译:干扰素途径基因的多态性以及结核病患者结核病患者结核病患者的特征性途径

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Background Host genetic polymorphisms may be important in determining susceptibility to Mycobacterium tuberculosis (Mtb) infection, but their role is not fully understood. Detection of microbial DNA and activation of type I interferon (IFN) pathways regulate macrophage responses to Mtb infection. Methods We examined whether seven candidate gene SNPs were associated with tuberculin skin test (TST) positivity in close contacts of microbiologically confirmed pulmonary TB patients in Brazil. Independent associations with TST positivity were tested using multivariable logistic regression (using genotypes and clinical variables) and genetic models. Results Among 482 contacts of 145 TB index cases, 296 contacts were TST positive. Multivariable regression analysis adjusted for population admixture, age, family relatedness, sex and clinical variables related to increased TB risk demonstrated that SNPs in PYHIN1-IFI16-AIM2 rs1101998 (adjusted OR [aOR]: 3.72; 95%CI?=?1.15–12.0; p?=?0.028) and in PYHIN1-IFI16-AIM2 rs1633256 (aOR?=?24.84; 95%CI?=?2.26–272.95; p?=?0.009) were associated with TST positivity in a recessive model. Furthermore, an IRF7 polymorphism (rs11246213) was associated with reduced odds of TST positivity in a dominant model (aOR: 0.50, 95%CI: 0.26-0.93; p?=?0.029). Conclusions Polymorphisms in PYHIN1- IFI16 -AIM2 rs1633256, rs1101998 and in IRF7 rs11246213 were associated with altered susceptibility to Mtb infection in this Brazilian cohort.
机译:背景宿主遗传多态性对于确定对结核病(MTB)感染的易感性来说可能是重要的,但它们的作用尚不完全理解。微生物DNA的检测和I型干扰素(IFN)途径的激活调节对MTB感染的巨噬细胞反应。方法检查七个候选基因SNP是否与患者在巴西微生物学证实肺结核患者的密闭接触中与结核病皮肤测试(TST)积极性有关。使用多变量逻辑回归(使用基因型和临床变量)和遗传模型来测试与TST阳性的独立关联。结果482个触点145 TB指数案例中,296个触点是TST阳性。多变量的回归分析适用于群体混合物,年龄,家庭相关性,性别和临床变量,与增加的结核病风险增加展示了SNPS在Pyhin1-IFI16-AIM2 RS1101998中(调整或[AOR]:3.72; 95%CI?=?1.15-12.0 ; p?= 0.028)和Pyhin1-IFI16-AIM2 RS1633256(AOR?= 24.84; 95%CI?=?2.26-272.95; p?= 0.009)与隐性模型中的TST阳性相关。此外,IRF7多态性(RS11246213)与优势模型中的TST阳性的几率降低有关(AOR:0.50,95%CI:0.26-0.93; P?= 0.029)。结论PYHIN1-IFI16 -AMAM2 RS1633256,RS1101998和IRF7 RS11246213中的多态性与该巴西队列中的MTB感染的易感性改变了。

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