伊朗东南部扎黑丹地区IFNGR1基因多态性与肺结核发病风险的关系

M. Naderi, M. Hashemi, M. Rezaei, A. Safdari
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引用次数: 14

摘要

的目标。本研究旨在发现干扰素-γ (IFN-γ)受体1 (IFNGR1)基因多态性与伊朗人群中肺结核(PTB)风险之间可能存在的关联。方法。在173例肺结核患者和164名健康受试者中检测到IFNGR1 rs1327474 (- 611 A/G)、rs11914 (+189 T/G)、rs7749390 (+95 C/T)和rs137854905 (27 bp ins/del)多态性。结果。我们的研究结果显示,与TT相比,rs11914 TG基因型降低了PTB的风险(OR = 0.36, 95% CI = 0.21-0.62, p = 0.0002)。与T等位基因相比,rs11914 G等位基因降低了PTB的风险(OR = 0.41, 95% CI = 0.25-0.68, p = 0.0006)。与CC基因型相比,IFNGR1 rs7749390 CT基因型降低了PTB的风险(OR = 0.55, 95% CI = 0.32-0.95, p = 0.038)。IFNGR1 rs1327474 A/G多态性与PTB发病风险/保护性无显著相关性。rs137854905 (27-bp I/D)在人群中不存在多态性。结论。我们的研究结果表明,IFNGR1 rs11914和rs7749390变异降低了我们人群中PTB易感性的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of Genetic Polymorphisms of IFNGR1 with the Risk of Pulmonary Tuberculosis in Zahedan, Southeast Iran
Aim. The present study was undertaken to find out the possible association between interferon-gamma (IFN-γ) receptor 1 (IFNGR1) gene polymorphisms and risk of pulmonary tuberculosis (PTB) in a sample of Iranian population. Methods. Polymorphisms of IFNGR1 rs1327474 (−611 A/G), rs11914 (+189 T/G), rs7749390 (+95 C/T), and rs137854905 (27-bp ins/del) were determined in 173 PTB patients and 164 healthy subjects. Results. Our findings showed that rs11914 TG genotypes decreased the risk of PTB in comparison with TT (OR = 0.36, 95% CI = 0.21–0.62, and p = 0.0002). The rs11914 G allele decreased the risk of PTB compared with T allele (OR = 0.41, 95% CI = 0.25–0.68, and p = 0.0006). IFNGR1 rs7749390 CT genotype decreased the risk of PTB in comparison with CC genotype (OR = 0.55, 95% CI = 0.32–0.95, and p = 0.038). No significant association was found between IFNGR1 rs1327474 A/G polymorphism and risk/protective of PTB. The rs137854905 (27-bp I/D) variant was not polymorphic in our population. Conclusion. Our findings showed that IFNGR1 rs11914 and rs7749390 variants decreased the risk of PTB susceptibility in our population.
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