Genetic variants in IFNG and IFNGR1 and tuberculosis susceptibility

Abstract

BackgroundTuberculosis (TB) is the type of chronic infectious disease which majorly caused by Mycobacterium tuberculosis (M. TB). Emerging data suggest that interferon gamma (IFNG) and its receptor IFNGR1 may be involved in the risk of TB. MethodsA total of 636 TB patients and 608 healthy controls were selected. The association between single nucleotide polymorphisms (SNPs) and TB was estimated by logistic analyses adjusting for age, gender and smoking status. SNPs genotyping was done by using the improved multiplex ligase detection reaction (iMLDR). ResultsThe IFNG rs1861494 allele C was related to an increased risk for TB (OR = 1.25, 95%CI: 1.06–1.48; P = 0.009). Compared with TT genotype, CT (OR = 1.28, 95%CI: 1.01–1.63; P = 0.040) and CC (OR = 1.51, 95%CI: 1.04–2.19; P = 0.031) were also risk factors for TB. In the subgroup analysis, the association was stronger among participants < 25 years (OR = 2.40, 95%CI: 1.70–3.38; P < 0.001) and male groups (OR = 1.31, 95%CI: 1.03–1.66; P = 0.030). In addition, IFNG rs1861494 was associated with anti-TB treatment outcome (OR = 0.70, 95%CI: 0.52–0.94; P = 0.017). We also detected that IFNGR1 rs2234711 influenced the IFNG production. ConclusionIFNG rs1861494 polymorphism was associated with TB, particularly in the younger and male subgroups.