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Chinese Journal of Antituberculosis ›› 2025, Vol. 47 ›› Issue (5): 629-638.doi: 10.19982/j.issn.1000-6621.20240592

• Original Articles • Previous Articles     Next Articles

Study on the association between single nucleotide polymorphisms in TMEM173,IFNGR1,IFNGR2, and IRF8 genes and susceptibility to tuberculosis

Huang Huimin1,2, Wang Lei2, Cheng Liping2, Sun Qin2, Wang Wenjuan1(), Yang Hua1,2()   

  1. 1School of Public Health, the Key Laboratory of Environmental Pollution Monitoring and Disease Control, Ministry of Education, Guizhou Medical University, Guiyang 561113, China
    2Shanghai Clinical Research Center of Infections Diseases (Tuberculosis), Shanghai Key Laboratory of Tuberculosis, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai 200433, China
  • Received:2024-12-27 Online:2025-05-10 Published:2025-04-29
  • Contact: Yang Hua,Email: yanghua97065@163.com;Wang Wenjuan,Email:reality0337@126.com E-mail:reality0337@126.com;yanghua97065@163.com
  • Supported by:
    National Key R&D Program of China(2021YFA1300902);National Natural Science Foundation of China(82470001);National Natural Science Foundation of China(82270006);National Natural Science Foundation of China(82070007);Youth Program of Shanghai Municipal Health Commission(20204Y0325)

Abstract:

Objective: To investigate the association between genetic polymorphisms in the stimulator of interferon genes (TMEM173), interferon gamma receptor 1 (IFNGR1), interferon gamma receptor 2 (IFNGR2), and interferon regulatory factor 8 (IRF8) and tuberculosis susceptibility. Methods: A case-control study was conducted, including 286 pulmonary tuberculosis cases (Observation group) admitted to Shanghai Pulmonary Hospital from January 2020 to December 2022 and 484 healthy individuals (Control group). Peripheral venous blood was collected from both groups for genomic DNA extraction, genetic analysis and single nucleotide polymorphism (SNP) screening. Genotyping was performed using the SNPscanTM multiplex SNP genotyping assay. Logistic regression and Chi-square tests were used to compare differences in allele, genotype, and haplotype frequencies between the observation and control groups. Associations between SNPs and tuberculosis susceptibility were analyzed under dominant, recessive, and over-dominant genetic models. Multivariate logistic regression was performed to analyze the association between the interaction among SNPs and tuberculosis susceptibility. Results: All SNP allele frequency distributions conformed to Hardy-Weinberg equilibrium. Carriers of the rs8064189 T allele (OR=1.290, 95%CI: 1.047-1.590, P=0.017), TT genotype (OR=1.689, 95%CI: 1.098-2.597, P=0.017), GT-TT genotype (ORdominant=1.231, 95%CI: 0.999-1.517, P=0.047) and rs805252 (OR=1.628, 95%CI: 1.033-2.565, P=0.035;ORrecessive=1.306, 95%CI: 1.037-1.645, P=0.037), as well as the CTGAA haploid type (OR=1.271, 95%CI: 1.078-1.513, P=0.011) of IRF8 gene significantly increased the tuberculosis risk. Rs9808753 AG genotype (OR=1.450, 95%CI: 1.038-2.025, P=0.029) and AA-GG genotype (ORhyper-dominance=0.807, 95%CI: 0.671-0.970, P=0.025) of IFNGR2 gene also significantly increased the risk of tuberculosis. The IFNGR1 TTGG haplotype (OR=1.160, 95%CI: 1.014-1.350, P=0.047) was linked to increased tuberculosis susceptibility. Multivariate logistic regression revealed that the CT genotype in TMEM173 gene rs7380824 increased the tuberculosis risk by 1.431-fold. (OR=1.431, 95%CI: 1.034-1.979, P=0.031). No significant associations were observed between tuberculosis susceptibility and other SNPs. Conclusion: TMEM173, IFNGR1, IFNGR2, and IRF8 genes may serve as susceptibility genes for tuberculosis in the Chinese population.

Key words: Tuberculosis, Gene, Polymorphisms, single nucleotides, Genetic predisposition to disease

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