Influence of Single-nucleotide Polymorphism of INF-γ (rs.2430561, +874 A/T) and Interleukin-10 (rs.1800896, -1082 A/G) on the Risk of Tuberculosis and Drug Resistance in Kaduna State, Nigeria.

IF 1.5 Q4 INFECTIOUS DISEASES
International Journal of Mycobacteriology Pub Date : 2025-04-01 Epub Date: 2025-06-20 DOI:10.4103/ijmy.ijmy_39_25
Suzie Madaki, Yusuf Mohammed, Lawal Dahiru Rogo, Mustapha Yusuf, Yazeed Garba Bala, Umar Aliyu Ahmad
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引用次数: 0

Abstract

Background: Tuberculosis (TB) remains a global health challenge, necessitating comprehensive research to understand genetic factors influencing susceptibility and drug resistance. This study aimed to investigate the presence of drug resistance, analyze single nucleotide polymorphisms (SNPs) in IFN-γ (reference SNP. 2430561, +874 Adenine/Thymine) and IL-10 (reference SNP.1800896, -1082 Adenine/Guanine), and assess their associations with age and sex among a cross section of TB patients in Kaduna state.

Methods: A total of 140 participants, comprising drug-resistant TB (DR-TB) patients, drug-susceptible TB (DS-TB) patients, and Apparently Healthy controls (AHCs), were enrolled. Genomic deoxyribonucleic acid was extracted, and SNPs were genotyped using polymerase chain reaction-based techniques. Associations between genotypes, alleles, age, and sex were analyzed. Odd ratios and Hardy-Weinberg equilibrium were employed for demographic and genetic analyses.

Results: In DR-TB, significant associations were observed between IFN-γ genotypes/alleles and increased susceptibility, with thymine thymine (TT) genotype and T allele showing higher frequency. For IL-10, guanine guanine (GG) genotype and G allele were prevalent, indicating potential associations with DR-TB risk. In DS-TB, similar trends were observed, highlighting potential genetic influences on susceptibility. HWE analysis revealed significant deviations in some groups, suggesting genetic variations.

Conclusions: The prevalence of specific genotypes and alleles indicates potential genetic markers for risk assessment. Deviations from HWE suggest population-specific genetic variations. These findings underscore the importance of genetic factors in TB outcomes and advocate for tailored interventions for different populations.

尼日利亚卡杜纳州INF-γ (rs.2430561, +874 A/T)和白细胞介素-10 (rs.1800896, -1082 A/G)单核苷酸多态性对结核病风险和耐药性的影响
背景:结核病(TB)仍然是一个全球性的健康挑战,有必要进行全面的研究,以了解影响易感性和耐药性的遗传因素。本研究旨在探讨耐药的存在,分析IFN-γ的单核苷酸多态性(SNP)(参考SNP)。2430561, +874腺嘌呤/胸腺嘧啶)和IL-10(参考SNP.1800896, -1082腺嘌呤/鸟嘌呤),并评估其与卡杜纳州结核患者横断面的年龄和性别的关系。方法:共纳入140名参与者,包括耐药结核病(DR-TB)患者、药敏结核病(DS-TB)患者和表面健康对照组(AHCs)。提取基因组脱氧核糖核酸,并使用基于聚合酶链反应的技术对snp进行基因分型。分析了基因型、等位基因、年龄和性别之间的关系。人口统计学和遗传学分析采用奇数比和Hardy-Weinberg平衡。结果:在DR-TB中,IFN-γ基因型/等位基因与易感性增加有显著相关性,其中胸腺嘧啶(thymine thymine, TT)基因型和T等位基因频率更高。对于IL-10,鸟嘌呤鸟嘌呤(GG)基因型和G等位基因普遍存在,表明与耐药结核病风险存在潜在关联。在DS-TB中,观察到类似的趋势,突出了对易感性的潜在遗传影响。HWE分析显示,在一些群体中存在显著差异,这表明存在遗传变异。结论:特定基因型和等位基因的流行为风险评估提供了潜在的遗传标记。与HWE的偏差表明群体特有的遗传变异。这些发现强调了遗传因素在结核病结局中的重要性,并提倡针对不同人群采取有针对性的干预措施。
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来源期刊
CiteScore
2.20
自引率
25.00%
发文量
62
审稿时长
7 weeks
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