College of Medicine, University of Garmian, Kalar, Iraq.
Coronavirus Research and Identification Laboratory, University of Garmian, Kalar, Iraq.
J Clin Lab Anal. 2022 May;36(5):e24400. doi: 10.1002/jcla.24400. Epub 2022 Apr 4.
Uncovering risk factors playing roles in the severity of Coronavirus disease 2019 (Covid-19) are important for understanding pathoimmunology of the disease caused by severe acute respiratory syndrome Coronavirus 2 (SARS CoV-2). Genetic variations in innate immune genes have been found to be associated with Covid-19 infections. A single-nucleotide polymorphism (SNP) in a promoter region of tumor necrosis factor alpha (TNF-α) gene, TNF-α -308G>A, increases expression of TNF-α protein against infectious diseases leading to immune dysregulations and organ damage. This study aims to discover associations between TNF-α -308G>A SNP and Covid-19 infection. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was used for genotyping a general Kurdish population and Covid-19 patients. The homozygous mutant (AA) genotype was found to be rare in the current studied population. Interestingly, the heterozygous (GA) genotype was significantly (p value = 0.0342) higher in the Covid-19 patients than the general population. This suggests that TNF-α -308G>A SNP might be associated with Covid-19 infections. Further studies with larger sample sizes focusing on different ethnic populations are recommended.
揭示在 2019 年冠状病毒病(COVID-19)严重程度中起作用的风险因素对于了解由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起的疾病的病理免疫学非常重要。已经发现先天免疫基因中的遗传变异与 COVID-19 感染有关。肿瘤坏死因子-α(TNF-α)基因启动子区域的单核苷酸多态性(SNP)TNF-α -308G>A 增加了针对感染性疾病的 TNF-α 蛋白的表达,导致免疫失调和器官损伤。本研究旨在发现 TNF-α -308G>A SNP 与 COVID-19 感染之间的关联。聚合酶链反应-限制性片段长度多态性(PCR-RFLP)用于对库尔德族一般人群和 COVID-19 患者进行基因分型。在当前研究的人群中,纯合突变(AA)基因型很少见。有趣的是,COVID-19 患者的杂合(GA)基因型明显(p 值=0.0342)高于一般人群。这表明 TNF-α -308G>A SNP 可能与 COVID-19 感染有关。建议进行具有更大样本量并关注不同种族人群的进一步研究。