Alsayed Badr A, Mir Rashid, Mir Mohammad M, Alnour Tarig M S, Fawzy Shereen, M Ahmed Mesaik, Amle Dnyanesh
Department of Internal Medicine, Faculty of Medicine, University of Tabuk, Tabuk, 71491, Saudi Arabia.
Department of Medical Lab technology Prince Fahad Bin Sultan Chair for Biomedical Research, Faculty of Applied Medical Sciences, University of Tabuk, Tabuk, 71491, Saudi Arabia.
Curr Genomics. 2024 Feb 23;25(1):12-25. doi: 10.2174/0113892029272497240103052359.
Altered cytokine levels have been associated with poor outcomes among COVID-19 patients. TNF-α, IL-8 and IL-10 are key cytokines in COVID-19 pathogenesis, and CXCR-2 is a major chemokine receptor involved in inflammatory response. Polymorphisms in the genes of these proteins are proposed to influence disease outcomes. In this study, we aimed to find out the association of genetic polymorphisms in TNF-α, IL-8, IL-10 and CXCR-2 genes with susceptibility to and mortality of COVID-19.
The present case-control study was conducted on 230 subjects, among whom 115 were clinically diagnosed and RT-PCR-confirmed COVID-19 patients and 115 healthy control subjects. The polymorphisms in TNFα -308 G>A (rs1800629), IL-8 -251T>A (rs4073), CXCR2 +785 C>T (rs2230054) genes were detected by ARMS -PCR assay whereas for IL-10 (-1082 G>A), rs1800896 G>A allele-specific PCR assay was used and their association with COVID-19 susceptibility and mortality was estimated by multivariate analysis. The results were analyzed for risk of infection and mortality through different inheritance models.
Frequencies of TNF-α rs1800629 GA, AA, IL-8 rs4073 TA, AA, IL-10 (-1082 G>A), rs1800896 GA and GG, and CXCR2 rs2230054 CT genotypes were significantly higher in COVID-19 patients compared to the control group ( < 0.05). Furthermore, COVID-19 patients had a higher frequency of the polymorphic A allele of TNF-α, the A allele of IL-8, the G allele of IL-10, and the T allele of CXCR2. The risk of susceptibility to COVID-19 was significantly associated with TNF-α rs1800629 GA, GA+AA genotypes and the A allele, IL-8 rs4073 TA, AA genotypes and A allele, IL-10 rs1800872 GA and CC genotypes and C allele, and CXCR2 rs2230054 CT and CT+CC genotypes. TNF-α-GA and AA genotypes and A allele, IL-8 TA and AA genotypes and A allele and CXCR-2 CC and CT genotypes have significant associations with mortality risk in COVID-19 patients, while GA and GG genotypes of the IL-10 are shown to confer significant protection against mortality from COVID-19.
The findings of this study provide important insights into the COVID-19 disease and susceptibility risk. The polymorphisms in TNFα -308 G>A (rs1800629), IL-8 -251T>A (rs4073), IL-10 (-1082 G>A), rs1800896 and CXCR2 +785 C>T (rs2230054) are associated with the risk of susceptibility to COVID-19 and with mortality in COVID-19 patients. Further studies with larger sample sizes are necessary to confirm our findings.
细胞因子水平改变与COVID-19患者的不良预后相关。肿瘤坏死因子-α(TNF-α)、白细胞介素-8(IL-8)和白细胞介素-10(IL-10)是COVID-19发病机制中的关键细胞因子,而CXC趋化因子受体2(CXCR-2)是参与炎症反应的主要趋化因子受体。这些蛋白质基因的多态性被认为会影响疾病的预后。在本研究中,我们旨在探究TNF-α、IL-8、IL-10和CXCR-2基因的遗传多态性与COVID-19易感性和死亡率之间的关联。
本病例对照研究共纳入230名受试者,其中115例为临床诊断并经逆转录聚合酶链反应(RT-PCR)确诊的COVID-19患者,115例为健康对照者。采用扩增阻滞突变系统聚合酶链反应(ARMS-PCR)检测TNFα -308 G>A(rs1800629)、IL-8 -251T>A(rs4073)、CXCR2 +785 C>T(rs2230054)基因的多态性,而对于IL-10(-1082 G>A),采用等位基因特异性PCR检测rs1800896 G>A,并通过多变量分析评估它们与COVID-19易感性和死亡率的关联。通过不同的遗传模型分析结果的感染风险和死亡率。
与对照组相比,COVID-19患者中TNF-α rs1800629 GA、AA、IL-8 rs4073 TA、AA、IL-10(-1082 G>A)、rs1800896 GA和GG以及CXCR2 rs2230054 CT基因型的频率显著更高(<0.05)。此外,COVID-19患者中TNF-α多态性A等位基因、IL-8的A等位基因、IL-10的G等位基因以及CXCR2的T等位基因的频率更高。COVID-19易感性风险与TNF-α rs1800629 GA、GA+AA基因型和A等位基因、IL-8 rs4073 TA、AA基因型和A等位基因、IL-10 rs1800872 GA和CC基因型以及C等位基因、CXCR2 rs2230054 CT和CT+CC基因型显著相关。TNF-α -GA和AA基因型以及A等位基因、IL-8 TA和AA基因型以及A等位基因和CXCR-2 CC和CT基因型与COVID-19患者的死亡风险显著相关,而IL-10的GA和GG基因型显示出对COVID-19死亡具有显著的保护作用。
本研究结果为COVID-19疾病及其易感性风险提供了重要见解。TNFα -308 G>A(rs1800629)、IL-8 -251T>A(rs4073)、IL-10(-1082 G>A)、rs1800896和CXCR2 +785 C>T(rs2230054)的多态性与COVID-19易感性风险以及COVID-19患者的死亡率相关。需要进一步开展更大样本量的研究来证实我们的发现。