Angiotensin-Converting Enzyme-2 (ACE-2) with Interferon-Induced Transmembrane Protein-3 (IFITM-3) Genetic Variants and Interleukin-6 as Severity and Risk Predictors among COVID-19 Egyptian Population

IF 2.8 Q3 MICROBIOLOGY
Amal F. Makled, Sahar A. M. Ali, S. S. Eldahdouh, Asmaa S. Sleem, Maha M. Eldahshan, Yara Elsaadawy, Samar S. Salman, Asmaa Mohammed Elbrolosy
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Abstract

Introduction. The host genetic background is a crucial factor that underlies the interindividual variability of COVID-19 fatality and outcomes. Angiotensin-converting enzyme-2 (ACE-2) and interferon-induced transmembrane protein-3 (IFITM-3) have a key role in viral cell entrance and priming. The evoked immune response will also provide a predictive prognosis for COVID-19 infection. This study aimed to explore the association between ACE-2 and IFITM-3 genotypes and their corresponding allele frequencies with disease severity indices in the Egyptian COVID-19 population. The serum level of interleukin-6, as a biomarker of hyperinflammatory response, and cytokine storm, was correlated with disease progression, single nucleotide polymorphisms (SNPs) of the selected receptors, and treatment response. Methodology. We enrolled 900 COVID-19-confirmed cases and 100 healthy controls. Genomic DNA was extracted from 200 subjects (160 patients selected based on clinical and laboratory data and 40 healthy controls). The ACE-2 rs2285666 and IFITM-3 rs12252 SNPs were genotyped using the TaqMan probe allelic discrimination assay, and the serum IL-6 level was determined by ELISA. Logistic regression analysis was applied to analyze the association between ACE-2 and IFITM-3 genetic variants, IL-6 profile, and COVID-19 severity. Results. The identified genotypes and their alleles were significantly correlated with COVID-19 clinical deterioration as follows: ACE2 rs2285666 CT + TT, odds ratio (95% confidence interval): 12.136 (2.784–52.896) and IFITM-3 rs12252 AG + GG: 17.276 (3.673–81.249), both p<0.001. Compared to the controls, the heterozygous and mutant genotypes for both SNPs were considerable risk factors for increased susceptibility to COVID-19. IL-6 levels were significantly correlated with disease progression (p<0.001). Conclusion. ACE-2 and IFITM-3 genetic variants are potential predictors of COVID-19 severity, critical outcomes, and post-COVID-19 complications. Together, these SNPs and serum IL-6 levels explain a large proportion of the variability in the severity of COVID-19 infection and its consequences among Egyptian subjects.
血管紧张素转换酶-2 (ACE-2)与干扰素诱导跨膜蛋白-3 (IFITM-3)基因变异和白细胞介素-6作为 COVID-19 埃及人群的严重性和风险预测因子
简介宿主的遗传背景是导致 COVID-19 死亡率和结果个体间差异的关键因素。血管紧张素转换酶-2(ACE-2)和干扰素诱导跨膜蛋白-3(IFITM-3)在病毒细胞进入和启动过程中起着关键作用。诱发的免疫反应还可预测 COVID-19 感染的预后。本研究旨在探讨埃及 COVID-19 群体中 ACE-2 和 IFITM-3 基因型及其相应等位基因频率与疾病严重程度指数之间的关联。作为高炎症反应和细胞因子风暴生物标志物的血清白细胞介素-6水平与疾病进展、所选受体的单核苷酸多态性(SNPs)和治疗反应相关。研究方法我们招募了 900 名 COVID-19 确诊病例和 100 名健康对照者。从 200 名受试者(根据临床和实验室数据选出 160 名患者和 40 名健康对照者)中提取基因组 DNA。使用 TaqMan 探针等位基因鉴别测定法对 ACE-2 rs2285666 和 IFITM-3 rs12252 SNP 进行基因分型,并通过 ELISA 测定血清 IL-6 水平。应用逻辑回归分析法分析了ACE-2和IFITM-3基因变异、IL-6特征和COVID-19严重程度之间的关联。结果已确定的基因型及其等位基因与 COVID-19 临床恶化有如下显著相关性:ACE2 rs2285666 CT + TT,几率比(95% 置信区间):12.136(2.784-52.896)和 IFITM-3 rs12252 AG + GG:17.276(3.673-81.249),均 p<0.001。与对照组相比,这两个 SNP 的杂合基因型和突变基因型是 COVID-19 易感性增加的重要危险因素。IL-6水平与疾病进展明显相关(p<0.001)。结论ACE-2 和 IFITM-3 基因变异是 COVID-19 严重程度、危重结果和 COVID-19 后并发症的潜在预测因素。这些 SNPs 和血清 IL-6 水平共同解释了埃及受试者 COVID-19 感染严重程度及其后果的大部分差异。
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来源期刊
CiteScore
7.90
自引率
0.00%
发文量
57
审稿时长
13 weeks
期刊介绍: International Journal of Microbiology is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies on microorganisms and their interaction with hosts and the environment. The journal covers all microbes, including bacteria, fungi, viruses, archaea, and protozoa. Basic science will be considered, as well as medical and applied research.
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