Depertmant of Infection Diseases and Clinical Microbiology, Health Sciences University Erzurum Regional Education and Research Hospital, Turkey.
Department of Pulmonary Diseases, Ataturk University School of Medicine, Turkey.
Jpn J Infect Dis. 2021 Nov 22;74(6):543-548. doi: 10.7883/yoken.JJID.2021.046. Epub 2021 Apr 30.
Severe acute respiratory syndrome coronavirus 2 has infected over 100 million people since it appeared in Wuhan, China, just one year ago. This study aimed to evaluate the relationship between interleukin-6 (IL-6) gene polymorphisms -174G/C and -597G/A and coronavirus disease 2019 (COVID-19) course. The study included 70 patients aged 18-45 years who were diagnosed with COVID-19 in Turkey between March and November 2020 and hospitalized in our hospital. Of these, 40 patients required intensive care admission due to macrophage activation syndrome (MAS), and 30 patients did not develop MAS or acute respiratory distress syndrome. The frequencies of the IL-6-174G/C and -597G/A polymorphisms were determined. There were significant differences between the groups in terms of the -174G/C allele and genotype frequency according to the Hardy-Weinberg equilibrium (χ = 10.029, df = 1, P = 0.002 and χ = 9.998, df = 1, P = 0.002, respectively). The frequency of the GG genotype was significantly higher in the MAS group than in the non-MAS group (P = 0.002). The G allele was also significantly more frequent in the MAS group than in the non-MAS group (P = 0.032). Analysis of the -174G/C polymorphism in patients with MAS showed that the G allele may be a risk factor for increased serum IL-6 levels and progression to MAS.
自一年前在中国武汉出现以来,严重急性呼吸综合征冠状病毒 2 已感染超过 1 亿人。本研究旨在评估白细胞介素-6 (IL-6) 基因多态性-174G/C 和-597G/A 与 2019 年冠状病毒病 (COVID-19) 病程之间的关系。该研究包括 2020 年 3 月至 11 月在土耳其被诊断患有 COVID-19 并在我院住院的 70 名年龄在 18-45 岁的患者。其中,40 名患者因巨噬细胞活化综合征 (MAS) 需要重症监护入院,30 名患者未发生 MAS 或急性呼吸窘迫综合征。确定了 IL-6-174G/C 和-597G/A 多态性的频率。根据 Hardy-Weinberg 平衡,两组在-174G/C 等位基因和基因型频率方面存在显著差异(χ=10.029,df=1,P=0.002 和 χ=9.998,df=1,P=0.002)。MAS 组 GG 基因型的频率明显高于非 MAS 组(P=0.002)。MAS 组的 G 等位基因也明显多于非 MAS 组(P=0.032)。对 MAS 患者-174G/C 多态性的分析表明,G 等位基因可能是血清 IL-6 水平升高和进展为 MAS 的危险因素。