Distribution of Genotypes for the rs12979860 Polymorphism of the IFNL Gene among Children with COVID-19 in Ukraine

Pub Date : 2023-12-04 DOI:10.3103/s0095452723060038
T. A. Harashchenko, T. R. Umanets, T. M. Kaminska, O. V. Gorodna, D. S. Krasnienkov, Yu. G. Antypkin, L. A. Livshits
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Abstract

The coronavirus disease (COVID-19), which is caused by a severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), was for the first time detected in December 2019. At the beginning of the pandemic, it was believed that children are less susceptible to COVID-19 compared to adults, but further studies demonstrated that children are also susceptible to infection with the SARS-CoV-2 virus. In recent years, appeared studies about the role of genetic factors in the course of COVID-19. This fact suggests a possible existence of hereditary predisposition of individuals to infection with the SARS-CoV-2 virus. Recently, data was obtained that certain genetic polymorphisms (particularly, different genotypes for the polymorphic variant rs12979860 of the IFNL gene) can act as predictors of the severe course of respiratory infections in children (particularly, COVID-19). The aim of this work was to study the peculiarities of the genotype distribution for the IFNL gene rs12979860 polymorphism in a cohort of children who suffered from COVID-19 as well as to estimate the association of this polymorphism with a risk of infection with the SARS-CoV-2 virus, the development of pneumonia during the coronavirus disease, and the course of this disease among children with recurrent respiratory infections (RRI). For this purpose, genotyping for the IFNL gene rs12979860 locus polymorphism was carried out in the studied group of 70 children who had a laboratory-confirmed COVID-19. According to the results of the study, it was established that the C allele was more common in children with RRI as compared with those with episodic viral infections (p < 0.05, OR 3.2; CI 1.52–6.71); therefore, this variant can be considered as a risk allele for more frequent viral infections. In addition, the C allele predominated in the subgroup of children with pneumonia (p < 0.05, OR 2.36; CI 1.19–4.68), indicating that the C allele can be considered a risk allele for a more severe course of COVID-19 due to pneumonia. The results obtained suggest that the C allele can act as a predictive marker of the risk of developing pneumonia in children with COVID-19. In addition, the carriage of the C allele is associated with cases of RRI among children.

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乌克兰新冠肺炎儿童IFNL基因rs12979860多态性基因型分布
由严重急性呼吸系统综合征冠状病毒-2 (SARS-CoV-2)引起的冠状病毒病(COVID-19)于2019年12月首次被发现。在大流行开始时,人们认为与成人相比,儿童对COVID-19的易感程度较低,但进一步的研究表明,儿童也容易感染SARS-CoV-2病毒。近年来,出现了遗传因素在COVID-19发病过程中的作用的研究。这一事实表明,个体可能存在感染SARS-CoV-2病毒的遗传倾向。最近,有数据表明,某些遗传多态性(特别是IFNL基因多态性变异rs12979860的不同基因型)可以作为儿童呼吸道感染(特别是COVID-19)严重病程的预测因子。这项工作的目的是研究一组患有COVID-19的儿童中IFNL基因rs12979860多态性的基因型分布的特殊性,并估计这种多态性与感染SARS-CoV-2病毒的风险、冠状病毒疾病期间肺炎的发展以及复发性呼吸道感染(RRI)儿童的病程之间的关系。为此,对70例实验室确诊的COVID-19患儿研究组进行了IFNL基因rs12979860位点多态性的基因分型。根据研究结果,可以确定C等位基因在RRI患儿中比在发作性病毒感染患儿中更常见(p <0.05,或3.2;可信区间1.52 - -6.71);因此,这种变异可以被认为是更频繁的病毒感染的风险等位基因。此外,C等位基因在肺炎儿童亚组中占主导地位(p <0.05,或2.36;CI 1.19-4.68),表明C等位基因可被认为是肺炎引起的COVID-19更严重病程的风险等位基因。这些结果表明,C等位基因可以作为COVID-19儿童发生肺炎风险的预测标志物。此外,携带C等位基因与儿童RRI病例有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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