Buchynskyi Mykhailo, Oksenych Valentyn, Kamyshna Iryna, Budarna Olena, Halabitska Iryna, Petakh Pavlo, Kamyshnyi Oleksandr
Department of Microbiology, Virology, and Immunology, I. Horbachevsky Ternopil National Medical University, Ternopil, Ukraine.
Broegelmann Research Laboratory, Department of Clinical Science, University of Bergen, Bergen, Norway.
Front Genet. 2024 Sep 4;15:1460318. doi: 10.3389/fgene.2024.1460318. eCollection 2024.
This study investigated the influence of single nucleotide polymorphisms (SNPs) in genes associated with the interferon pathway (IFNAR2 rs2236757), antiviral response (OAS1 rs10774671, OAS3 rs10735079), and viral entry (ACE2 rs2074192) on COVID-19 severity and their association with nonalcoholic fatty liver disease (MAFLD). We did not observe a significant association between the investigated SNPs and COVID-19 severity. While the IFNAR2 rs2236757 A allele was correlated with higher creatinine levels upon admission and the G allele was correlated with lower band neutrophils upon discharge, these findings require further investigation. The distribution of OAS gene polymorphisms (rs10774671 and rs10735079) did not differ between MAFLD patients and non-MAFLD patients. Our study population's distribution of ACE2 rs2074192 genotypes and alleles differed from that of the European reference population. Overall, our findings suggest that these specific SNPs may not be major contributors to COVID-19 severity in our patient population, highlighting the potential role of other genetic factors and environmental influences.
本研究调查了与干扰素通路相关基因(IFNAR2 rs2236757)、抗病毒反应相关基因(OAS1 rs10774671、OAS3 rs10735079)以及病毒进入相关基因(ACE2 rs2074192)中的单核苷酸多态性(SNP)对新冠病毒疾病(COVID-19)严重程度的影响及其与非酒精性脂肪性肝病(MAFLD)的关联。我们未观察到所研究的SNP与COVID-19严重程度之间存在显著关联。虽然IFNAR2 rs2236757的A等位基因与入院时较高的肌酐水平相关,G等位基因与出院时较低的带状中性粒细胞相关,但这些发现需要进一步研究。MAFLD患者和非MAFLD患者之间OAS基因多态性(rs10774671和rs10735079)的分布没有差异。我们研究人群中ACE2 rs2074192基因型和等位基因的分布与欧洲参考人群不同。总体而言,我们的研究结果表明,这些特定的SNP可能不是我们患者群体中COVID-19严重程度的主要影响因素,这凸显了其他遗传因素和环境影响的潜在作用。