冠状病毒重症、轻症或无症状感染者ACEII基因多态性的研究

Fatemeh Arab, Mozhdeh Jafari Rad, Seyed-Alireza Esmaeili, A. Mirhosseini, Mehran Moharreri, E. Saburi
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引用次数: 2

摘要

血管紧张素转换酶2 (ACE2)是2019冠状病毒病(COVID-19)在宿主细胞中的中心受体。ACE2基因的遗传多态性可能促进COVID-19患者的心血管疾病和全身性炎症损伤。因此,遗传背景可以解释疾病易感性或严重程度的个体间差异。我们的研究旨在发现ACE2 rs4646142和rs2285666多态性与严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)易感性之间的显著关系。方法:本研究随机抽取230例样本,其中临床症状较重的患者76例,临床症状较轻的患者154例(阳性病例采用实时逆转录酶聚合酶链反应(RT-PCR)法确诊)。然后,我们提取了rs2285666和rs4646142的DNA,用TaqI和Alu1限制性内切酶的RFLP-PCR方法研究了它们的多态性。结果:研究人群男性107人,女性123人,平均(±SD)年龄为42.66±10.2岁。首先,检测IgM和IgG水平,发现两组轻、重度症状患者IgM水平显著相关,而IgG水平显著相关。同时,ACE2 rs4646142和rs2285666多态性与COVID-19严重程度无显著差异。结论:为了更好地了解人对COVID-19易感性的遗传变异,本研究旨在评估ACE2各种多态性与SARS-CoV-2感染风险的相关性。然而,没有发现统计学差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation of Polymorphisms of ACEII Gene in People With Coronavirus With Severe and Mild Symptoms or Asymptomatic
Introduction: Angiotensin-converting enzyme 2 (ACE2) is the central receptor of coronavirus disease 2019 (COVID-19) in host cells. Genetic polymorphisms in the ACE2 gene may promote cardiovascular disease and systemic inflammatory injury in a patient affected by COVID-19. Thus, the genetic background may account for the substantial inter-individual diversity in illness susceptibility or severity. Our study was conducted to find a significant relationship between ACE2 rs4646142 and rs2285666 polymorphisms and susceptibility to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Methods: In this study, we randomly selected 230 samples, including 76 patients with severe clinical symptoms and 154 patients with mild clinical symptoms (the positive case of COVID-19 was confirmed by real-time reverse transcriptase polymerase chain reaction [RT-PCR] assay). Then, we performed DNA extraction and investigated the polymorphisms of rs2285666 and rs4646142 by RFLP-PCR method with TaqI and Alu1 restriction enzymes. Results: The study population included 107 men and 123 women, and the mean (±SD) age of the participants was 42.66±10.2. First, the levels of IgM and IgG were examined, and a significant association was observed in the level of IgM between the two groups of COVID-19 patients with mild and severe symptoms, as opposed to IgG. Meanwhile, no significant difference was observed between ACE2 rs4646142 and rs2285666 polymorphisms and the severity of COVID-19. Conclusion: To better understand the genetic variations in people’s susceptibility to COVID-19, this study was designed to evaluate the association between various ACE2 polymorphisms and the infection risk of SARS-CoV-2. However, no statistical difference was discovered.
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