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捷克第一波 SARS-CoV-2 阳性幸存者中的 ACE I/D 多态性。

ACE I/D polymorphism in Czech first-wave SARS-CoV-2-positive survivors.

机构信息

Experimental Medicine Center, Institute for Clinical and Experimental Medicine, Videnska 1958/9, Prague, Czech Republic.

Institute of Health Information and Statistics of the Czech Republic, Palackeho namesti 4, Prague, Czech Republic; Institute of Biostatistics and Analyses, Faculty of Medicine, Masaryk University, Kamenice753/5, Brno, Czech Republic.

出版信息

Clin Chim Acta. 2021 Aug;519:206-209. doi: 10.1016/j.cca.2021.04.024. Epub 2021 May 3.

DOI:10.1016/j.cca.2021.04.024
PMID:33957095
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8091801/
Abstract

BACKGROUND

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) rapidly spread from China in 2019/2020 to all continents. Significant geographical and ethnic differences were described, and host genetic background seems to be important for the resistance to and mortality of COVID-19. Angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphism (rs4646994) is one of the candidates with the potential to affect infection symptoms and mortality.

METHODS

In our study, we successfully genotyped 408 SARS-CoV-2-positive COVID-19 survivors (163 asymptomatic and 245 symptomatic) and compared them with a population-based DNA bank of 2,559 subjects.

RESULTS

The frequency of ACE I/I homozygotes was significantly increased in COVID-19 patients compared with that in controls (26.2% vs. 21.2%; P = 0.02; OR [95% CI] = 1.55 [1.17-2.05]. Importantly, however, the difference was driven just by the symptomatic subjects (29.0% vs. 21.2% of the I/I homozygotes; P = 0.002; OR [95% CI] = 1.78 [1.22-2.60]). The genotype distribution of the ACE genotypes was almost identical in population controls and asymptomatic SARS-CoV-2-positive patients (P = 0.76).

CONCLUSIONS

We conclude that ACE I/D polymorphism could have the potential to predict the severity of COVID-19, with I/I homozygotes being at increased risk of symptomatic COVID-19.

摘要

背景

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)于 2019/2020 年从中国迅速传播到各大洲。描述了显著的地理和种族差异,宿主遗传背景似乎对 COVID-19 的抵抗力和死亡率很重要。血管紧张素转换酶(ACE)插入/缺失(I/D)多态性(rs4646994)是具有潜在影响感染症状和死亡率的候选者之一。

方法

在我们的研究中,我们成功地对 408 名 SARS-CoV-2 阳性 COVID-19 幸存者(163 名无症状和 245 名有症状)进行了基因分型,并将其与基于人群的 2559 名受试者的 DNA 银行进行了比较。

结果

与对照组相比,COVID-19 患者中 ACE I/I 纯合子的频率显著增加(26.2%比 21.2%;P=0.02;OR [95%CI]为 1.55 [1.17-2.05])。然而,重要的是,这种差异仅由有症状的患者驱动(29.0%比 I/I 纯合子的 21.2%;P=0.002;OR [95%CI]为 1.78 [1.22-2.60])。ACE 基因型的基因型分布在人群对照和无症状 SARS-CoV-2 阳性患者中几乎相同(P=0.76)。

结论

我们得出结论,ACE I/D 多态性可能具有预测 COVID-19 严重程度的潜力,I/I 纯合子患有症状 COVID-19 的风险增加。

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