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The Comparative Immunological Characteristics of SARS-CoV, MERS-CoV, and SARS-CoV-2 Coronavirus Infections.SARS-CoV、MERS-CoV 和 SARS-CoV-2 冠状病毒感染的比较免疫学特征。
Front Immunol. 2020 Aug 14;11:2033. doi: 10.3389/fimmu.2020.02033. eCollection 2020.
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Single-Cell RNA Expression Profiling of ACE2, the Receptor of SARS-CoV-2.新型冠状病毒(SARS-CoV-2)受体ACE2的单细胞RNA表达谱分析
Am J Respir Crit Care Med. 2020 Sep 1;202(5):756-759. doi: 10.1164/rccm.202001-0179LE.
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Definition and Risks of Cytokine Release Syndrome in 11 Critically Ill COVID-19 Patients With Pneumonia: Analysis of Disease Characteristics.新冠肺炎肺炎 11 例危重症患者细胞因子释放综合征的定义和风险:疾病特征分析。
J Infect Dis. 2020 Oct 1;222(9):1444-1451. doi: 10.1093/infdis/jiaa387.
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Older age and comorbidity are independent mortality predictors in a large cohort of 1305 COVID-19 patients in Michigan, United States.在美国密歇根州的一个大型 1305 名 COVID-19 患者队列中,年龄较大和合并症是独立的死亡预测因素。
J Intern Med. 2020 Oct;288(4):469-476. doi: 10.1111/joim.13119. Epub 2020 Jun 22.
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Cardiovascular Disease, Drug Therapy, and Mortality in Covid-19.心血管疾病、药物治疗与新冠病毒感染相关死亡率
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The pivotal link between ACE2 deficiency and SARS-CoV-2 infection.ACE2 缺乏与 SARS-CoV-2 感染之间的关键联系。
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Risk factors of critical & mortal COVID-19 cases: A systematic literature review and meta-analysis.危重症和死亡 COVID-19 病例的风险因素:系统文献回顾和荟萃分析。
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Presenting Characteristics, Comorbidities, and Outcomes Among 5700 Patients Hospitalized With COVID-19 in the New York City Area.在纽约市地区,5700 名因 COVID-19 住院的患者的特征、合并症和结局。
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评估 COVID-19 患者血清 ACE 活性及其与临床特征和疾病严重程度的关系。

The assessment of serum ACE activity in COVID-19 and its association with clinical features and severity of the disease.

机构信息

Faculty of Medicine, Rheumatology Department, Gazi University Hospital, Ankara, Turkey.

Faculty of Medicine, Biochemistry Department, Gazi University Hospital, Ankara, Turkey.

出版信息

Scand J Clin Lab Invest. 2021 Apr;81(2):160-165. doi: 10.1080/00365513.2021.1871641. Epub 2021 Jan 21.

DOI:10.1080/00365513.2021.1871641
PMID:33474994
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7832453/
Abstract

Angiotensin-converting enzyme (ACE)/Angiotensin (Ang) II pathway has crucial regulatory effects on circulatory hemostasis and immune responses. This pathway has a major role in the development of acute lung injury and acute respiratory distress syndrome (ARDS), which is a devastating complication of SARS-CoV-2 infection. The aim of this study is to investigate the serum ACE activity and its correlation with clinical features and the disease severity in patients with COVID-19. Patients with confirmed COVID-19 by detecting SARS-CoV-2 nucleic acid RT-PCR were included in the study. Demographic data, clinical features, laboratory and radiologic investigations were recorded. Patients were classified by disease severity; asymptomatic, mild, and severe pneumonia. The serum ACE activity was evaluated with an autoanalyzer based on a spectrophotometric method. Fifty-five patients (50.9% female) and 18 healthy subjects (33.3 % female) were enrolled in the study. The median age of patients was 40 years, ranging from 22 to 81 years. Eighteen healthy subjects were served as the control group. The baseline characteristics were comparable between groups. The median serum ACE activity of patients and controls (38.00 [IQR 21] U/L and 32.00 [IQR 24] U/L, respectively) and of between patients grouped by disease severity (38.5 [IQR 19], 36 [IQR 25], and 38 [IQR 22] U/L, asymptomatic, mild and severe pneumonia group, respectively) were similar. There was no correlation between the serum ACE activity and conventional inflammatory markers. In this study, we did not find an association between serum ACE activity and COVID-19 and serum ACE activity on admission did not reflect disease severity.

摘要

血管紧张素转换酶(ACE)/血管紧张素(Ang)II 途径对循环止血和免疫反应具有重要的调节作用。该途径在急性肺损伤和急性呼吸窘迫综合征(ARDS)的发展中起主要作用,这是 SARS-CoV-2 感染的一种破坏性并发症。本研究旨在探讨 COVID-19 患者血清 ACE 活性及其与临床特征和疾病严重程度的相关性。研究纳入了通过检测 SARS-CoV-2 核酸 RT-PCR 确诊为 COVID-19 的患者。记录了人口统计学数据、临床特征、实验室和影像学检查。根据疾病严重程度将患者分为无症状、轻症和重症肺炎。采用基于分光光度法的自动分析仪评估血清 ACE 活性。研究纳入了 55 名患者(50.9%为女性)和 18 名健康对照者(33.3%为女性)。患者的中位年龄为 40 岁,范围为 22 至 81 岁。18 名健康对照者作为对照组。两组的基线特征无差异。患者和对照组的中位血清 ACE 活性分别为 38.00 [IQR 21] U/L 和 32.00 [IQR 24] U/L,不同疾病严重程度患者的血清 ACE 活性分别为 38.5 [IQR 19]、36 [IQR 25]和 38 [IQR 22] U/L,无统计学差异。血清 ACE 活性与常规炎症标志物之间无相关性。在本研究中,我们未发现血清 ACE 活性与 COVID-19 之间存在关联,入院时的血清 ACE 活性也不能反映疾病的严重程度。