Department of Pharmacology, STES's, Smt. Kashibai Navale College of Pharmacy, Savitribai Phule Pune University, Pune, India.
Eur J Clin Invest. 2023 Jan;53(1):e13891. doi: 10.1111/eci.13891. Epub 2022 Oct 25.
Angiotensin-converting enzyme 2 (ACE2) expressions and its modulation are of great interest as being a key receptor for severe acute respiratory syndrome coronavirus 2 (SARS-CoV2) and the protective arm of the rennin-angiotensin axis, maintaining cardiovascular homeostasis. However, ACE2 expressions and their modulation in the healthy and disease background are yet to be explored.
We performed a meta-analysis, extracting the data for ACE2 expression in human subjects with various diseases, including SARS-CoV2 infection without or with co-morbidity. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines were followed. Out of 203 studies, 39 met the inclusion criteria with SARS-CoV2 patients without co-morbidity, SARS-CoV2 patients with co-morbidity, cardiovascular (CVD) patients, diabetes patients, kidney disorders patients, pulmonary disease patients, and other viral infections patients.
Angiotensin-converting enzyme 2 expression was significantly increased in all diseases. There was an elevated level of ACE2, especially membrane-bound ACE2, in COVID-19 patients compared to healthy controls. A statistically significant increase in ACE2 expression was observed in CVD patients and patients with other viral diseases compared to healthy subjects. Moreover, subgroup analysis of ACE2 expression as soluble and membrane-bound ACE2 revealed a remarkable increase in membrane-bound ACE2 in CVD patients, patients with viral infection compared to soluble ACE2 and pooled standard mean difference (SMD) with the random-effects model was 0.37 and 2.23 respectively.
It was observed that utilizing the ACE2 by SARS-CoV2 for its entry and its consequence leads to several complications. So there is a need to investigate the underlying mechanism along with novel therapeutic strategies.
血管紧张素转换酶 2(ACE2)的表达及其调节是研究的热点,因为它是严重急性呼吸综合征冠状病毒 2(SARS-CoV2)的关键受体,也是肾素-血管紧张素轴的保护机制,维持心血管稳态。然而,在健康和疾病背景下,ACE2 的表达及其调节仍有待探索。
我们进行了一项荟萃分析,提取了人类各种疾病中 ACE2 表达的数据,包括 SARS-CoV2 感染无合并症或合并症的患者。我们遵循了系统评价和荟萃分析的首选报告项目(PRISMA)指南。在 203 项研究中,有 39 项符合纳入标准,包括无合并症的 SARS-CoV2 患者、有合并症的 SARS-CoV2 患者、心血管疾病(CVD)患者、糖尿病患者、肾脏疾病患者、肺部疾病患者和其他病毒感染患者。
ACE2 的表达在所有疾病中均显著增加。与健康对照组相比,COVID-19 患者的 ACE2 水平,尤其是膜结合 ACE2 水平升高。与健康受试者相比,CVD 患者和其他病毒疾病患者的 ACE2 表达水平显著升高。此外,对 ACE2 表达作为可溶性和膜结合 ACE2 的亚组分析显示,CVD 患者和病毒感染患者的膜结合 ACE2 显著增加,与可溶性 ACE2 相比,合并标准均数差(SMD)的随机效应模型分别为 0.37 和 2.23。
观察到 SARS-CoV2 利用 ACE2 进入细胞及其后果导致了多种并发症。因此,有必要研究潜在的机制以及新的治疗策略。