Why the study?
ACE2 is a key receptor for SARS-CoV2 and maintains cardiovascular homeostasis, but ACE2 expressions and their modulation in healthy and disease states remained to be explored.
Does ACE2 expression differ in patients with COVID-19, cardiovascular disease, and other diseases compared to healthy subjects?
Meta-Analysis (n=7,726)
Does ACE2 expression differ in patients with COVID-19, cardiovascular disease, and other diseases compared to healthy subjects?
Answers are grounded in this paper and cite their sources.
Membrane-bound ACE2 expression is significantly elevated in patients with cardiovascular disease and viral infections, which may have implications for SARS-CoV-2 susceptibility and pathophysiology.
BACKGROUND: 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. METHOD: 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. RESULTS: 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. CONCLUSION: 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.
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Kamthe et al. (2022) conducted a meta-analysis in COVID-19, Cardiovascular diseases, Diabetes, Pulmonary diseases, Kidney disorders, Viral infections (n=7,726). Disease state (COVID-19, CVD, diabetes, etc.) vs. Healthy subjects was evaluated on Total ACE2 expression in all diseases vs. healthy subjects (SMD 0.13, 95% CI -0.02-0.29, p=0.10).
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