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Published on: June 7, 2016
The Renin-Angiotensin System in COVID-19: Can Long COVID Be Predicted?
Simone König1, Richard Vollenberg2, Phil-Robin Tepasse2
1IZKF Core Unit Proteomics, University of Münster, 48149 Münster, Germany.
Insights
Long COVID may be identified by measuring bradykinin (BK) serum degradation. This assay could detect dysregulation in the renin-angiotensin system (RAS) and kallikrein-kinin system (KKS), often missed by standard tests.
Area of Science:
- Biochemistry
- Immunology
- Pathophysiology
Background:
- Hypertension and cardiovascular disease increase severe COVID-19 risk.
- The renin-angiotensin system (RAS) and kallikrein-kinin system (KKS) are implicated in COVID-19 pathophysiology.
- Components of RAS and KKS are targets for COVID-19 research and treatment.
Purpose of the Study:
- To investigate if bradykinin (BK) serum degradation indicates Long COVID.
- To explore the link between BK degradation, RAS, and KKS dysregulation in Long COVID patients.
Main Methods:
- Analysis of carboxypeptidase N (CPN) activity and angiotensin-converting enzyme (ACE) activity in patient sera.
- Use of labeled bradykinin (BK) as a reporter peptide to measure serum degradation.
- Supplementation with mass-spectrometry-based serum proteomic analysis.
Main Results:
- Significantly reduced CPN activity and excessive ACE activity were observed in hospitalized and some convalescent COVID-19 patients.
- BK serum degradation products did not normalize in nearly half of patients during convalescence, suggesting potential RAS dysregulation.
- Standard diagnostic tests for Long COVID often yield normal results.
Conclusions:
- BK serum degradation may serve as a biomarker for Long COVID.
- Measuring ACE, angiotensin II, or using a BK degradation assay could help identify Long COVID candidates.
- Further clinical studies are necessary to validate these findings.
Abstract:
(1) Background: Co-morbidities such as hypertension and cardiovascular disease are major risk factors for severe COVID-19. The renin-angiotensin system (RAS) is critically involved in their pathophysiology and is counter-balanced by both angiotensin-converting enzyme 2 (ACE2), the functional receptor of SARS-CoV-2, and the kallikrein-kinin system (KKS). Considerable research interest with respect to COVID-19 treatment is currently being directed towards the components of these systems. In earlier studies, we noticed significantly reduced carboxypeptidase N (CPN, KKS member) activity and excessive angiotensin-converting enzyme (ACE, RAS member) activity in the sera of both hospitalized COVID-19 patients and a subgroup of convalescent patients. The data had been obtained using labeled bradykinin (BK) as a reporter peptide, which is a target of both CPN and ACE. The data were supplemented with mass-spectrometry-based serum proteomic analysis. Here, we hypothesize that the degree of BK serum degradation could be indicative of Long COVID. (2) Review and Discussion: The recent literature is briefly reviewed. The fact that the levels of the BK serum degradation products did not reach normal concentrations in almost half of the patients during convalescences could have been partially due to a dysregulated RAS. (3) Conclusions: Standard tests for routine patient care in Long COVID come often back normal. We suggest that the measurement of selected members of the RAS such as ACE and angiotensin II or the use of our BK degradation assay could identify Long COVID candidates. Clinical studies are required to test this hypothesis.
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