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Published on: March 21, 2013
Circulating Autoantibodies Against Vasoactive Biomarkers Related to Orthostatic Intolerance in Long COVID Patients
Emilie Han1, Katrin Müller-Zlabinger1, Ena Hasimbegovic1
1Division of Cardiology, Department of Internal Medicine II, Medical University of Vienna, 1090 Vienna, Austria.
Insights
Elevated autoantibodies against the endothelin type A receptor (ETAR) are linked to long COVID and impact daily activities. This finding suggests a potential mechanism for long COVID symptoms.
Area of Science:
- Cardiovascular Research
- Immunology
- Infectious Diseases
Background:
- Long COVID is associated with endothelial dysfunction and orthostatic intolerance.
- Autoantibodies against vasoactive peptides are a proposed mechanism for these symptoms.
Purpose of the Study:
- To investigate autoantibody levels in long COVID patients with and without orthostatic intolerance.
- To explore the correlation between autoantibodies, routine lab parameters, and quality of life.
Main Methods:
- Case-control study with 100 long COVID patients and 60 controls.
- Enzyme-linked immunosorbent assay (ELISA) measured autoantibodies against ETAR, Beta-2 AR, Ang1-7, and others.
- Quality of life assessed using EQ-5D questionnaires.
Main Results:
- Significantly higher ETAR autoantibody concentrations in long COVID, asymptomatic, and vaccinated groups compared to healthy controls.
- A trend of higher Beta-2 AR and Ang1-7 levels in long COVID patients, not linked to orthostatic intolerance.
- ETAR autoantibody levels positively correlated with reduced ability to perform usual activities.
Conclusions:
- Elevated ETAR autoantibodies may play a role in the pathophysiology of long COVID.
- ETAR autoantibodies are associated with impaired quality of life in long COVID patients.
Abstract:
Endothelial dysfunction mediated by elevated levels of autoantibodies against vasoactive peptides occurring after COVID-19 infection is proposed as a possible pathomechanism for orthostatic intolerance in long COVID patients. This case-control study comprised 100 long COVID patients from our prospective POSTCOV registry and three control groups, each consisting of 20 individuals (Asymptomatic post-COVID group; Healthy group = pan-negative for antispike protein of SARS-CoV-2; Vaccinated healthy group = no history of COVID-19 and vaccinated). Autoantibodies towards muscarinic acetylcholine receptor M3, endothelin type A receptor (ETAR), beta-2 adrenergic receptor (Beta-2 AR), angiotensin II receptor 1 and angiotensin 1-7 (Ang1-7) concentrations were measured by enzyme-linked immunosorbent assay in long COVID patients and controls. Orthostatic intolerance was defined as inappropriate sinus tachycardia, postural tachycardia, orthostatic hypotonia and other dysautonomia symptoms, such as dizziness or blurred vision (n = 38 long COVID patients). Autoantibody concentrations were compared with routine laboratory parameters and quality of life questionnaires (EQ-5D). The concentration of ETAR autoantibodies were significantly higher in long COVID, Asymptomatic and Vaccinated groups compared to the antispike protein pan-negative Healthy group. A trend towards higher plasma levels of Beta-2 AR and Ang1-7 was measured in long COVID patients, not related to presence of orthostatic intolerance. ETAR autoantibody concentration showed significant positive correlation with the EQ-5D item "Problems in performing usual activities".
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