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Angiotensin II receptor I auto-antibodies following SARS-CoV-2 infection

Authors :
Yonghou Jiang
Fergal Duffy
Jennifer Hadlock
Andrew Raappana
Sheila Styrchak
Ingrid Beck
Fred D. Mast
Leslie R. Miller
William Chour
John Houck
Blair Armistead
Venkata R. Duvvuri
Winnie Yeung
Micaela Haglund
Jackson Wallner
Julie A. Wallick
Samantha Hardy
Alyssa Oldroyd
Daisy Ko
Ana Gervassi
Kim M. Murray
Henry Kaplan
John D. Aitchison
James R. Heath
D. Noah Sather
Jason D. Goldman
Lisa Frenkel
Whitney E. Harrington
Source :
PLoS ONE, Vol 16, Iss 11 (2021)
Publication Year :
2021
Publisher :
Public Library of Science (PLoS), 2021.

Abstract

Background Coronavirus disease 2019 (COVID-19) is associated with endothelial activation and coagulopathy, which may be related to pre-existing or infection-induced pro-thrombotic autoantibodies such as those targeting angiotensin II type I receptor (AT1R-Ab). Methods We compared prevalence and levels of AT1R-Ab in COVID-19 cases with mild or severe disease to age and sex matched negative controls utilizing multivariate logistic and quantile regression adjusted for comorbidities including hypertension, diabetes, and heart disease. Results There were trends toward increased prevalence (50% vs. 33%, p = 0.1) and level of AT1R-Ab (median 9.8 vs. 6.1 U/mL, p = 0.06) in all cases versus controls. When considered by COVID-19 disease severity, there was a trend toward increased prevalence of AT1R-Ab (55% vs. 31%, p = 0.07), as well as significantly higher AT1R-Ab levels (median 10.7 vs. 5.9 U/mL, p = 0.03) amongst individuals with mild COVID-19 versus matched controls. In contrast, the prevalence (42% vs. 37%, p = 0.9) and level (both medians 6.7 U/mL, p = 0.9) of AT1R-Ab amongst those with severe COVID-19 did not differ from matched controls. Conclusions These findings support an association between COVID-19 and AT1R-Ab, emphasizing that vascular pathology may be present in individuals with mild COVID-19 as well as those with severe disease.

Subjects

Subjects :
Medicine
Science

Details

Language :
English
ISSN :
19326203
Volume :
16
Issue :
11
Database :
Directory of Open Access Journals
Journal :
PLoS ONE
Publication Type :
Academic Journal
Accession number :
edsdoj.573774925a43b6bf26a92fa1b1734f
Document Type :
article