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Angiotensin II receptor I auto-antibodies following SARS-CoV-2 infection.
Jiang, Yonghou; Duffy, Fergal; Hadlock, Jennifer; Raappana, Andrew; Styrchak, Sheila; Beck, Ingrid; Mast, Fred D; Miller, Leslie R; Chour, William; Houck, John; Armistead, Blair; Duvvuri, Venkata R; Yeung, Winnie; Haglund, Micaela; Wallner, Jackson; Wallick, Julie A; Hardy, Samantha; Oldroyd, Alyssa; Ko, Daisy; Gervassi, Ana; Murray, Kim M; Kaplan, Henry; Aitchison, John D; Heath, James R; Sather, D Noah; Goldman, Jason D; Frenkel, Lisa; Harrington, Whitney E.
Affiliation
  • Jiang Y; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Duffy F; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Hadlock J; Institute for Systems Biology, Seattle, Washington, United States of America.
  • Raappana A; Providence St. Joseph Health, Renton, Washington, United States of America.
  • Styrchak S; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Beck I; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Mast FD; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Miller LR; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Chour W; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Houck J; Institute for Systems Biology, Seattle, Washington, United States of America.
  • Armistead B; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, California, United States of America.
  • Duvvuri VR; Keck School of Medicine, University of Southern California, Los Angeles, California, United States of America.
  • Yeung W; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Haglund M; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Wallner J; Institute for Systems Biology, Seattle, Washington, United States of America.
  • Wallick JA; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Hardy S; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Oldroyd A; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Ko D; Providence St. Joseph Health, Renton, Washington, United States of America.
  • Gervassi A; Swedish Center for Research and Innovation, Swedish Medical Center, Seattle, Washington, United States of America.
  • Murray KM; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Kaplan H; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Aitchison JD; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Heath JR; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Sather DN; Institute for Systems Biology, Seattle, Washington, United States of America.
  • Goldman JD; Swedish Cancer Institute, Swedish Medical Center, Seattle, Washington, United States of America.
  • Frenkel L; Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, United States of America.
  • Harrington WE; Department of Pediatrics, University of Washington, Seattle, Washington, United States of America.
PLoS One ; 16(11): e0259902, 2021.
Article in En | MEDLINE | ID: mdl-34788328
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: COVID-19 Type of study: Risk_factors_studies Limits: Adult / Humans / Male / Middle aged Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: COVID-19 Type of study: Risk_factors_studies Limits: Adult / Humans / Male / Middle aged Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2021 Type: Article Affiliation country: United States