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Ursodeoxycholic acid is associated with a reduction in SARS-CoV-2 infection and reduced severity of COVID-19 in patients with cirrhosis.
John, Binu V; Bastaich, Dustin; Webb, Gwilym; Brevini, Teresa; Moon, Andrew; Ferreira, Raphaella D; Chin, Allison M; Kaplan, David E; Taddei, Tamar H; Serper, Marina; Mahmud, Nadim; Deng, Yangyang; Chao, Hann-Hsiang; Sampaziotis, Fotios; Dahman, Bassam.
  • John BV; Division of Gastroenterology and Hepatology, Miami VA Medical System, Miami, Florida, USA.
  • Bastaich D; Division of Digestive Health and Liver Diseases, University of Miami Miller School of Medicine, Miami, Florida, USA.
  • Webb G; Department of Health Behavior and Policy, Virginia Commonwealth University, Richmond, Virginia, USA.
  • Brevini T; Cambridge Liver Unit, Cambridge University Hospital, NHS Foundation Trust, Cambridge, UK.
  • Moon A; Wellcome-MRC Cambridge Stem Cell Institute, Cambridge, UK.
  • Ferreira RD; Division of Gastroenterology and Hepatology, University of North Carolina, Chapel Hill, North Carolina, USA.
  • Chin AM; Division of Gastroenterology and Hepatology, Miami VA Medical System, Miami, Florida, USA.
  • Kaplan DE; Herbert Wertheim Florida International University, Miami, Florida, USA.
  • Taddei TH; Division of Gastroenterology and Hepatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Serper M; Section of Gastroenterology and Hepatology, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, Pennsylvania, USA.
  • Mahmud N; Section of Digestive Diseases, Yale School of Medicine, New Haven, Connecticut, USA.
  • Deng Y; Section of Gastroenterology, VA Connecticut Healthcare System, West Haven, Connecticut, USA.
  • Chao HH; Division of Gastroenterology and Hepatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Sampaziotis F; Division of Gastroenterology and Hepatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Dahman B; Department of Health Behavior and Policy, Virginia Commonwealth University, Richmond, Virginia, USA.
J Intern Med ; 293(5): 636-647, 2023 05.
Article in English | MEDLINE | ID: covidwho-2264836
ABSTRACT
BACKGROUND AND

AIMS:

Studies have demonstrated that reducing farnesoid X receptor activity with ursodeoxycholic acid (UDCA) downregulates angiotensin-converting enzyme in human lung, intestinal and cholangiocytes organoids in vitro, in human lungs and livers perfused ex situ, reducing internalization of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) into the host cell. This offers a potential novel target against coronavirus disease 2019 (COVID-19). The objective of our study was to compare the association between UDCA exposure and SARS-CoV-2 infection, as well as varying severities of COVID-19, in a large national cohort of participants with cirrhosis.

METHODS:

In this retrospective cohort study among participants with cirrhosis in the Veterans Outcomes and Costs Associated with Liver cohort, we compared participants with exposure to UDCA, with a propensity score (PS) matched group of participants without UDCA exposure, matched for clinical characteristics, and vaccination status. The outcomes included SARS-CoV-2 infection, symptomatic, at least moderate, severe, or critical COVID-19, and COVID-19-related death.

RESULTS:

We compared 1607 participants with cirrhosis who were on UDCA, with 1607 PS-matched controls. On multivariable logistic regression, UDCA exposure was associated with reduced odds of developing SARS-CoV-2 infection (adjusted odds ratio [aOR] 0.54, 95% confidence interval [CI] 0.41-0.71, p < 0.0001). Among patients who developed COVID-19, UDCA use was associated with reduced disease severity, including symptomatic COVID-19 (aOR 0.54, 95% CI 0.39-0.73, p < 0.0001), at least moderate COVID-19 (aOR 0.51, 95% CI 0.32-0.81, p = 0.005), and severe or critical COVID-19 (aOR 0.48, 95% CI 0.25-0.94, p = 0.03).

CONCLUSIONS:

In participants with cirrhosis, UDCA exposure was associated with both a decrease in SARS-CoV-2 infection, and reduction in symptomatic, at least moderate, and severe/critical COVID-19.
Subject(s)
Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Liver Cirrhosis, Biliary Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid / Vaccines Limits: Humans Language: English Journal: J Intern Med Journal subject: Internal Medicine Year: 2023 Document Type: Article Affiliation country: Joim.13630

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Liver Cirrhosis, Biliary Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid / Vaccines Limits: Humans Language: English Journal: J Intern Med Journal subject: Internal Medicine Year: 2023 Document Type: Article Affiliation country: Joim.13630