Clinical effects of ursodeoxycholic acid in COVID-19 infection: a systematic review and dose–response meta-analysis
et al., Frontiers in Pharmacology, doi:10.3389/fphar.2026.1719144, PROSPERO CRD420251019195, Mar 2026
Systematic review and meta-analysis of 15 studies with 716,310 participants showing lower COVID-19 infection risk, severe infection risk, and ventilator use with ursodeoxycholic acid (UDCA) treatment. A dose-response relationship was observed, with increasing UDCA doses associated with progressively lower infection risk. No significant differences were found for mortality, hospitalization, ICU admission, or recovery time.
2 meta-analyses show significant improvements with ursodeoxycholic acid for mechanical ventilation1,
severity1,2, and
cases1.
Currently there are 21 ursodeoxycholic acid for COVID-19 studies, showing 7% lower mortality [-27‑33%], 6% lower ventilation [-293‑78%], 27% lower ICU admission [-52‑65%], 10% lower hospitalization [-7‑24%], and 17% fewer cases [11‑23%].
Song et al., 31 Mar 2026, China, peer-reviewed, 9 authors, trial PROSPERO CRD420251019195.
Contact: sungryul.shim@gmail.com, kchuh2020@hanmail.net.
Abstract:
OPEN ACCESS
EDITED BY Ranjan K. Mohapatra, Government College of Engineering, Keonjhar, India
REVIEWED BY
Bijaya Kumar Padhi, Post Graduate Institute of Medical Education and Research (PGIMER), India Kokouvi Kassegne,
Shanghai Jiao Tong University, China sungryul.shim@gmail.com
*CORRESPONDENCE Sung Ryul Shim, Kyu Chan Huh, kchuh2020@hanmail.net
RECEIVED 03 November 2025 REVISED 05 February 2026 ACCEPTED 20 February 2026 PUBLISHED 01 April 2026
CITATION
Song JH, Shim SR, Shin J, Choe WH, Park J, Lee TH, Kang S, Rhee TG and Huh KC (2026) Clinical effects of ursodeoxycholic acid in COVID-19 infection: a systematic review and dose-response meta-analysis. Front. Pharmacol. 17:1719144. doi: 10.3389/fphar.2026.1719144
COPYRIGHT
© 2026 Song, Shim, Shin, Choe, Park, Lee, Kang, Rhee and Huh. This is an openaccess article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
[Clinical effects of ursodeoxycholic acid in COVID-19 infection: a systematic review and dose-response meta-analysis](https://www.frontiersin.org/articles/10.3389/fphar.2026.1719144/full)
Joo Hye Song 1 , Sung Ryul Shim 2,3 *, Jieun Shin 2,3 , Won Hyeok Choe 1 , Jiho Park 4 , Tae Hee Lee 5 , Seonghui Kang 6 , Taeho Greg Rhee 7,8 and Kyu Chan Huh 5 *
1 Division of Gastroenterology, Department of Internal Medicine, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Republic of Korea, 2 Department of Biomedical Informatics, College of Medicine, Konyang University, Daejeon, Republic of Korea, 3 Evidence Based Research Center, Konyang University Hospital, Daejeon, Republic of Korea, 4 Division of Infectious Diseases, Department of Internal Medicine, Konkuk University of Medical Center, Konkuk University School of Medicine, Seoul, Republic of Korea, 5 Division of Gastroenterology, Department of Internal Medicine, Konyang University College of Medicine, Daejeon, Republic of Korea, 6 Division of Infectious Diseases, Department of Internal Medicine, Konyang University College of Medicine, Daejeon, Republic of Korea, 7 Department of Psychiatry, Yale University School of Medicine, New Haven, CT, United States, 8 Department of Public Health Sciences, University of Connecticut School of Medicine, Farmington, CT, United States
Objectives: Previous studies have shown that ursodeoxycholic acid (UDCA) reduces COVID-19 infection by inhibiting farnesoid X receptor activity, a direct regulator of ACE2. Even though UDCA, an easily accessible medication with few side effects, could be considered for administration to prevent infection and relieve symptoms for COVID-19 infection, there are limited supporting studies with a high-level of evidence and recommendations for the exact dosage of UDCA. We conducted a systematic review and dose-response meta-analysis to evaluate the clinical effect of UDCA in COVID-19 infection.
Methods: Studies were identified through a literature search: PubMed, Embase, and Cochrane from inception to March 2025. We included research related to COVID-19 infection and UDCA. Primary outcomes were COVID-19 infection rate, mortality rate, COVID-19..
DOI record:
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"abstract": "<jats:sec>\n <jats:title>Objectives</jats:title>\n <jats:p>Previous studies have shown that ursodeoxycholic acid (UDCA) reduces COVID-19 infection by inhibiting farnesoid X receptor activity, a direct regulator of ACE2. Even though UDCA, an easily accessible medication with few side effects, could be considered for administration to prevent infection and relieve symptoms for COVID-19 infection, there are limited supporting studies with a high-level of evidence and recommendations for the exact dosage of UDCA. We conducted a systematic review and dose–response meta-analysis to evaluate the clinical effect of UDCA in COVID-19 infection.</jats:p>\n </jats:sec>\n <jats:sec>\n <jats:title>Methods</jats:title>\n <jats:p>Studies were identified through a literature search: PubMed, Embase, and Cochrane from inception to March 2025. We included research related to COVID-19 infection and UDCA. Primary outcomes were COVID-19 infection rate, mortality rate, COVID-19 severe infection risk, ventilator use, hospitalization, ICU hospitalization, and recovery time between UDCA group and controls. The secondary outcome was UDCA dose–response association regarding infection risk. We analyzed for odds ratios (ORs), including infection rate, mortality rate, severe infection risk, ventilator use, hospitalization, and intensive care unit hospitalization, and for standardized mean difference (SMD), including recovery time between UDCA groups and controls. Risk of Bias in Non-randomized Studies of Interventions (ROBINS-I) was used to evaluate bias risk.</jats:p>\n </jats:sec>\n <jats:sec>\n <jats:title>Results</jats:title>\n <jats:p>Of 188 articles, 15 cohort studies with 716,310 participants (control = 495,276; UDCA treatment = 221,034) were included. The level of risk of bias was seven studies at low, four at moderate, and four at serious. UDCA showed association with a lower risk of infection (OR, 0.69; 95% CI, 0.55–0.86), lower severe infection risk (OR, 0.75; 95% CI, 0.64–0.89), and ventilator use (OR, 0.75; 95% CI, 0.62–0.90) compared to controls.</jats:p>\n </jats:sec>\n <jats:sec>\n <jats:title>Conclusion</jats:title>\n <jats:p>The findings support evidence for the clinical effects of UDCA for COVID-19 infection. There is a need for randomized trials to evaluate UDCA as a potential prophylactic agent against COVID-19.</jats:p>\n </jats:sec>\n <jats:sec>\n <jats:title>Systematic Review Registration</jats:title>\n <jats:p>\n <jats:ext-link>https://www.crd.york.ac.uk/PROSPERO/view/CRD420251019195</jats:ext-link>\n , identifier #CRD420251019195.\n </jats:p>\n </jats:sec>",
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