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In Vitro Modeling of Fat Deposition in Metabolic Dysfunction-Associated Steatotic Liver Disease
Published on: July 19, 2024
Ursodeoxycholic acid and long COVID in steatotic liver disease: a nationwide cohort study
Kyungyeon Jung1, Gi-Ae Kim2, Jieun Woo1
1Department of Biohealth Regulatory Science, Sungkyunkwan University, Suwon, Korea.
Insights
Ursodeoxycholic acid (UDCA) did not prevent most long COVID outcomes in patients with steatotic liver disease (SLD). While it showed a protective effect for atrial fibrillation, UDCA use was linked to increased risks of type 2 diabetes and epilepsy.
Area of Science:
- Hepatology
- Infectious Diseases
- Cardiology
- Endocrinology
- Neurology
Background:
- Ursodeoxycholic acid (UDCA) may reduce acute COVID-19 severity by downregulating the SARS-CoV-2 entry receptor ACE2.
- Steatotic liver disease (SLD) patients are vulnerable to adverse COVID-19 outcomes, but UDCA's effect on long COVID in this group is unknown.
Purpose of the Study:
- To investigate the association between pre-infection UDCA use and the risk of developing long COVID conditions in patients with SLD.
Main Methods:
- Nationwide retrospective cohort study using Korean COVID-19 registry and National Health Insurance Service data (2019-2022).
- Included patients with SLD (fatty liver index ≥30) who had COVID-19.
- Assessed UDCA use within 90 days pre-infection and 20 long COVID outcomes ≥84 days post-infection.
- Used propensity score fine stratification and Cox regression to estimate hazard ratios.
Main Results:
- Among 469,108 SLD patients with COVID-19, 5.0% used UDCA.
- UDCA use was not associated with reduced risk for most long COVID outcomes.
- A protective association was found for atrial fibrillation (HR 0.51).
- Increased risks were observed for type 2 diabetes mellitus (HR 1.24) and epilepsy (HR 1.69).
Conclusions:
- Pre-infection UDCA use does not appear to reduce the risk of most long COVID outcomes in patients with SLD.
- Observed associations require cautious interpretation due to potential residual confounding and surveillance bias.
Background/Aims:
Ursodeoxycholic acid (UDCA) downregulates angiotensin-converting enzyme 2, the cellular entry receptor for SARS-CoV-2, and may reduce acute coronavirus disease 2019 (COVID-19) severity. However, it remains unknown whether UDCA prevents long COVID outcomes in patients with steatotic liver disease (SLD)-a population vulnerable to adverse outcomes. We investigated the association between pre-infection UDCA use and risk of long COVID outcomes in patients with SLD.
Methods:
We conducted a nationwide retrospective cohort study using the Korean COVID-19 registry linked to National Health Insurance Service claims data (2019-2022). Patients with SLD (fatty liver index ≥30) who experienced COVID-19 were included. Exposure was defined as at least one UDCA prescription within the 90 days preceding infection. Outcomes of interest were 20 incident long COVID conditions across eight organ systems assessed ≥84 days post-infection. After propensity score (PS) fine stratification, hazard ratios (HR) with 95% confidence intervals (CI) were estimated using Cox regression.
Results:
Among 469,108 patients with SLD and COVID-19, 23,560 (5.0%) were UDCA users. After PS fine stratification weighting, UDCA use was not associated with reduced risk for most long COVID outcomes. A protective association was observed for atrial fibrillation (HR 0.51, 95% CI 0.30-0.88), whereas increased risks were found for type 2 diabetes mellitus (HR 1.24, 95% CI 1.09-1.42) and epilepsy (HR 1.69, 95% CI 1.09-2.61).
Conclusions:
Pre-infection UDCA use was not associated with reduced risk for most long COVID outcomes in patients with SLD. The observed associations warrant cautious interpretation given potential residual confounding and surveillance bias.
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