Oral Ursodeoxycholic Acid Therapy Failed to Mitigate SARS-CoV-2 Omicron Infection

Author:

Yu Dong-Shan1,Song Zhi-Ying1,Liu Yun1,Zhu Guo-Jian1,Sun Ke1,Li Yan-Hua2,Yu Rong-Yan1,Xi Wen-Na1

Affiliation:

1. The Second Affiliated Hospital of Nanchang University

2. Chinese Academy of Sciences (CAS)

Abstract

Abstract

Background Ursodeoxycholic acid (UDCA) was reported to reduce susceptibility to SARS-CoV-2 infection by downregulating farnesoid X receptor (FXR) -ACE2 signaling. However, we found a different story in real-world clinical studies. Methods We attempted to verify whether UDCA can effectively prevent SARS-CoV-2 transmission or have positive therapeutic effects in a real-world clinical study. We performed a retrospective study, collected, and assessed clinical presentation and laboratory data on patients with liver diseases infected with SARS-CoV-2 Omicron sub-variant BA.5.2 who had been treated with or without UDCA, patients treated with UDCA without SARS-CoV-2 infection were set as control group. Results The data showed treatment with UDCA did not prevent infection with the Omicron sub-variant BA.5.2, failed in reducing the duration of infection and hardly mitigated the severity of COVID-19. Meanwhile, the severity of liver diseases, especially TBil, ALP, γ-GT, liver cirrhosis and Child-Pugh classification, should be considered as risk factors for severe COVID-19 in chronic hepatic patients. Conclusion UDCA failed to show inhibitory effects against SARS-CoV-2 infection in complex clinical settings. The regulatory mechanism of the novel UDCA-FXR-ACE2 pathway needs to be further investigated in real-world clinical studies.

Publisher

Springer Science and Business Media LLC

Reference10 articles.

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2. SARS-CoV-2, ACE2 expression, and systemic organ invasion;Ashraf UM,2021

3. FXR inhibition may protect from SARS-CoV-2 infection by reducing ACE2;Brevini T,2022

4. SARS-CoV-2 infection in patients with a normal or abnormal liver;Cabibbo G,2021

5. COVID-19 and liver disease;Dufour JF,2022

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