4.7 Article

Ursodeoxycholic acid administration did not reduce susceptibility to SARS-CoV-2 infection in children

Journal

LIVER INTERNATIONAL
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1111/liv.15660

Keywords

COVID-19; SARS-CoV-2; UDCA

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A recent study investigated the effects of ursodeoxycholic acid (UDCA) administration on susceptibility to SARS-CoV-2 infection in children with liver disease. A questionnaire was distributed to 300 families, and the proportion of families with SARS-CoV-2 infection was compared between children taking and not taking UDCA. The results suggest that UDCA administration does not reduce susceptibility to SARS-CoV-2 infection in children with liver disease.
Background and AimsA recent study suggested that administration of ursodeoxycholic acid (UDCA) at dosages usually employed clinically may reduce rates of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. A recent surge of SARS-CoV-2 omicron infection in China allowed study of whether UDCA administration reduced susceptibility to SARS-CoV-2 infection in children with liver disease. MethodsThrough WeChat groups, a questionnaire was distributed to families (n = 300) in which a child had been admitted to our liver service in the past 5 years. The proportion of families in which both a liver service child and another family or household member were infected with SARS-CoV-2 was compared between families in which children were and were not taking UDCA. ResultsOf the 300 questionnaire answers, 280 (93.3%) were valid. SARS-CoV-2 infection was confirmed in 226 families (80.7%): 146 children were taking UDCA (10-20 mg/kg/day) and 80 children were not taking UDCA. SARS-CoV-2 infection was confirmed in 95 children taking UDCA (65.1%) and in 51 children not taking UDCA (63.8%) (p = 0.843); SARS-CoV-2 infection was suspected in 23 children taking UDCA (15.8%) and in 11 children not taking UDCA (13.8%) (p = 0.687). ConclusionsThese results indicate that UDCA administration does not reduce susceptibility to SARS-CoV-2 infection in children with liver disease.

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