Effects of Immunosuppressive Drugs on Covid-19 Severity in Patients With Autoimmune Hepatitis

Abstract

Background We investigated associations between baseline use of immunosuppressive drugs and severity of Coronavirus Disease 2019 (COVID-19) in autoimmune hepatitis (AIH). Patients and methods Data of AIH patients with laboratory confirmed COVID-19 were retrospectively collected from 15 countries. The outcomes of AIH patients who were on immunosuppression at the time of COVID-19 were compared to patients who were not on AIH medication. The clinical courses of COVID-19 were classified as (i)-no hospitalization, (ii)-hospitalization without oxygen supplementation, (iii)-hospitalization with oxygen supplementation by nasal cannula or mask, (iv)-intensive care unit (ICU) admission with non-invasive mechanical ventilation, (v)-ICU admission with invasive mechanical ventilation or (vi)-death and analysed using ordinal logistic regression. Results We included 254 AIH patients (79.5%, female) with a median age of 50 (range, 17-85) years. At the onset of COVID-19, 234 patients (92.1%) were on treatment with glucocorticoids (n = 156), thiopurines (n = 151), mycophenolate mofetil (n = 22) or tacrolimus (n = 16), alone or in combinations. Overall, 94 (37%) patients were hospitalized and 18 (7.1%) patients died. Use of systemic glucocorticoids (adjusted odds ratio [aOR] 4.73, 95% CI 1.12-25.89) and thiopurines (aOR 4.78, 95% CI 1.33-23.50) for AIH was associated with worse COVID-19 severity, after adjusting for age-sex, comorbidities and presence of cirrhosis. Baseline treatment with mycophenolate mofetil (aOR 3.56, 95% CI 0.76-20.56) and tacrolimus (aOR 4.09, 95% CI 0.69-27.00) were also associated with more severe COVID-19 courses in a smaller subset of treated patients. Conclusion Baseline treatment with systemic glucocorticoids or thiopurines prior to the onset of COVID-19 was significantly associated with COVID-19 severity in patients with AIH.

Description

Eren, Fatih/0000-0003-2667-8963; Magro, Bianca/0000-0002-6417-3205; Cristoferi, Laura/0000-0001-9846-7474; Rigamonti, Cristina/0000-0003-2089-4139; Dhanasekaran, Renumathy/0000-0001-8819-7511; Peralta, Mirta/0000-0003-4946-0190; Demir, Nurhan/0000-0003-0037-7775; Lytvyak, Ellina/0000-0001-5651-9010; Barutcu, Sezgin/0000-0003-0823-3215; Kacmaz, Huseyin/0000-0001-6788-3459; Efe, Cumali/0000-0001-6593-5702; Eskazan, Tugce/0000-0003-3008-1940; Ebik, Berat/0000-0002-0012-2505; Satapathy, Sanjaya/0000-0003-0153-2829; Urzua, Alvaro/0000-0002-8059-8844; Gerussi, Alessio/0000-0002-5086-0514; Guzelbulut, Fatih/0000-0003-4889-208X; Gomez-Aldana, Andres Jose/0000-0002-7954-4910; Wahlin, Staffan/0000-0002-5985-9464; Drenth, Joost Ph/0000-0001-8027-3073; Higuera-De La Tjera, Fatima/0000-0003-3870-0478; Alvares-Da-Silva, Mario/0000-0002-5001-246X

Keywords

Autoimmunity, Azathioprine, Budesonide, Liver Transplantation, Mercaptopurine, Sars-Cov-2

Turkish CoHE Thesis Center URL

WoS Q

Q1

Scopus Q

Q1

Source

Volume

42

Issue

3

Start Page

607

End Page

614
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