SARS-CoV-2 infection in patients with autoimmune hepatitis.


Journal

Journal of hepatology
ISSN: 1600-0641
Titre abrégé: J Hepatol
Pays: Netherlands
ID NLM: 8503886

Informations de publication

Date de publication:
06 2021
Historique:
received: 01 12 2020
revised: 24 12 2020
accepted: 12 01 2021
pubmed: 29 1 2021
medline: 26 5 2021
entrez: 28 1 2021
Statut: ppublish

Résumé

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and coronavirus disease 2019 (COVID-19) continues to have a devastating impact across the globe. However, little is known about the disease course in patients with autoimmune hepatitis (AIH). Data for patients with AIH and SARS-CoV-2 infection were combined from 3 international reporting registries and outcomes were compared to those in patients with chronic liver disease of other aetiology (non-AIH CLD) and to patients without liver disease (non-CLD). Between 25 Patients with AIH were not at increased risk of adverse outcomes despite immunosuppressive treatment compared to other causes of CLD and to matched cases without liver disease. Little is known about the outcomes of COVID-19 in patients with autoimmune hepatitis (AIH), a rare chronic inflammatory liver disease. This study combines data from 3 large registries to describe the course of COVID-19 in this patient group. We show that AIH patients do not appear to have an increased risk of death from COVID-19 compared to patients with other forms of liver disease and compared to patients without liver disease, despite the use of medications which suppress the immune system.

Sections du résumé

BACKGROUND & AIMS
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and coronavirus disease 2019 (COVID-19) continues to have a devastating impact across the globe. However, little is known about the disease course in patients with autoimmune hepatitis (AIH).
METHODS
Data for patients with AIH and SARS-CoV-2 infection were combined from 3 international reporting registries and outcomes were compared to those in patients with chronic liver disease of other aetiology (non-AIH CLD) and to patients without liver disease (non-CLD).
RESULTS
Between 25
CONCLUSION
Patients with AIH were not at increased risk of adverse outcomes despite immunosuppressive treatment compared to other causes of CLD and to matched cases without liver disease.
LAY SUMMARY
Little is known about the outcomes of COVID-19 in patients with autoimmune hepatitis (AIH), a rare chronic inflammatory liver disease. This study combines data from 3 large registries to describe the course of COVID-19 in this patient group. We show that AIH patients do not appear to have an increased risk of death from COVID-19 compared to patients with other forms of liver disease and compared to patients without liver disease, despite the use of medications which suppress the immune system.

Identifiants

pubmed: 33508378
pii: S0168-8278(21)00033-7
doi: 10.1016/j.jhep.2021.01.021
pmc: PMC7835076
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1335-1343

Subventions

Organisme : NIDDK NIH HHS
ID : T32 DK007634
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002489
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002489
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2021 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest The authors do not have any conflicts of interest. Please refer to the accompanying ICMJE disclosure forms for further details.

Références

N Engl J Med. 2021 Feb 25;384(8):693-704
pubmed: 32678530
Gut. 2021 Apr;70(4):725-732
pubmed: 33082265
BMJ. 2017 May 23;357:j2099
pubmed: 28536104
Hepatology. 2020 Jul;72(1):287-304
pubmed: 32298473
Clin Gastroenterol Hepatol. 2020 Sep;18(10):2369-2371.e1
pubmed: 32480009
Am J Transplant. 2020 Nov;20(11):3008-3018
pubmed: 32780493
Lancet Gastroenterol Hepatol. 2020 Nov;5(11):1008-1016
pubmed: 32866433
Nature. 2020 Aug;584(7821):430-436
pubmed: 32640463
Hepatol Commun. 2020 Jun 09;:
pubmed: 32838102
Clin Gastroenterol Hepatol. 2020 Sep 17;:
pubmed: 32950749
J Hepatol. 2020 Sep;73(3):702-705
pubmed: 32413378
Ann Rheum Dis. 2020 Jul;79(7):859-866
pubmed: 32471903
Int J Infect Dis. 2020 May;94:91-95
pubmed: 32173574
JHEP Rep. 2020 Oct;2(5):100169
pubmed: 32835190
Scand J Gastroenterol. 2008;43(10):1232-40
pubmed: 18609163
J Hepatol. 2021 Jan;74(1):148-155
pubmed: 32750442
J Hepatol. 2020 Nov;73(5):1063-1071
pubmed: 32526252
J Hepatol. 2021 Mar;74(3):567-577
pubmed: 33035628
Health Serv Res. 2014 Oct;49(5):1701-20
pubmed: 24779867
J Hepatol. 2014 Mar;60(3):612-7
pubmed: 24326217
Gut. 2021 Mar;70(3):531-536
pubmed: 32660964

Auteurs

Thomas Marjot (T)

Oxford Liver Unit, Translational Gastroenterology Unit, Oxford University Hospitals NHS Foundation Trust, University of Oxford, Oxford, UK. Electronic address: thomas.marjot@ndm.ox.ac.uk.

Gustav Buescher (G)

Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany; European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany.

Marcial Sebode (M)

Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany; European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany.

Eleanor Barnes (E)

Oxford Liver Unit, Translational Gastroenterology Unit, Oxford University Hospitals NHS Foundation Trust, University of Oxford, Oxford, UK.

A Sidney Barritt (AS)

Division of Gastroenterology and Hepatology, University of North Carolina, Chapel Hill, North Carolina, USA.

Matthew J Armstrong (MJ)

Liver Unit, Queen Elizabeth Hospital Birmingham, Birmingham, UK.

Luke Baldelli (L)

Department of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA.

James Kennedy (J)

Oxford Liver Unit, Translational Gastroenterology Unit, Oxford University Hospitals NHS Foundation Trust, University of Oxford, Oxford, UK.

Carolyn Mercer (C)

Oxford Liver Unit, Translational Gastroenterology Unit, Oxford University Hospitals NHS Foundation Trust, University of Oxford, Oxford, UK.

Ann-Kathrin Ozga (AK)

Institute of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Christian Casar (C)

Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany; European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany.

Christoph Schramm (C)

Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany; European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany; Martin Zeitz Centre for Rare Diseases, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.

Andrew M Moon (AM)

Division of Gastroenterology and Hepatology, University of North Carolina, Chapel Hill, North Carolina, USA.

Gwilym J Webb (GJ)

Cambridge Liver Unit, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK.

Ansgar W Lohse (AW)

Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany; European Reference Network on Hepatological Diseases (ERN RARE-LIVER), Germany. Electronic address: alohse@uke.de.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH