SARS-CoV-2 infection in patients with autoimmune hepatitis

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SARS-CoV-2 infection in patients with autoimmune hepatitis. / Marjot, Thomas; Buescher, Gustav; Sebode, Marcial; Barnes, Eleanor; Barritt, Alfred S; Armstrong, Matthew J; Baldelli, Luke; Kennedy, James; Mercer, Carolyn; Ozga, Ann-Kathrin; Casar, Christian; Schramm, Christoph; Moon, Andrew M; Webb, Gwilym J; Lohse, Ansgar W; contributing Members and Collaborators of ERN RARE-LIVER / COVID-Hep / SECURE-Cirrhosis.

In: J HEPATOL, Vol. 74, No. 6, 06.2021, p. 1335-1343.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Marjot, T, Buescher, G, Sebode, M, Barnes, E, Barritt, AS, Armstrong, MJ, Baldelli, L, Kennedy, J, Mercer, C, Ozga, A-K, Casar, C, Schramm, C, Moon, AM, Webb, GJ, Lohse, AW & contributing Members and Collaborators of ERN RARE-LIVER / COVID-Hep / SECURE-Cirrhosis 2021, 'SARS-CoV-2 infection in patients with autoimmune hepatitis', J HEPATOL, vol. 74, no. 6, pp. 1335-1343. https://doi.org/10.1016/j.jhep.2021.01.021

APA

Marjot, T., Buescher, G., Sebode, M., Barnes, E., Barritt, A. S., Armstrong, M. J., Baldelli, L., Kennedy, J., Mercer, C., Ozga, A-K., Casar, C., Schramm, C., Moon, A. M., Webb, G. J., Lohse, A. W., & contributing Members and Collaborators of ERN RARE-LIVER / COVID-Hep / SECURE-Cirrhosis (2021). SARS-CoV-2 infection in patients with autoimmune hepatitis. J HEPATOL, 74(6), 1335-1343. https://doi.org/10.1016/j.jhep.2021.01.021

Vancouver

Marjot T, Buescher G, Sebode M, Barnes E, Barritt AS, Armstrong MJ et al. SARS-CoV-2 infection in patients with autoimmune hepatitis. J HEPATOL. 2021 Jun;74(6):1335-1343. https://doi.org/10.1016/j.jhep.2021.01.021

Bibtex

@article{2488441677d3431f9be4583a612c888f,
title = "SARS-CoV-2 infection in patients with autoimmune hepatitis",
abstract = "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 25th March and 24th October 2020, data were collected for 932 patients with CLD and SARS-CoV-2 infection including 70 with autoimmune hepatitis (AIH). Fifty-eight (83%) patients with AIH were taking ≥1 immunosuppressive drug. There were no differences in rates of major outcomes between patients with AIH and non-AIH CLD, including hospitalization (76% vs. 85%; p = 0.06), intensive care unit admission (29% vs. 23%; p = 0.240), and death (23% vs. 20%; p = 0.643). Factors associated with death within the AIH cohort included age (odds ratio [OR] 2.16/10 years; 1.07-3.81), and Child-Pugh class B (OR 42.48; 4.40-409.53), and C (OR 69.30; 2.83-1694.50) cirrhosis, but not use of immunosuppression. Propensity score matched (PSM) analysis comparing patients with AIH with non-AIH CLD demonstrated no increased risk of adverse outcomes including death (+3.2%; -9.2%-15.7%). PSM analysis of patients with AIH vs. non-CLD (n = 769) demonstrated increased risk of hospitalization with AIH (+18.4%; 5.6-31.2%), but equivalent risk of all other outcomes including death (+3.2%; -9.1%-15.6%).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.",
author = "Thomas Marjot and Gustav Buescher and Marcial Sebode and Eleanor Barnes and Barritt, {Alfred S} and Armstrong, {Matthew J} and Luke Baldelli and James Kennedy and Carolyn Mercer and Ann-Kathrin Ozga and Christian Casar and Christoph Schramm and Moon, {Andrew M} and Webb, {Gwilym J} and Lohse, {Ansgar W} and {contributing Members and Collaborators of ERN RARE-LIVER / COVID-Hep / SECURE-Cirrhosis}",
note = "Copyright {\textcopyright} 2021. Published by Elsevier B.V.",
year = "2021",
month = jun,
doi = "10.1016/j.jhep.2021.01.021",
language = "English",
volume = "74",
pages = "1335--1343",
journal = "J HEPATOL",
issn = "0168-8278",
publisher = "Elsevier",
number = "6",

}

RIS

TY - JOUR

T1 - SARS-CoV-2 infection in patients with autoimmune hepatitis

AU - Marjot, Thomas

AU - Buescher, Gustav

AU - Sebode, Marcial

AU - Barnes, Eleanor

AU - Barritt, Alfred S

AU - Armstrong, Matthew J

AU - Baldelli, Luke

AU - Kennedy, James

AU - Mercer, Carolyn

AU - Ozga, Ann-Kathrin

AU - Casar, Christian

AU - Schramm, Christoph

AU - Moon, Andrew M

AU - Webb, Gwilym J

AU - Lohse, Ansgar W

AU - contributing Members and Collaborators of ERN RARE-LIVER / COVID-Hep / SECURE-Cirrhosis

N1 - Copyright © 2021. Published by Elsevier B.V.

PY - 2021/6

Y1 - 2021/6

N2 - 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 25th March and 24th October 2020, data were collected for 932 patients with CLD and SARS-CoV-2 infection including 70 with autoimmune hepatitis (AIH). Fifty-eight (83%) patients with AIH were taking ≥1 immunosuppressive drug. There were no differences in rates of major outcomes between patients with AIH and non-AIH CLD, including hospitalization (76% vs. 85%; p = 0.06), intensive care unit admission (29% vs. 23%; p = 0.240), and death (23% vs. 20%; p = 0.643). Factors associated with death within the AIH cohort included age (odds ratio [OR] 2.16/10 years; 1.07-3.81), and Child-Pugh class B (OR 42.48; 4.40-409.53), and C (OR 69.30; 2.83-1694.50) cirrhosis, but not use of immunosuppression. Propensity score matched (PSM) analysis comparing patients with AIH with non-AIH CLD demonstrated no increased risk of adverse outcomes including death (+3.2%; -9.2%-15.7%). PSM analysis of patients with AIH vs. non-CLD (n = 769) demonstrated increased risk of hospitalization with AIH (+18.4%; 5.6-31.2%), but equivalent risk of all other outcomes including death (+3.2%; -9.1%-15.6%).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.

AB - 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 25th March and 24th October 2020, data were collected for 932 patients with CLD and SARS-CoV-2 infection including 70 with autoimmune hepatitis (AIH). Fifty-eight (83%) patients with AIH were taking ≥1 immunosuppressive drug. There were no differences in rates of major outcomes between patients with AIH and non-AIH CLD, including hospitalization (76% vs. 85%; p = 0.06), intensive care unit admission (29% vs. 23%; p = 0.240), and death (23% vs. 20%; p = 0.643). Factors associated with death within the AIH cohort included age (odds ratio [OR] 2.16/10 years; 1.07-3.81), and Child-Pugh class B (OR 42.48; 4.40-409.53), and C (OR 69.30; 2.83-1694.50) cirrhosis, but not use of immunosuppression. Propensity score matched (PSM) analysis comparing patients with AIH with non-AIH CLD demonstrated no increased risk of adverse outcomes including death (+3.2%; -9.2%-15.7%). PSM analysis of patients with AIH vs. non-CLD (n = 769) demonstrated increased risk of hospitalization with AIH (+18.4%; 5.6-31.2%), but equivalent risk of all other outcomes including death (+3.2%; -9.1%-15.6%).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.

U2 - 10.1016/j.jhep.2021.01.021

DO - 10.1016/j.jhep.2021.01.021

M3 - SCORING: Journal article

C2 - 33508378

VL - 74

SP - 1335

EP - 1343

JO - J HEPATOL

JF - J HEPATOL

SN - 0168-8278

IS - 6

ER -