Adverse events related to low dose corticosteroids in autoimmune hepatitis.


Journal

Alimentary pharmacology & therapeutics
ISSN: 1365-2036
Titre abrégé: Aliment Pharmacol Ther
Pays: England
ID NLM: 8707234

Informations de publication

Date de publication:
11 2019
Historique:
received: 26 06 2019
revised: 20 07 2019
accepted: 16 09 2019
pubmed: 17 10 2019
medline: 26 5 2020
entrez: 17 10 2019
Statut: ppublish

Résumé

Autoimmune hepatitis requires long-term therapy, and systemic corticosteroids are the backbone of therapeutic management. Prolonged use of corticosteroids may lead to adverse events but data from long-term studies are mainly derived from studies in rheumatic diseases. To assess cataract, diabetes and fractures in relation to corticosteroid doses in the long-term maintenance treatment of patients with autoimmune hepatitis. We retrospectively collected data on 476 patients (77% women) with an established diagnosis of autoimmune hepatitis. Binary logistic regression with a generalised estimating equation was used to analyse the association between current corticosteroid use and the incidence of cataract, diabetes and fractures with onset after autoimmune hepatitis diagnosis. We corrected for sex, age, cirrhosis at diagnosis and predniso(lo)ne use in the prior 3 years to account for possible ongoing effects. A total of 6634 years, with a median of 13 (range 1-40) per patient were recorded. The median age at diagnosis was 44 years (range 2-88). Adverse events were documented in 120 (25%) patients. Low-dose predniso(lo)ne (0.1-5.0 mg/d) increased the odds of fractures whereas higher doses (>5.0 mg/d) increased the odds of cataracts and diabetes. Budesonide increased the odds of cataract and fractures; this effect was independent of predniso(lo)ne use in the prior 1, 2 or 3 years. Even low doses of corticosteroids frequently lead to substantial adverse events refuting the assumption that adverse events are prevented by administering low doses.

Sections du résumé

BACKGROUND
Autoimmune hepatitis requires long-term therapy, and systemic corticosteroids are the backbone of therapeutic management. Prolonged use of corticosteroids may lead to adverse events but data from long-term studies are mainly derived from studies in rheumatic diseases.
AIM
To assess cataract, diabetes and fractures in relation to corticosteroid doses in the long-term maintenance treatment of patients with autoimmune hepatitis.
METHODS
We retrospectively collected data on 476 patients (77% women) with an established diagnosis of autoimmune hepatitis. Binary logistic regression with a generalised estimating equation was used to analyse the association between current corticosteroid use and the incidence of cataract, diabetes and fractures with onset after autoimmune hepatitis diagnosis. We corrected for sex, age, cirrhosis at diagnosis and predniso(lo)ne use in the prior 3 years to account for possible ongoing effects.
RESULTS
A total of 6634 years, with a median of 13 (range 1-40) per patient were recorded. The median age at diagnosis was 44 years (range 2-88). Adverse events were documented in 120 (25%) patients. Low-dose predniso(lo)ne (0.1-5.0 mg/d) increased the odds of fractures whereas higher doses (>5.0 mg/d) increased the odds of cataracts and diabetes. Budesonide increased the odds of cataract and fractures; this effect was independent of predniso(lo)ne use in the prior 1, 2 or 3 years.
CONCLUSIONS
Even low doses of corticosteroids frequently lead to substantial adverse events refuting the assumption that adverse events are prevented by administering low doses.

Identifiants

pubmed: 31617229
doi: 10.1111/apt.15528
pmc: PMC6899908
doi:

Substances chimiques

Adrenal Cortex Hormones 0
Glucocorticoids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1120-1126

Investigateurs

N M van Gerven (NM)
J Ph Kuijvenhoven (JP)
T C M A Schreuder (TCMA)
E J van der Wouden (EJ)
J J M van Meyel (JJM)
L C Baak (LC)
P H G M Stadhouders (PHGM)
M Klemt-Kropp (M)
M A M T Verhagen (MAMT)
A Bhalla (A)
J W den Ouden (JW)
U Beuers (U)
K J van Erpecum (KJ)
H R van Buuren (HR)
J T Brouwer (JT)

Informations de copyright

© 2019 The Authors. Alimentary Pharmacology & Therapeutics published by John Wiley & Sons Ltd.

Références

Clin Gastroenterol Hepatol. 2016 Mar;14(3):445-53
pubmed: 26492846
Aliment Pharmacol Ther. 2019 Mar;49(5):528-536
pubmed: 30671977
Clin Ther. 2011 Oct;33(10):1413-32
pubmed: 21999885
Aliment Pharmacol Ther. 2019 Nov;50(10):1120-1126
pubmed: 31617229
Aliment Pharmacol Ther. 2018 Oct;48(7):761-767
pubmed: 30109891
Respir Res. 2018 Apr 27;19(1):75
pubmed: 29699563
Clin Gastroenterol Hepatol. 2019 Apr;17(5):940-947.e2
pubmed: 30291909
Aliment Pharmacol Ther. 2017 Mar;45(5):723-732
pubmed: 28004405
Gut. 1973 May;14(5):419
pubmed: 4123775
J Hepatol. 2013 Jan;58(1):141-7
pubmed: 22989569
J Bone Miner Res. 2000 Jun;15(6):993-1000
pubmed: 10841167
Aliment Pharmacol Ther. 2013 Mar;37(6):640-6
pubmed: 23347359
J Hepatol. 2011 Feb;54(2):374-85
pubmed: 21067838
Clin Pharmacokinet. 2004;43(12):803-21
pubmed: 15355126
World J Gastroenterol. 2016 May 21;22(19):4651-61
pubmed: 27217697
J Hepatol. 2011 Sep;55(3):636-646
pubmed: 21238519
Q J Med. 1971 Apr;40(158):159-85
pubmed: 4933363
Allergy Asthma Proc. 2016 Nov;37(6):458-465
pubmed: 27931301
J Hepatol. 2011 Jul;55(1):171-82
pubmed: 21167232
Gut. 1975 Nov;16(11):876-83
pubmed: 1104411
Ann Rheum Dis. 2009 Jul;68(7):1119-24
pubmed: 18684744
Gastroenterology. 2010 Oct;139(4):1198-206
pubmed: 20600032
Gastroenterology. 1972 Nov;63(5):820-33
pubmed: 4538724
J Hepatol. 2015 Oct;63(4):971-1004
pubmed: 26341719
Arthritis Rheum. 2004 Nov;50(11):3408-17
pubmed: 15529366
Am J Med. 1994 Feb;96(2):115-23
pubmed: 8109596
Dig Dis. 2013;31(3-4):368-73
pubmed: 24246990
J Hepatol. 2010 Jul;53(1):191-8
pubmed: 20400196
Aliment Pharmacol Ther. 1994 Dec;8(6):585-90
pubmed: 7696446
Clin Ther. 2013 Apr;35(4):486-97
pubmed: 23587268
Scand J Gastroenterol. 2014 Oct;49(10):1245-54
pubmed: 25123213
Dig Dis. 2015;33 Suppl 2:88-93
pubmed: 26641661
J Hepatol. 1999 Nov;31(5):929-38
pubmed: 10580593

Auteurs

Floris F van den Brand (FF)

Department of Gastroenterology and Hepatology, Amsterdam UMC, Location VUmc, Amsterdam, The Netherlands.

Koen S van der Veen (KS)

Department of Gastroenterology and Hepatology, Amsterdam UMC, Location VUmc, Amsterdam, The Netherlands.

Birgit I Lissenberg-Witte (BI)

Department of Epidemiology and Biostatistics, Amsterdam UMC, Location VUmc, Amsterdam, The Netherlands.

Ynto S de Boer (YS)

Department of Gastroenterology and Hepatology, Amsterdam UMC, Location VUmc, Amsterdam, The Netherlands.

Bart van Hoek (B)

Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.

Joost P H Drenth (JPH)

Department of Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen, The Netherlands.

Robert C Verdonk (RC)

Department of Gastroenterology and Hepatology, Sint Antonius Hospital, Nieuwegein, The Netherlands.

Jan M Vrolijk (JM)

Department of Gastroenterology and Hepatology, Rijnstate Hospital, Arnhem, The Netherlands.

Carin M J van Nieuwkerk (CMJ)

Department of Gastroenterology and Hepatology, Amsterdam UMC, Location VUmc, Amsterdam, The Netherlands.

Gerd Bouma (G)

Department of Gastroenterology and Hepatology, Amsterdam UMC, Location VUmc, Amsterdam, The Netherlands.

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