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Autoimmune hepatitis in patients with multiple sclerosis: The role of immunomodulatory treatment

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Autor
Rigopoulou E.I., Gyftaki S., Arvaniti P., Tsimourtou V., Koukoulis G.K., Hadjigeorgiou G., Dalekos G.N.
Fecha
2019
Language
en
DOI
10.1016/j.clinre.2018.12.002
Materia
alanine aminotransferase
aspartate aminotransferase
azathioprine
beta interferon
immunoglobulin G
methylprednisolone
mycophenolate mofetil
prednisolone
autoantibody
azathioprine
beta interferon
glucocorticoid
immunologic factor
immunosuppressive agent
methylprednisolone
mycophenolic acid
prednisolone
adult
alanine aminotransferase blood level
Article
aspartate aminotransferase blood level
autoimmune hepatitis
clinical article
controlled study
demography
differential diagnosis
disease activity
disease association
disease exacerbation
drug dose reduction
drug megadose
female
follow up
human
immunomodulation
liver function test
male
multiple sclerosis
prospective study
remission
scoring system
treatment duration
treatment response
autoimmune hepatitis
blood
complication
multiple sclerosis
Adult
Autoantibodies
Azathioprine
Female
Glucocorticoids
Hepatitis, Autoimmune
Humans
Immunologic Factors
Immunosuppressive Agents
Interferon-beta
Liver Function Tests
Male
Methylprednisolone
Multiple Sclerosis
Mycophenolic Acid
Prednisolone
Elsevier Masson SAS
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Resumen
Background: Development of autoimmune hepatitis (AIH) has been sporadically reported in patients with multiple sclerosis (MS) either concurrently or after treatment with immunomodulatory drugs, including interferon-beta (IFN-β) and steroids. Aim: To report a large cohort of 14 patients with MS diagnosed with AIH during an assessment of deranged liver function tests (LFTs). Patients and methods: From 2005 to 2017, we prospectively identified 14 (13 women) patients with MS who suffered also from AIH after investigation in our department for the presence of deranged LFTs. Age at diagnosis of MS was 36.7 ± 9.3 years while at diagnosis of AIH 43.1 ± 12 years. Results: AIH diagnosis was based on elevation of aminotransferases in all patients [alanine aminotransferase: 520 IU/L (range: 115–1219)], elevation of IgG in 6, compatible autoantibody profile in all, including 5 patients with liver-specific autoantibodies and typical or compatible histological features in 11 patients. 5 patients were under treatment with IFN-β plus methylprednisolone pulses, 3 with IFN-β plus oral steroids, 1 with IFN-β, 4 with methylprednisolone pulses whereas 1 patient was free of treatment. The median time from IFN-β initiation to the development of hepatitis was 12 months (range:1–120). Treatment for AIH was initiated in 13 patients with prednisolone (0.5–1 mg/kg/day) plus mycophenolate myfetil (2 g/day) in 10 and prednisolone plus azathioprine in 3 with complete and partial response in 11 and 2 patients, respectively. Conclusions: The differential diagnosis of hepatitis in MS patients should include AIH and in particular when immunomodulatory treatment has been preceded. Autoantibody testing and liver histology play fundamental role in establishing a prompt diagnosis of AIH in these patients. Treatment of AIH in patients with MS seems safe and efficient as complete or partial response was recorded in all of our patients. © 2018 Elsevier Masson SAS
URI
http://hdl.handle.net/11615/78509
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]
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