Long-term safety of azathioprine for treatment of neuromyelitis optica spectrum disorders

ABSTRACT Background: Azathioprine is a common first-line therapy for neuromyelitis optica spectrum disorder (NMOSD). Objective: The aim of this study was to determine whether long-term treatment (>10 years) with azathioprine is safe in NMOSD. Methods: We conducted a retrospective medical reco...

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Main Authors: Ana Beatriz Ayroza Galvão Ribeiro GOMES, Milena Sales PITOMBEIRA, Douglas Kazutoshi SATO, Dagoberto CALLEGARO, Samira Luisa APÓSTOLOS-PEREIRA
Format: Article
Language:English
Published: Thieme Revinter Publicações 2021-03-01
Series:Arquivos de Neuro-Psiquiatria
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Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2021000300229&tlng=en
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author Ana Beatriz Ayroza Galvão Ribeiro GOMES
Milena Sales PITOMBEIRA
Douglas Kazutoshi SATO
Dagoberto CALLEGARO
Samira Luisa APÓSTOLOS-PEREIRA
author_facet Ana Beatriz Ayroza Galvão Ribeiro GOMES
Milena Sales PITOMBEIRA
Douglas Kazutoshi SATO
Dagoberto CALLEGARO
Samira Luisa APÓSTOLOS-PEREIRA
author_sort Ana Beatriz Ayroza Galvão Ribeiro GOMES
collection DOAJ
description ABSTRACT Background: Azathioprine is a common first-line therapy for neuromyelitis optica spectrum disorder (NMOSD). Objective: The aim of this study was to determine whether long-term treatment (>10 years) with azathioprine is safe in NMOSD. Methods: We conducted a retrospective medical record review of all patients at the School of Medicine of the University of São Paulo (São Paulo, Brazil) who fulfilled the 2015 international consensus diagnostic criteria for NMOSD and were treated with azathioprine for at least 10 years. Results: Out of 375 patients assessed for eligibility, 19 were included in this analysis. These patients’ median age was 44 years (range=28-61); they were mostly female (17/19) and AQP4-IgG seropositive (18/19). The median disease duration was 15 years (range=10-39) and most patients presented a relapsing clinical course (84.2%). The median duration of treatment was 11.9 years (range=10.0-23.8). The median annualized relapse rates (ARR) pre- and post-treatment with azathioprine were 1 (range=0.1-2) and 0.1 (range=0-0.35); p=0.09. Three patients (15.7%) had records of adverse events during the follow-up, which consisted of chronic B12 vitamin deficiency, pulmonary tuberculosis and breast cancer. Conclusion: Azathioprine may be considered a safe agent for long-term treatment (>10 years) of NMOSD, but continuous vigilance for infections and malignancies is required.
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spelling doaj-art-b0ec3ccace3e4dcbbd0081aab69f1dcd2025-08-20T03:39:25ZengThieme Revinter PublicaçõesArquivos de Neuro-Psiquiatria1678-42272021-03-0179322923210.1590/0004-282x-anp-2020-0041Long-term safety of azathioprine for treatment of neuromyelitis optica spectrum disordersAna Beatriz Ayroza Galvão Ribeiro GOMEShttps://orcid.org/0000-0003-1657-6891Milena Sales PITOMBEIRAhttps://orcid.org/0000-0002-3298-0264Douglas Kazutoshi SATOhttps://orcid.org/0000-0002-7695-6020Dagoberto CALLEGAROhttps://orcid.org/0000-0003-0077-173XSamira Luisa APÓSTOLOS-PEREIRAhttps://orcid.org/0000-0003-3493-1199ABSTRACT Background: Azathioprine is a common first-line therapy for neuromyelitis optica spectrum disorder (NMOSD). Objective: The aim of this study was to determine whether long-term treatment (>10 years) with azathioprine is safe in NMOSD. Methods: We conducted a retrospective medical record review of all patients at the School of Medicine of the University of São Paulo (São Paulo, Brazil) who fulfilled the 2015 international consensus diagnostic criteria for NMOSD and were treated with azathioprine for at least 10 years. Results: Out of 375 patients assessed for eligibility, 19 were included in this analysis. These patients’ median age was 44 years (range=28-61); they were mostly female (17/19) and AQP4-IgG seropositive (18/19). The median disease duration was 15 years (range=10-39) and most patients presented a relapsing clinical course (84.2%). The median duration of treatment was 11.9 years (range=10.0-23.8). The median annualized relapse rates (ARR) pre- and post-treatment with azathioprine were 1 (range=0.1-2) and 0.1 (range=0-0.35); p=0.09. Three patients (15.7%) had records of adverse events during the follow-up, which consisted of chronic B12 vitamin deficiency, pulmonary tuberculosis and breast cancer. Conclusion: Azathioprine may be considered a safe agent for long-term treatment (>10 years) of NMOSD, but continuous vigilance for infections and malignancies is required.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2021000300229&tlng=enAzathioprineNeuromyelitis OpticaTherapeutics
spellingShingle Ana Beatriz Ayroza Galvão Ribeiro GOMES
Milena Sales PITOMBEIRA
Douglas Kazutoshi SATO
Dagoberto CALLEGARO
Samira Luisa APÓSTOLOS-PEREIRA
Long-term safety of azathioprine for treatment of neuromyelitis optica spectrum disorders
Arquivos de Neuro-Psiquiatria
Azathioprine
Neuromyelitis Optica
Therapeutics
title Long-term safety of azathioprine for treatment of neuromyelitis optica spectrum disorders
title_full Long-term safety of azathioprine for treatment of neuromyelitis optica spectrum disorders
title_fullStr Long-term safety of azathioprine for treatment of neuromyelitis optica spectrum disorders
title_full_unstemmed Long-term safety of azathioprine for treatment of neuromyelitis optica spectrum disorders
title_short Long-term safety of azathioprine for treatment of neuromyelitis optica spectrum disorders
title_sort long term safety of azathioprine for treatment of neuromyelitis optica spectrum disorders
topic Azathioprine
Neuromyelitis Optica
Therapeutics
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2021000300229&tlng=en
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