Late Onset of Neuromyelitis Optica Spectrum Disorders

Abstract Introduction Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune demyelinating disease of the central nervous system. NMOSD starting after the age of 50 years is considered a “late onset” (LO-NMOSD) and seems to be particularly aggressive. The objective of this paper is to prese...

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Main Authors: Yara Dadalti Fragoso, Heloisa Helena Ruocco, Ronaldo Maciel Dias, Hideraldo Cabeça, Ricardo Gonçalves, Nise A. de Carvalho Sousa, Caroline Vieira Spessotto, Carlos Bernardo Tauil, Soniza Vieira Alves-Leon, Sidney Gomes, Marcus Vinicius M. Gonçalves, Suzana C. Nunes Machado, Andrea Anacleto, Eber Castro Correa, Maria Lucia V. Pimentel, Gutemberg Augusto C. Santos
Format: Article
Language:English
Published: Adis, Springer Healthcare 2019-07-01
Series:Neurology and Therapy
Subjects:
Online Access:http://link.springer.com/article/10.1007/s40120-019-0143-2
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spelling doaj-10a7da463195421a85652b034d211d4c2020-11-25T03:37:33ZengAdis, Springer HealthcareNeurology and Therapy2193-82532193-65362019-07-018247748210.1007/s40120-019-0143-2Late Onset of Neuromyelitis Optica Spectrum DisordersYara Dadalti Fragoso0Heloisa Helena Ruocco1Ronaldo Maciel Dias2Hideraldo Cabeça3Ricardo Gonçalves4Nise A. de Carvalho Sousa5Caroline Vieira Spessotto6Carlos Bernardo Tauil7Soniza Vieira Alves-Leon8Sidney Gomes9Marcus Vinicius M. Gonçalves10Suzana C. Nunes Machado11Andrea Anacleto12Eber Castro Correa13Maria Lucia V. Pimentel14Gutemberg Augusto C. Santos15Department of Neurology, Universidade Metropolitana de SantosDepartment of Neurology, Pontificia Universidade Catolica de CampinasDepartment of Neurology, Hospital de Base do Distrito FederalDepartment of Neurology, Hospital Ophir LoyolaDepartment of Neurology, Hospital PompeiaDepartment of Neurology, University Hospital Getulio VargasDepartment of Neurology, Santa Casa Misericordia de AracatubaDepartment of Neurology, Hospital de Base do Distrito FederalDepartment of Neurology, Universidade Federal do Rio de JaneiroDepartment of Neurology, Hospital Beneficencia Portuguesa de Sao Paulo and Hospital PaulistanoDepartment of Neurology, Universidade da Regiao de JoinvilleDepartment of Neurology, Hospital de CaridadeDepartment of Neurology, Universidade Metropolitana de SantosDepartment of Neurology, Hospital de Base do Distrito FederalDepartment of Neurology, Santa Casa de Misericordia do Rio de JaneiroDepartment of Neurology, Universidade Estacio de SaAbstract Introduction Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune demyelinating disease of the central nervous system. NMOSD starting after the age of 50 years is considered a “late onset” (LO-NMOSD) and seems to be particularly aggressive. The objective of this paper is to present a series of 37 Brazilian patients with LO-NMOSD. Methods Retrospective data collection from medical records of patients with LO-NMOSD seen at 14 Brazilian specialized units. Results The ratio of women to men in the sample was 4.3 to 1. The patients were followed up for a median period of 4 years. Sex, age at disease onset, and ethnic background were not associated with the number of relapses or disability outcomes. Extensive longitudinal myelitis affected 86% of patients, while optic neuritis affected 70%, and brainstem syndromes were present in only 16% of these patients. Six patients are currently using some type of support for walking or are wheelchair-bound. Three have died. Therapeutic options for NMOSD were particularly complicated for these elderly patients, since medications for controlling NMOSD are, in essence, immunosuppressive. Long-term use of corticosteroids can be an issue when the patients have high blood pressure, diabetes mellitus, or dyslipidemia (conditions often seen in elderly individuals). Conclusion This series of LO-NMOSD cases highlights the importance of prompt diagnosis and treatment for these patients.http://link.springer.com/article/10.1007/s40120-019-0143-2ElderlyDisabilityNeurologyNeuromyelitis opticaNeuromyelitis optica spectrum disorders
collection DOAJ
language English
format Article
sources DOAJ
author Yara Dadalti Fragoso
Heloisa Helena Ruocco
Ronaldo Maciel Dias
Hideraldo Cabeça
Ricardo Gonçalves
Nise A. de Carvalho Sousa
Caroline Vieira Spessotto
Carlos Bernardo Tauil
Soniza Vieira Alves-Leon
Sidney Gomes
Marcus Vinicius M. Gonçalves
Suzana C. Nunes Machado
Andrea Anacleto
Eber Castro Correa
Maria Lucia V. Pimentel
Gutemberg Augusto C. Santos
spellingShingle Yara Dadalti Fragoso
Heloisa Helena Ruocco
Ronaldo Maciel Dias
Hideraldo Cabeça
Ricardo Gonçalves
Nise A. de Carvalho Sousa
Caroline Vieira Spessotto
Carlos Bernardo Tauil
Soniza Vieira Alves-Leon
Sidney Gomes
Marcus Vinicius M. Gonçalves
Suzana C. Nunes Machado
Andrea Anacleto
Eber Castro Correa
Maria Lucia V. Pimentel
Gutemberg Augusto C. Santos
Late Onset of Neuromyelitis Optica Spectrum Disorders
Neurology and Therapy
Elderly
Disability
Neurology
Neuromyelitis optica
Neuromyelitis optica spectrum disorders
author_facet Yara Dadalti Fragoso
Heloisa Helena Ruocco
Ronaldo Maciel Dias
Hideraldo Cabeça
Ricardo Gonçalves
Nise A. de Carvalho Sousa
Caroline Vieira Spessotto
Carlos Bernardo Tauil
Soniza Vieira Alves-Leon
Sidney Gomes
Marcus Vinicius M. Gonçalves
Suzana C. Nunes Machado
Andrea Anacleto
Eber Castro Correa
Maria Lucia V. Pimentel
Gutemberg Augusto C. Santos
author_sort Yara Dadalti Fragoso
title Late Onset of Neuromyelitis Optica Spectrum Disorders
title_short Late Onset of Neuromyelitis Optica Spectrum Disorders
title_full Late Onset of Neuromyelitis Optica Spectrum Disorders
title_fullStr Late Onset of Neuromyelitis Optica Spectrum Disorders
title_full_unstemmed Late Onset of Neuromyelitis Optica Spectrum Disorders
title_sort late onset of neuromyelitis optica spectrum disorders
publisher Adis, Springer Healthcare
series Neurology and Therapy
issn 2193-8253
2193-6536
publishDate 2019-07-01
description Abstract Introduction Neuromyelitis optica spectrum disorder (NMOSD) is an autoimmune demyelinating disease of the central nervous system. NMOSD starting after the age of 50 years is considered a “late onset” (LO-NMOSD) and seems to be particularly aggressive. The objective of this paper is to present a series of 37 Brazilian patients with LO-NMOSD. Methods Retrospective data collection from medical records of patients with LO-NMOSD seen at 14 Brazilian specialized units. Results The ratio of women to men in the sample was 4.3 to 1. The patients were followed up for a median period of 4 years. Sex, age at disease onset, and ethnic background were not associated with the number of relapses or disability outcomes. Extensive longitudinal myelitis affected 86% of patients, while optic neuritis affected 70%, and brainstem syndromes were present in only 16% of these patients. Six patients are currently using some type of support for walking or are wheelchair-bound. Three have died. Therapeutic options for NMOSD were particularly complicated for these elderly patients, since medications for controlling NMOSD are, in essence, immunosuppressive. Long-term use of corticosteroids can be an issue when the patients have high blood pressure, diabetes mellitus, or dyslipidemia (conditions often seen in elderly individuals). Conclusion This series of LO-NMOSD cases highlights the importance of prompt diagnosis and treatment for these patients.
topic Elderly
Disability
Neurology
Neuromyelitis optica
Neuromyelitis optica spectrum disorders
url http://link.springer.com/article/10.1007/s40120-019-0143-2
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