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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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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