Pediatric Multiple Sclerosis in Portugal: A Multicentre Study

Detalhes bibliográficos
Autor(a) principal: Correia, Ana Sofia
Data de Publicação: 2016
Outros Autores: Augusto, Luís, Meireles, Joana, Pinto, Joana, Sousa, Ana Paula
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6346
Resumo: Introduction: Multiple sclerosis is most often diagnosed among young adults but less frequently it may present during childhood or adolescence. In Portugal, there has been only one previous single-center, pediatric multiple sclerosis study. The main objective was the evaluation of the demographic, clinical, laboratorial and neuroradiological characteristics of patients with pediatric-onset multiple sclerosis in Portugal. The secondary objectives were to compare the characteristics of childhood-onset multiple sclerosis and adolescent-onset multiple sclerosis and to characterize the treatments prescribed.Material and Methods: We performed a retrospective observational, multicentric study. We reviewed data of all patients with multiple sclerosis younger than 18 years at the onset of their first multiple sclerosis symptoms.Results: There were 46 patients (72% female) included with a mean age at diagnosis of 16.1 years. Six cases had childhood-onset and 40 cases had adolescence-onset. The median value of Expanded Disability Status Scale was two. Relapsing-remitting multiple sclerosis was most prevalent (98% of cases). In the cerebrospinal fluid study, 74% of patients had positive oligoclonal bands. Brain magnetic resonance imaging studies showed a predominant supratentorial involvement (98% of cases), whereas the cervical segment was the most frequently affected in the spinal cord. All the patients enrolled in the study underwent immunomodulatory therapy, 75% ofpatients with beta-interferon. Concerning differences between the childhood and the adolescent groups, we found a greater proportion of male patients and of individuals with cerebrospinal fluid pleocytosis among the childhood-onset group.Discussion: This study provides new data on pediatric multiple sclerosis characteristics in Portugal and our results are similar to previously reported data in other parts of the worldConclusion: This is the first multicentric study characterizing pediatric multiple sclerosis in Portugal. The mechanisms underlying the particularities of pediatric multiple sclerosis remain largely unknown and further studies are required.
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spelling Pediatric Multiple Sclerosis in Portugal: A Multicentre StudyEsclerose Múltipla Pediátrica em Portugal: Um Estudo MulticêntricoAdolescentChildMultiple SclerosisPortugal.AdolescenteCriançaEsclerose MúltiplaPortugal.Introduction: Multiple sclerosis is most often diagnosed among young adults but less frequently it may present during childhood or adolescence. In Portugal, there has been only one previous single-center, pediatric multiple sclerosis study. The main objective was the evaluation of the demographic, clinical, laboratorial and neuroradiological characteristics of patients with pediatric-onset multiple sclerosis in Portugal. The secondary objectives were to compare the characteristics of childhood-onset multiple sclerosis and adolescent-onset multiple sclerosis and to characterize the treatments prescribed.Material and Methods: We performed a retrospective observational, multicentric study. We reviewed data of all patients with multiple sclerosis younger than 18 years at the onset of their first multiple sclerosis symptoms.Results: There were 46 patients (72% female) included with a mean age at diagnosis of 16.1 years. Six cases had childhood-onset and 40 cases had adolescence-onset. The median value of Expanded Disability Status Scale was two. Relapsing-remitting multiple sclerosis was most prevalent (98% of cases). In the cerebrospinal fluid study, 74% of patients had positive oligoclonal bands. Brain magnetic resonance imaging studies showed a predominant supratentorial involvement (98% of cases), whereas the cervical segment was the most frequently affected in the spinal cord. All the patients enrolled in the study underwent immunomodulatory therapy, 75% ofpatients with beta-interferon. Concerning differences between the childhood and the adolescent groups, we found a greater proportion of male patients and of individuals with cerebrospinal fluid pleocytosis among the childhood-onset group.Discussion: This study provides new data on pediatric multiple sclerosis characteristics in Portugal and our results are similar to previously reported data in other parts of the worldConclusion: This is the first multicentric study characterizing pediatric multiple sclerosis in Portugal. The mechanisms underlying the particularities of pediatric multiple sclerosis remain largely unknown and further studies are required.Introdução: A esclerose múltipla é habitualmente diagnosticada em adultos jovens mas, mais raramente, pode manifestar-se durante a infância ou adolescência. Os dados sobre a esclerose múltipla pediátrica em Portugal são escassos. O objectivo principal deste estudo é a avaliação das características demográficas, clínicas, laboratoriais e neurorradiológicas da esclerose múltipla de início em idade pediátrica em Portugal. Os objetivos secundários consistem na comparação entre a esclerose múltipla de início na infância e aesclerose múltipla de início na adolescência e na caracterização dos tratamentos prescritos.Material e Métodos: Realizou-se um estudo retrospectivo, observacional e multicêntrico, que consistiu na análise dos dados de todos os doentes com apresentação da EM antes dos 18 anos.Resultados: Incluíram-se 46 doentes (72% do sexo feminino), com uma idade média de diagnóstico de 16,1 anos. Seis casos tiveram início na infância, 40 na adolescência. A esclerose múltipla apresentou-se em 98% dos casos com a forma surto-remissão. O estudo do líquor revelou bandas oligoclonais em 74% dos doentes. A ressonância magnética encefálica mostrou predominantemente lesões supratentoriais (98% dos casos), enquanto que a ressonância medular revelou que o segmento cervical foi o mais frequentemente afectado. Todos os doentes iniciaram terapêutica imunomoduladora (75% com interferão β). Relativamente às diferenças entre os dois grupos etários, encontrámos uma maior proporção de doentes do sexo masculino e com pleocitose no grupo com apresentação nainfância.Discussão: Este trabalho fornece novos dados sobre as características da esclerose múltipla pediátrica em Portugal e os resultados são semelhantes aos reportados em outras partes do mundo.Conclusão: Este é o primeiro estudo multicêntrico português sobre a esclerose múltipla com apresentação na infância e adolescência. Mais estudos são necessários para clarificar os mecanismos subjacentes às particularidades da esclerose múltipla pediátrica.Ordem dos Médicos2016-08-31info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfapplication/mswordapplication/mswordapplication/pdfapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6346oai:ojs.www.actamedicaportuguesa.com:article/6346Acta Médica Portuguesa; Vol. 29 No. 7-8 (2016): July-August; 425-431Acta Médica Portuguesa; Vol. 29 N.º 7-8 (2016): Julho-Agosto; 425-4311646-07580870-399Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6346https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6346/4727https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6346/7769https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6346/7920https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6346/8009https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6346/8054Direitos de Autor (c) 2016 Acta Médica Portuguesainfo:eu-repo/semantics/openAccessCorreia, Ana SofiaAugusto, LuísMeireles, JoanaPinto, JoanaSousa, Ana Paula2022-12-20T11:04:49Zoai:ojs.www.actamedicaportuguesa.com:article/6346Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:19:17.844231Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Pediatric Multiple Sclerosis in Portugal: A Multicentre Study
Esclerose Múltipla Pediátrica em Portugal: Um Estudo Multicêntrico
title Pediatric Multiple Sclerosis in Portugal: A Multicentre Study
spellingShingle Pediatric Multiple Sclerosis in Portugal: A Multicentre Study
Correia, Ana Sofia
Adolescent
Child
Multiple Sclerosis
Portugal.
Adolescente
Criança
Esclerose Múltipla
Portugal.
title_short Pediatric Multiple Sclerosis in Portugal: A Multicentre Study
title_full Pediatric Multiple Sclerosis in Portugal: A Multicentre Study
title_fullStr Pediatric Multiple Sclerosis in Portugal: A Multicentre Study
title_full_unstemmed Pediatric Multiple Sclerosis in Portugal: A Multicentre Study
title_sort Pediatric Multiple Sclerosis in Portugal: A Multicentre Study
author Correia, Ana Sofia
author_facet Correia, Ana Sofia
Augusto, Luís
Meireles, Joana
Pinto, Joana
Sousa, Ana Paula
author_role author
author2 Augusto, Luís
Meireles, Joana
Pinto, Joana
Sousa, Ana Paula
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Correia, Ana Sofia
Augusto, Luís
Meireles, Joana
Pinto, Joana
Sousa, Ana Paula
dc.subject.por.fl_str_mv Adolescent
Child
Multiple Sclerosis
Portugal.
Adolescente
Criança
Esclerose Múltipla
Portugal.
topic Adolescent
Child
Multiple Sclerosis
Portugal.
Adolescente
Criança
Esclerose Múltipla
Portugal.
description Introduction: Multiple sclerosis is most often diagnosed among young adults but less frequently it may present during childhood or adolescence. In Portugal, there has been only one previous single-center, pediatric multiple sclerosis study. The main objective was the evaluation of the demographic, clinical, laboratorial and neuroradiological characteristics of patients with pediatric-onset multiple sclerosis in Portugal. The secondary objectives were to compare the characteristics of childhood-onset multiple sclerosis and adolescent-onset multiple sclerosis and to characterize the treatments prescribed.Material and Methods: We performed a retrospective observational, multicentric study. We reviewed data of all patients with multiple sclerosis younger than 18 years at the onset of their first multiple sclerosis symptoms.Results: There were 46 patients (72% female) included with a mean age at diagnosis of 16.1 years. Six cases had childhood-onset and 40 cases had adolescence-onset. The median value of Expanded Disability Status Scale was two. Relapsing-remitting multiple sclerosis was most prevalent (98% of cases). In the cerebrospinal fluid study, 74% of patients had positive oligoclonal bands. Brain magnetic resonance imaging studies showed a predominant supratentorial involvement (98% of cases), whereas the cervical segment was the most frequently affected in the spinal cord. All the patients enrolled in the study underwent immunomodulatory therapy, 75% ofpatients with beta-interferon. Concerning differences between the childhood and the adolescent groups, we found a greater proportion of male patients and of individuals with cerebrospinal fluid pleocytosis among the childhood-onset group.Discussion: This study provides new data on pediatric multiple sclerosis characteristics in Portugal and our results are similar to previously reported data in other parts of the worldConclusion: This is the first multicentric study characterizing pediatric multiple sclerosis in Portugal. The mechanisms underlying the particularities of pediatric multiple sclerosis remain largely unknown and further studies are required.
publishDate 2016
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dc.publisher.none.fl_str_mv Ordem dos Médicos
publisher.none.fl_str_mv Ordem dos Médicos
dc.source.none.fl_str_mv Acta Médica Portuguesa; Vol. 29 No. 7-8 (2016): July-August; 425-431
Acta Médica Portuguesa; Vol. 29 N.º 7-8 (2016): Julho-Agosto; 425-431
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