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Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study
Acquired demyelinating syndromes (ADS) can be a first presentation of multiple sclerosis (MS) in children. The incidence of these disorders in Europe is currently unknown. Children (<18 years old) living in the Netherlands who presented with ADS were included from January 1, 2007 to December 31,...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3432787/ https://www.ncbi.nlm.nih.gov/pubmed/22349866 http://dx.doi.org/10.1007/s00415-012-6441-6 |
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author | Ketelslegers, I. A. Catsman-Berrevoets, C. E. Neuteboom, R. F. Boon, M. van Dijk, K. G. J. Eikelenboom, M. J. Gooskens, R. H. J. M. Niks, E. H. Overweg-Plandsoen, W. C. G. Peeters, E. A. J. Peeters-Scholte, C. M. P. C. D. Poll-The, B. T. de Rijk-van Andel, J. F. Samijn, J. P. A. Snoeck, I. N. Stroink, H. Vermeulen, R. J. Verrips, A. Vles, J. S. H. Willemsen, M. A. A. P. Rodrigues Pereira, R. Hintzen, R. Q. |
author_facet | Ketelslegers, I. A. Catsman-Berrevoets, C. E. Neuteboom, R. F. Boon, M. van Dijk, K. G. J. Eikelenboom, M. J. Gooskens, R. H. J. M. Niks, E. H. Overweg-Plandsoen, W. C. G. Peeters, E. A. J. Peeters-Scholte, C. M. P. C. D. Poll-The, B. T. de Rijk-van Andel, J. F. Samijn, J. P. A. Snoeck, I. N. Stroink, H. Vermeulen, R. J. Verrips, A. Vles, J. S. H. Willemsen, M. A. A. P. Rodrigues Pereira, R. Hintzen, R. Q. |
author_sort | Ketelslegers, I. A. |
collection | PubMed |
description | Acquired demyelinating syndromes (ADS) can be a first presentation of multiple sclerosis (MS) in children. The incidence of these disorders in Europe is currently unknown. Children (<18 years old) living in the Netherlands who presented with ADS were included from January 1, 2007 to December 31, 2010 by the Dutch pediatric MS study group and the Dutch surveillance of rare pediatric disorders. Demographic and clinical data were collected. Eighty-six patients were identified over 4 years, resulting in an incidence of 0.66/1,00,000 per year. Most patients presented with polyfocal ADS without encephalopathy (30%), followed by polyfocal ADS with encephalopathy (24%), optic neuritis (ON, 22%), monofocal ADS (16%), transverse myelitis (3%), and neuromyelitis optica (3%). Patients with polyfocal ADS with encephalopathy were younger (median 3.9 years) than patients with ON (median 14.6 years, p < 0.001) or monofocal ADS (median 16.0 years, p < 0.001). Patients with polyfocal ADS without encephalopathy (median 9.2 years) were also younger than monofocal ADS patients (median 16.0 years, p < 0.001). There was a slight female preponderance in all groups except the ON group, and a relatively large number of ADS patients (29%) reported a non-European ancestry. Familial autoimmune diseases were reported in 23%, more often in patients with relapsing disease than monophasic disease (46 vs. 15%, p = 0.002) and occurring most often in the maternal family (84%, p < 0.001). During the study period, 23% of patients were subsequently diagnosed with MS. The annual incidence of ADS in the Netherlands is 0.66/1,00,000 children/year. A polyfocal disease onset of ADS was most common. |
format | Online Article Text |
id | pubmed-3432787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-34327872012-09-07 Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study Ketelslegers, I. A. Catsman-Berrevoets, C. E. Neuteboom, R. F. Boon, M. van Dijk, K. G. J. Eikelenboom, M. J. Gooskens, R. H. J. M. Niks, E. H. Overweg-Plandsoen, W. C. G. Peeters, E. A. J. Peeters-Scholte, C. M. P. C. D. Poll-The, B. T. de Rijk-van Andel, J. F. Samijn, J. P. A. Snoeck, I. N. Stroink, H. Vermeulen, R. J. Verrips, A. Vles, J. S. H. Willemsen, M. A. A. P. Rodrigues Pereira, R. Hintzen, R. Q. J Neurol Original Communication Acquired demyelinating syndromes (ADS) can be a first presentation of multiple sclerosis (MS) in children. The incidence of these disorders in Europe is currently unknown. Children (<18 years old) living in the Netherlands who presented with ADS were included from January 1, 2007 to December 31, 2010 by the Dutch pediatric MS study group and the Dutch surveillance of rare pediatric disorders. Demographic and clinical data were collected. Eighty-six patients were identified over 4 years, resulting in an incidence of 0.66/1,00,000 per year. Most patients presented with polyfocal ADS without encephalopathy (30%), followed by polyfocal ADS with encephalopathy (24%), optic neuritis (ON, 22%), monofocal ADS (16%), transverse myelitis (3%), and neuromyelitis optica (3%). Patients with polyfocal ADS with encephalopathy were younger (median 3.9 years) than patients with ON (median 14.6 years, p < 0.001) or monofocal ADS (median 16.0 years, p < 0.001). Patients with polyfocal ADS without encephalopathy (median 9.2 years) were also younger than monofocal ADS patients (median 16.0 years, p < 0.001). There was a slight female preponderance in all groups except the ON group, and a relatively large number of ADS patients (29%) reported a non-European ancestry. Familial autoimmune diseases were reported in 23%, more often in patients with relapsing disease than monophasic disease (46 vs. 15%, p = 0.002) and occurring most often in the maternal family (84%, p < 0.001). During the study period, 23% of patients were subsequently diagnosed with MS. The annual incidence of ADS in the Netherlands is 0.66/1,00,000 children/year. A polyfocal disease onset of ADS was most common. Springer-Verlag 2012-02-17 2012 /pmc/articles/PMC3432787/ /pubmed/22349866 http://dx.doi.org/10.1007/s00415-012-6441-6 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Communication Ketelslegers, I. A. Catsman-Berrevoets, C. E. Neuteboom, R. F. Boon, M. van Dijk, K. G. J. Eikelenboom, M. J. Gooskens, R. H. J. M. Niks, E. H. Overweg-Plandsoen, W. C. G. Peeters, E. A. J. Peeters-Scholte, C. M. P. C. D. Poll-The, B. T. de Rijk-van Andel, J. F. Samijn, J. P. A. Snoeck, I. N. Stroink, H. Vermeulen, R. J. Verrips, A. Vles, J. S. H. Willemsen, M. A. A. P. Rodrigues Pereira, R. Hintzen, R. Q. Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study |
title | Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study |
title_full | Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study |
title_fullStr | Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study |
title_full_unstemmed | Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study |
title_short | Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study |
title_sort | incidence of acquired demyelinating syndromes of the cns in dutch children: a nationwide study |
topic | Original Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3432787/ https://www.ncbi.nlm.nih.gov/pubmed/22349866 http://dx.doi.org/10.1007/s00415-012-6441-6 |
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