Literature DB >> 17582070

Natural history of multiple sclerosis with childhood onset.

Christel Renoux1, Sandra Vukusic, Yann Mikaeloff, Gilles Edan, Michel Clanet, Bénédicte Dubois, Marc Debouverie, Bruno Brochet, Christine Lebrun-Frenay, Jean Pelletier, Thibault Moreau, Catherine Lubetzki, Patrick Vermersch, Etienne Roullet, Laurent Magy, Marc Tardieu, Samy Suissa, Christian Confavreux.   

Abstract

BACKGROUND: The course and prognosis of childhood-onset multiple sclerosis have not been well described.
METHODS: We used data from 13 adult neurology departments affiliated with the European Database for Multiple Sclerosis (EDMUS) network to identify a cohort of 394 patients who had multiple sclerosis with an onset at 16 years of age or younger and a comparison group of 1775 patients who had multiple sclerosis with an onset after 16 years of age. We determined the initial clinical features, the dates of disease onset, and the occurrence of outcomes, including relapse, conversion to secondary progression, and irreversible disability as measured by scores of 4 (limited walking ability but ability to walk more than 500 m without aid or rest), 6 (ability to walk with unilateral support no more than 100 m without rest), and 7 (ability to walk no more than 10 m without rest while using a wall or furniture for support) on the Kurtzke Disability Status Scale (range, 0 to 10; higher scores indicate more severe disability).
RESULTS: For patients with childhood-onset multiple sclerosis, the estimated median time from onset to secondary progression was 28 years, and the median age at conversion to secondary progression was 41 years. The median times from onset to disability scores of 4, 6, and 7 were 20.0, 28.9, and 37.0 years, respectively, and the corresponding median ages were 34.6, 42.2, and 50.5 years. In comparison with patients with adult-onset disease, those with childhood-onset disease were more likely to be female than male (female:male ratio, 2.8 vs. 1.8), were more likely to have an exacerbating-remitting initial course (98% vs. 84%), took approximately 10 years longer to reach secondary progression and irreversible disability, and reached these landmarks at an age approximately 10 years younger (P<0.001 for all comparisons).
CONCLUSIONS: Patients with childhood-onset multiple sclerosis take longer to reach states of irreversible disability but do so at a younger age than patients with adult-onset multiple sclerosis.

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Mesh:

Year:  2007        PMID: 17582070     DOI: 10.1056/NEJMoa067597

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


  126 in total

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Authors:  Hasan A Al-Hamadani; Atheer S Abdalla; Atheer J Al-Saffar
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2.  Magnetic resonance imaging features of the spinal cord in pediatric multiple sclerosis: a preliminary study.

Authors:  Leonard H Verhey; Helen M Branson; Monica Makhija; Manohar Shroff; Brenda Banwell
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7.  Characteristics of Children and Adolescents With Multiple Sclerosis.

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Review 8.  Pediatric multiple sclerosis.

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Review 9.  Disease-modifying therapy of pediatric multiple sclerosis.

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Review 10.  Therapeutic Approach to the Management of Pediatric Demyelinating Disease: Multiple Sclerosis and Acute Disseminated Encephalomyelitis.

Authors:  J Nicholas Brenton; Brenda L Banwell
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