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Response to Interferon-Beta Treatment in Afro-Caribbeans with Multiple Sclerosis

Background. Multiple sclerosis (MS) patients of African ancestry have a more aggressive disease course than white patients and could be resistant to interferon-beta (INFB). Methods. We studied the impact of INFB in treatment-naive Afro-Caribbean (AC) with clinically definite MS using our European Da...

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Detalles Bibliográficos
Autores principales: Jeannin, S., Deschamps, R., Chausson, N., Cabre, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195322/
https://www.ncbi.nlm.nih.gov/pubmed/22096646
http://dx.doi.org/10.1155/2011/950126
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author Jeannin, S.
Deschamps, R.
Chausson, N.
Cabre, P.
author_facet Jeannin, S.
Deschamps, R.
Chausson, N.
Cabre, P.
author_sort Jeannin, S.
collection PubMed
description Background. Multiple sclerosis (MS) patients of African ancestry have a more aggressive disease course than white patients and could be resistant to interferon-beta (INFB). Methods. We studied the impact of INFB in treatment-naive Afro-Caribbean (AC) with clinically definite MS using our European Database for Multiple Sclerosis (EDMUS) (2003–2010). Main outcome measures were annual relapse rate after 2 years of treatment, proportion of exacerbation-free subjects 48 weeks after initiating INFB, and time to first relapse. Results. 76 AC-MS (59F/17M) were identified. Annual relapse rate of 1.29 decreased to 0.83 (−35.6%) after 2 years of treatment. The proportion of relapse-free patients at 48 weeks was 46.2%. Median time to first relapse was 52 weeks. Conclusion. INFB is not strong enough to control AC-MS patients in many cases which is problematic in a population of worse MS prognosis.
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spelling pubmed-31953222011-11-17 Response to Interferon-Beta Treatment in Afro-Caribbeans with Multiple Sclerosis Jeannin, S. Deschamps, R. Chausson, N. Cabre, P. Mult Scler Int Clinical Study Background. Multiple sclerosis (MS) patients of African ancestry have a more aggressive disease course than white patients and could be resistant to interferon-beta (INFB). Methods. We studied the impact of INFB in treatment-naive Afro-Caribbean (AC) with clinically definite MS using our European Database for Multiple Sclerosis (EDMUS) (2003–2010). Main outcome measures were annual relapse rate after 2 years of treatment, proportion of exacerbation-free subjects 48 weeks after initiating INFB, and time to first relapse. Results. 76 AC-MS (59F/17M) were identified. Annual relapse rate of 1.29 decreased to 0.83 (−35.6%) after 2 years of treatment. The proportion of relapse-free patients at 48 weeks was 46.2%. Median time to first relapse was 52 weeks. Conclusion. INFB is not strong enough to control AC-MS patients in many cases which is problematic in a population of worse MS prognosis. Hindawi Publishing Corporation 2011 2011-05-23 /pmc/articles/PMC3195322/ /pubmed/22096646 http://dx.doi.org/10.1155/2011/950126 Text en Copyright © 2011 S. Jeannin et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Jeannin, S.
Deschamps, R.
Chausson, N.
Cabre, P.
Response to Interferon-Beta Treatment in Afro-Caribbeans with Multiple Sclerosis
title Response to Interferon-Beta Treatment in Afro-Caribbeans with Multiple Sclerosis
title_full Response to Interferon-Beta Treatment in Afro-Caribbeans with Multiple Sclerosis
title_fullStr Response to Interferon-Beta Treatment in Afro-Caribbeans with Multiple Sclerosis
title_full_unstemmed Response to Interferon-Beta Treatment in Afro-Caribbeans with Multiple Sclerosis
title_short Response to Interferon-Beta Treatment in Afro-Caribbeans with Multiple Sclerosis
title_sort response to interferon-beta treatment in afro-caribbeans with multiple sclerosis
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195322/
https://www.ncbi.nlm.nih.gov/pubmed/22096646
http://dx.doi.org/10.1155/2011/950126
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