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Defining the clinical course of multiple sclerosis: The 2013 revisions

Accurate clinical course descriptions (phenotypes) of multiple sclerosis (MS) are important for communication, prognostication, design and recruitment of clinical trials, and treatment decision-making. Standardized descriptions published in 1996 based on a survey of international MS experts provided...

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Detalles Bibliográficos
Autores principales: Lublin, Fred D., Reingold, Stephen C., Cohen, Jeffrey A., Cutter, Gary R., Sørensen, Per Soelberg, Thompson, Alan J., Wolinsky, Jerry S., Balcer, Laura J., Banwell, Brenda, Barkhof, Frederik, Bebo, Bruce, Calabresi, Peter A., Clanet, Michel, Comi, Giancarlo, Fox, Robert J., Freedman, Mark S., Goodman, Andrew D., Inglese, Matilde, Kappos, Ludwig, Kieseier, Bernd C., Lincoln, John A., Lubetzki, Catherine, Miller, Aaron E., Montalban, Xavier, O'Connor, Paul W., Petkau, John, Pozzilli, Carlo, Rudick, Richard A., Sormani, Maria Pia, Stüve, Olaf, Waubant, Emmanuelle, Polman, Chris H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4117366/
https://www.ncbi.nlm.nih.gov/pubmed/24871874
http://dx.doi.org/10.1212/WNL.0000000000000560
Descripción
Sumario:Accurate clinical course descriptions (phenotypes) of multiple sclerosis (MS) are important for communication, prognostication, design and recruitment of clinical trials, and treatment decision-making. Standardized descriptions published in 1996 based on a survey of international MS experts provided purely clinical phenotypes based on data and consensus at that time, but imaging and biological correlates were lacking. Increased understanding of MS and its pathology, coupled with general concern that the original descriptors may not adequately reflect more recently identified clinical aspects of the disease, prompted a re-examination of MS disease phenotypes by the International Advisory Committee on Clinical Trials of MS. While imaging and biological markers that might provide objective criteria for separating clinical phenotypes are lacking, we propose refined descriptors that include consideration of disease activity (based on clinical relapse rate and imaging findings) and disease progression. Strategies for future research to better define phenotypes are also outlined.