Defining the clinical course of multiple sclerosis
By F. Lublin, S. Reingold, Jeffrey A. Cohen, G. Cutter, P. Sørensen, Alan J. Thompson, J. Wolinsky, L. Balcer, B. Banwell, Frederik Barkhof and 22 more. Neurology, 2014
2,587 citations recorded by the source corpus.
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.
Subfields: Oncology, Pathology and Forensic Medicine, Rheumatology
View Paper: https://www.semanticscholar.org/paper/cee4c00ef8816059c5a7270d31745ecf808d68e3
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In Pathology and Forensic Medicine
Citations in the corpus
- Placebo-controlled phase 3 study of oral BG-12 or glatiramer in multiple sclerosis. (2012, neutral): “Multiple sclerosis relapse 51 (14) 39 (11) 30 (9) 36 (10)”
- Multiple sclerosis – a review (2018, positive): “Given the above, MS can be thought of as a single disease existing within a spectrum extending from relapsing (‘inflammatory dominant’) to progressive (‘neurodegeneration dominant’), in keeping with the 2013 revisions to the clinical course of MS [48].”