Ten-year follow-up of the 'minimal MRI lesion' subgroup from the original CHAMPS Multiple Sclerosis Prevention Trial

被引:11
|
作者
Simon, J. H. [1 ,2 ]
Kinkel, R. P. [3 ]
Kollman, C. [4 ]
O'Connor, P. [5 ]
Fisher, E. [6 ]
You, X. [7 ]
Hyde, R. [8 ]
机构
[1] Portland VA Med Ctr, VA Med Ctr, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Portland, OR 97239 USA
[3] Univ Calif San Diego, Dept Neurosci, La Jolla, CA 92093 USA
[4] Jaeb Ctr Hlth Res, Dept Biostat, Tampa, FL USA
[5] St Michaels Hosp, Multiple Sclerosis Clin, Toronto, ON M5B 1W8, Canada
[6] Cleveland Clin, Dept Biomed Engn, Cleveland, OH 44106 USA
[7] Biogen Idec Inc, Dept Biostat, Cambridge, MA USA
[8] Biogen Idec Inc, Global Med Affairs, Cambridge, MA USA
关键词
CHAMPS; CHAMPIONS; disease progression; intramuscular interferon beta-1a; MRI; multiple sclerosis; clinically isolated syndrome; CLINICALLY ISOLATED SYNDROMES; INTRAMUSCULAR INTERFERON BETA-1A; 1ST DEMYELINATING EVENT; DISABILITY; DEFINITE; MS; CONVERSION;
D O I
10.1177/1352458514547407
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Patients with clinically isolated syndrome (CIS) and characteristic magnetic resonance imaging (MRI) lesions are at high risk for multiple sclerosis (MS). However, patients with a minimal MRI lesion burden (a low T2-hyperintense [low T2] lesion count) may have borderline formal diagnostic criteria, presenting a clinical management challenge. Objective: Compare the 10-year disease progression of patients with low and higher T2 lesion counts treated over most intervals. Methods: CIS patients from the original CHAMPS MS trial were retrospectively assigned to low-T2 (first quartile; 2-8 lesions) or higher-T2 (second through fourth quartiles; 9 lesions) groups using baseline T2 lesion counts. The 5- and 10-year open-label extension of CHAMPS (CHAMPIONS) evaluated conversion to clinically definite MS (CDMS), MRI activity, relapses, and disability. Results: The vast majority of patients showed new disease activity by MRI and/or clinical criteria at 10 years (low-T2 86%; higher-T2 98%). Fewer low-T2 than higher-T2 patients developed CDMS (40% vs. 63%; p = 0.013); low-T2 patients also had fewer new brain lesions, less brain volume loss, and less disability progression. Conclusion: CIS patients with low T2 lesion counts show continued disease activity. However, all assessments of disease progression over 10 years indicated a significantly less severe disease course for low-T2 patients.
引用
收藏
页码:415 / 422
页数:8
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