Ten-year follow-up of the 'minimal MRI lesion' subgroup from the original CHAMPS Multiple Sclerosis Prevention Trial
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作者:
Simon, J. H.
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Portland VA Med Ctr, VA Med Ctr, Portland, OR 97239 USA
Oregon Hlth & Sci Univ, Portland, OR 97239 USAPortland VA Med Ctr, VA Med Ctr, Portland, OR 97239 USA
Simon, J. H.
[1
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Kinkel, R. P.
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Univ Calif San Diego, Dept Neurosci, La Jolla, CA 92093 USAPortland VA Med Ctr, VA Med Ctr, Portland, OR 97239 USA
Kinkel, R. P.
[3
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Kollman, C.
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Jaeb Ctr Hlth Res, Dept Biostat, Tampa, FL USAPortland VA Med Ctr, VA Med Ctr, Portland, OR 97239 USA
Kollman, C.
[4
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O'Connor, P.
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St Michaels Hosp, Multiple Sclerosis Clin, Toronto, ON M5B 1W8, CanadaPortland VA Med Ctr, VA Med Ctr, Portland, OR 97239 USA
O'Connor, P.
[5
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Fisher, E.
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Cleveland Clin, Dept Biomed Engn, Cleveland, OH 44106 USAPortland VA Med Ctr, VA Med Ctr, Portland, OR 97239 USA
Fisher, E.
[6
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You, X.
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Biogen Idec Inc, Dept Biostat, Cambridge, MA USAPortland VA Med Ctr, VA Med Ctr, Portland, OR 97239 USA
You, X.
[7
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Hyde, R.
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Biogen Idec Inc, Global Med Affairs, Cambridge, MA USAPortland VA Med Ctr, VA Med Ctr, Portland, OR 97239 USA
Hyde, R.
[8
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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
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.
机构:
St Lukes Int Hosp, Dept Ophthalmol, Chuo Ku, Tokyo 1048560, Japan
Juntendo Univ, Dept Ophthalmol, Urayasu Hosp, Urayasu, Chiba 2790021, JapanSt Lukes Int Hosp, Dept Ophthalmol, Chuo Ku, Tokyo 1048560, Japan
Koshimizu, Junko
Dhanuka, Raksha
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St Lukes Int Hosp, Dept Ophthalmol, Chuo Ku, Tokyo 1048560, JapanSt Lukes Int Hosp, Dept Ophthalmol, Chuo Ku, Tokyo 1048560, Japan
Dhanuka, Raksha
Yamaguchi, Tatsuo
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St Lukes Int Hosp, Dept Ophthalmol, Chuo Ku, Tokyo 1048560, JapanSt Lukes Int Hosp, Dept Ophthalmol, Chuo Ku, Tokyo 1048560, Japan