Clinical consequences of MRI activity in treated multiple sclerosis

被引:11
作者
Cadavid, Diego [1 ]
Kim, Soyeon [3 ]
Peng, Bo [3 ]
Skurnick, Joan [3 ]
Younes, Maha [1 ,4 ]
Hill, James [4 ]
Wolansky, Leo J. [2 ]
Cook, Stuart D. [1 ]
机构
[1] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Neurol & Neurosci, Newark, NJ 07103 USA
[2] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Radiol, Newark, NJ 07103 USA
[3] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Prevent Med & Community Hlth, Newark, NJ 07103 USA
[4] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Psychiat, Newark, NJ 07103 USA
关键词
Disability; glatiramer acetate; interferon beta-1b; MRI; multiple sclerosis; DISABILITY STATUS SCALE; FUNCTIONAL COMPOSITE; INTERFERON-BETA; OUTCOME MEASURE; METAANALYTIC APPROACH; MS PATIENTS; BRAIN MRI; FOLLOW-UP; LESIONS; EDSS;
D O I
10.1177/1352458511405375
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Inflammation on brain MRI is the most sensitive marker of disease activity in multiple sclerosis ( MS) but its clinical consequences remain controversial. Objective: Here we investigated the clinical consequences of MRI activity in MS subjects treated with two different first line disease modifying agents. Methods: Seventy-five treatment-naive subjects with relapsing-remitting MS (N = 61) or clinically isolated syndromes at risk of MS (N = 14) from the BECOME study that had been randomized to interferon beta-1b (N = 39) or glatiramer acetate (N = 36) and followed for up to two years by monthly brain MRI optimized to detect inflammatory activity were studied for the clinical consequences of lack of MRI remission. Results: MRI remission occurred in 46.4% of participants transiently and in 23.2% completely while it was never achieved in 30.4%. There was no difference by treatment in MRI remission, progression of physical disability, or cognitive function. The percentage of relapse-free subjects was 87.5% for the group in complete MRI remission, 47.6% in the group never in remission and 59.4% in the group in transient remission (p = 0.017). Similar differences were observed for six-month-confirmed worsening of ambulatory function as measured by the timed 25 foot walk (p = 0.026) and by Expanded Disability Status Scale (EDSS) (p = 0.10). Cognitive function was lowest at baseline for the group that never reached MRI remission on treatment; this group improved the least upon repeated cognitive testing during the two years of treatment (p < 0.001). Conclusions: Lack of MRI remission during treatment with interferon beta-1b or glatiramer acetate is associated with higher relapse rate and worsening of physical and cognitive function.
引用
收藏
页码:1113 / 1121
页数:9
相关论文
共 33 条
[1]   QUANTITATIVE MRI CHANGES IN GADOLINIUM-DTPA ENHANCEMENT AFTER HIGH-DOSE INTRAVENOUS METHYLPREDNISOLONE IN MULTIPLE-SCLEROSIS [J].
BARKHOF, F ;
HOMMES, OR ;
SCHELTENS, P ;
VALK, J .
NEUROLOGY, 1991, 41 (08) :1219-1222
[2]   MRI in multiple sclerosis: correlation with expanded disability status scale (EDSS) [J].
Barkhof, F .
MULTIPLE SCLEROSIS JOURNAL, 1999, 5 (04) :283-286
[3]   Minimal neuropsychological assessment of MS patients: A consensus approach [J].
Benedict, RHB ;
Fischer, JS ;
Archibald, CJ ;
Arnett, PA ;
Beatty, WW ;
Bobholz, J ;
Chelune, GJ ;
Fisk, JD ;
Langdon, DW ;
Caruso, L ;
Foley, F ;
LaRocca, NG ;
Vowels, L ;
Weinstein, A ;
DeLuca, J ;
Rao, SM ;
Munschauer, F .
CLINICAL NEUROPSYCHOLOGIST, 2002, 16 (03) :381-397
[4]   New acute and chronic black holes in patients with multiple sclerosis randomised to interferon beta-1b or glatiramer acetate [J].
Cadavid, D. ;
Cheriyan, J. ;
Skurnick, J. ;
Lincoln, J. A. ;
Wolansky, L. J. ;
Cook, S. D. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2009, 80 (12) :1337-1343
[5]   Efficacy of treatment of MS with IFNβ-1b or glatiramer acetate by monthly brain MRI in the BECOME study [J].
Cadavid, D. ;
Wolansky, L. J. ;
Skurnick, J. ;
Lincoln, J. ;
Cheriyan, J. ;
Szczepanowski, K. ;
Kamin, S. S. ;
Pachner, A. R. ;
Halper, J. ;
Cook, S. D. .
NEUROLOGY, 2009, 72 (23) :1976-1983
[6]   Responsiveness of the Expanded Disability Status Scale (EDSS) to disease progression and therapeutic intervention in progressive forms of multiple sclerosis [J].
Cadavid, Diego ;
Tang, Yongqiang ;
O'Neill, Gilmore .
REVISTA DE NEUROLOGIA, 2010, 51 (06) :321-329
[7]   Development of a multiple sclerosis functional composite as a clinical trial outcome measure [J].
Cutter, GR ;
Baier, ML ;
Rudick, RA ;
Cookfair, DL ;
Fischer, JS ;
Petkau, J ;
Syndulko, K ;
Weinshenker, BG ;
Antel, JP ;
Confavreux, C ;
Ellison, GW ;
Lublin, F ;
Miller, AE ;
Rao, SM ;
Reingold, S ;
Thompson, A ;
Willoughby, E .
BRAIN, 1999, 122 :871-882
[8]   MRI as an outcome in multiple sclerosis clinical trials [J].
Daumer, M. ;
Neuhaus, A. ;
Morrissey, S. ;
Hintzen, R. ;
Ebers, G. C. .
NEUROLOGY, 2009, 72 (08) :705-711
[9]   MRI activity and neutralising antibody as predictors of response to interferon β treatment in multiple sclerosis [J].
Durelli, L. ;
Barbero, P. ;
Bergui, M. ;
Versino, E. ;
Bassano, M. A. ;
Verdun, E. ;
Rivoiro, C. ;
Ferrero, C. ;
Picco, E. ;
Ripellino, P. ;
Giuliani, G. ;
Montanari, E. ;
Clerico, M. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2008, 79 (06) :646-651
[10]   Disability as an outcome in MS clinical trials [J].
Ebers, G. C. ;
Heigenhauser, L. ;
Daumer, M. ;
Lederer, C. ;
Noseworthy, J. H. .
NEUROLOGY, 2008, 71 (09) :624-631