Relationship between brain atrophy and disability: an 8-year follow-up study of multiple sclerosis patients

被引:127
作者
Fisher, E [1 ]
Rudick, RA
Cutter, G
Baier, M
Miller, D
Weinstock-Guttman, B
Mass, MK
Dougherty, DS
Simonian, NA
机构
[1] Cleveland Clin Fdn, Dept Biomed Engn ND20, Cleveland, OH 44195 USA
[2] Cleveland Clin Fdn, Dept Neurol, Mellen Ctr, Cleveland, OH 44195 USA
[3] AMC, Ctr Canc Res, Ctr Res Methodol & Biometr, Lakewood, CO 80214 USA
[4] Buffalo Gen Hosp, Dept Neurol, Buffalo, NY 14203 USA
[5] Oregon Hlth Sci Univ, Dept Neurol, Portland, OR 97201 USA
[6] Walter Reed Army Med Ctr, DVHIP, Washington, DC 20307 USA
[7] Biogen Inc, Boston, MA 02142 USA
来源
MULTIPLE SCLEROSIS | 2000年 / 6卷 / 06期
关键词
multiple sclerosis; magnetic resonance imaging; brain atrophy;
D O I
10.1191/135245800701566331
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Brain atrophy measurement con Provide an estimate of the amount of tissue destruction due to the pathologic processes in multiple sclerosis. The potential usefulness of atrophy as a marker of disease progression depends upon the concurrent and predictive relationships between atrophy and disability A follow-up study was Performed to measure atrophy and disability scores in patients from the Multiple Sclerosis Collaborative Research Group's phase III trial of IFN beta -1a (Avonex) in relapsing-remitting multiple sclerosis. New data were obtained on 160 out of 172 eligible patients from the original trial were enrolled in the follow-up study approximately 8 years after randomization. The follow-up visit consisted of several tests and questionnaires including a clinical exam to determine Expanded Disability Status Score (EDSS) and Multiple Sclerosis Functional Composite (MSFC), and a magnetic resonance imaging exam to calculate the brain parenchymal faction. Brain parenchymal fraction was correlated with both EDSS and MSFC at each of the four time Points for which data were available (baseline 1, 2 and 8 years). Furthermore, the change in BPF was correlated with the changes in disability scores from the end of the phase III trial to the follow-vp exam. These data suggest that brain atrophy may be a useful and clinically relevant marker of disease Progression in relapsing-remitting MS.
引用
收藏
页码:373 / 377
页数:5
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