A longitudinal study of abnormalities on MRI and disability from multiple sclerosis

被引:625
作者
Brex, PA
Ciccarelli, O
O'Riordan, JI
Sailer, M
Thompson, AJ
Miller, DH
机构
[1] UCL Inst Neurol, NMR Res Unit, London WC1N 3BG, England
[2] Ninewells Hosp, Tayside Multiple Sclerosis Res Unit, Dundee DD1 9SY, Scotland
[3] Otto Von Guericke Univ, Magdeburg, Germany
关键词
D O I
10.1056/NEJMoa011341
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In patients with isolated syndromes that are clinically suggestive of multiple sclerosis, such as optic neuritis or brain-stem or spinal cord syndromes, the presence of lesions as determined by T(2)-weighted magnetic resonance imaging (MRI) of the brain increases the likelihood that multiple sclerosis will develop. We sought to determine the relation between early lesion volume, changes in volume, and long-term disability. Methods: Seventy-one patients in a serial MRI study of patients with isolated syndromes were reassessed after a mean of 14.1 years. Disability was measured with the use of Kurtzke's Expanded Disability Status Scale (EDSS; possible range, 0 to 10, with a higher score indicating a greater degree of disability). Results: Clinically definite multiple sclerosis developed in 44 of the 50 patients (88 percent) with abnormal results on MRI at presentation and in 4 of 21 patients (19 percent) with normal results on MRI. The median EDSS score at follow-up for those with multiple sclerosis was 3.25 (range, 0 to 10); 31 percent had an EDSS score of 6 or more (including three patients whose deaths were due to multiple sclerosis). The EDSS score at 14 years correlated moderately with lesion volume on MRI at 5 years (r=0.60) and with the increase in lesion volume over the first 5 years (r=0.61). Conclusions: In patients who first present with isolated syndromes suggestive of multiple sclerosis, the increases in the volume of the lesions seen on magnetic resonance imaging of the brain in the first five years correlate with the degree of long-term disability from multiple sclerosis. This relation is only moderate, so the volume of the lesions alone may not be an adequate basis for decisions about the use of disease-modifying treatment. (N Engl J Med 2002;346:158-64.) Copyright (C) 2002 Massachusetts Medical Society.
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页码:158 / 164
页数:7
相关论文
共 42 条
[1]  
ALTMAN DG, 1991, PRACTICAL STAT MED R, P293
[2]   Comparison of MRI criteria at first presentation to predict conversion to clinically definite multiple sclerosis [J].
Barkhof, F ;
Filippi, M ;
Miller, DH ;
Scheltens, P ;
Campi, A ;
Polman, CH ;
Comi, G ;
Ader, HJ ;
Losseff, N ;
Valk, J .
BRAIN, 1997, 120 :2059-2069
[3]  
Brodsky M, 1997, NEUROLOGY, V49, P1404
[4]   Effect of early interferon treatment on conversion to definite multiple sclerosis:: a randomised study [J].
Comi, G ;
Filippi, M ;
Barkhof, F ;
Durelli, L ;
Edan, G ;
Fernández, O ;
Hartung, HP ;
Seeldrayers, P ;
Sorensen, PS ;
Rovaris, M ;
Martinelli, V ;
Hommes, OR .
LANCET, 2001, 357 (9268) :1576-1582
[5]   Relapses and progression of disability in multiple sclerosis. [J].
Confavreux, C ;
Vukusic, S ;
Moreau, T ;
Adeleine, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (20) :1430-1438
[6]   COURSE AND PROGNOSIS OF MULTIPLE-SCLEROSIS ASSESSED BY THE COMPUTERIZED DATA-PROCESSING OF 349 PATIENTS [J].
CONFAVREUX, C ;
AIMARD, G ;
DEVIC, M .
BRAIN, 1980, 103 (JUN) :281-300
[7]  
Efron B., 1993, INTRO BOOTSTRAP, V1st ed., DOI DOI 10.1201/9780429246593
[8]   Axonal damage in acute multiple sclerosis lesions [J].
Ferguson, B ;
Matyszak, MK ;
Esiri, MM ;
Perry, VH .
BRAIN, 1997, 120 :393-399
[9]   Interscanner variation in brain MRI lesion load measurements in MS: Implications for clinical trials [J].
Filippi, M ;
vanWaesberghe, JH ;
Horsfield, MA ;
Bressi, S ;
Gasperini, C ;
Yousry, TA ;
GawneCain, ML ;
Morrissey, SP ;
Rocca, MA ;
Barkhof, F ;
Nijeholt, GJLA ;
Bastianello, S ;
Miller, DH .
NEUROLOGY, 1997, 49 (02) :371-377
[10]   A REASSESSMENT OF THE RISK OF MULTIPLE-SCLEROSIS DEVELOPING IN PATIENTS WITH OPTIC NEURITIS AFTER EXTENDED FOLLOW-UP [J].
FRANCIS, DA ;
COMPSTON, DAS ;
BATCHELOR, JR ;
MCDONALD, WI .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1987, 50 (06) :758-765