QUANTITATIVE BRAIN MRI LESION LOAD PREDICTS THE COURSE OF CLINICALLY ISOLATED SYNDROMES SUGGESTIVE OF MULTIPLE-SCLEROSIS

被引:277
作者
FILIPPI, M [1 ]
HORSFIELD, MA [1 ]
MORRISSEY, SP [1 ]
MACMANUS, DG [1 ]
RUDGE, P [1 ]
MCDONALD, WI [1 ]
MILLER, DH [1 ]
机构
[1] INST NEUROL,RES GRP,NMR,LONDON WC1N 3BG,ENGLAND
关键词
D O I
10.1212/WNL.44.4.635
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We performed semiautomated quantitative measurement of brain magnetic resonance imaging (MRI) abnormalities seen at presentation and at 5-year follow-up in 84 patients presenting with an acute clinically isolated syndrome of the optic nerves, brainstem, or spinal cord suggestive of multiple sclerosis (MS). At follow-up, 34 (40%) had developed clinically definite and four (5%) clinically probable MS. Patients who developed MS during followup had a higher lesion load at presentation than those who did not. There was a strong correlation of the MRI lesion load at presentation with both the increase in lesion load over the next 5 years and disability at follow-up. Increasing initial lesion load correlated with a decreasing time to development of MS clinically (r = -0.328, p < 0.05). At follow-up, disability and brain lesion load were strongly correlated in patients who had developed MS. These results establish that MRI at presentation with clinically isolated syndromes suggestive of MS is useful in predicting the subsequent clinical course and the development of new MRI lesions. This suggests that quantitative brain MRI will be helpful in selecting patients with early clinical MS for treatment trials and for subsequent monitoring of their response to treatment.
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页码:635 / 641
页数:7
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  • [1] Allen I V, 1981, Acta Neuropathol Suppl, V7, P176
  • [2] ATLAS SW, 1986, J COMPUT ASSIST TOMO, V8, P381
  • [3] QUANTITATIVE MULTIPLE-SCLEROSIS PLAQUE ASSESSMENT WITH MAGNETIC-RESONANCE IMAGING - ITS CORRELATION WITH CLINICAL-PARAMETERS, EVOKED-POTENTIALS, AND INTRA-BLOOD-BRAIN BARRIER IGG SYNTHESIS
    BAUMHEFNER, RW
    TOURTELLOTTE, WW
    SYNDULKO, K
    WALUCH, V
    ELLISON, GW
    MEYERS, LW
    COHEN, SN
    OSBORNE, M
    SHAPSHAK, P
    [J]. ARCHIVES OF NEUROLOGY, 1990, 47 (01) : 19 - 26
  • [4] BRANTZAWADZKI M, 1985, AM J NEURORADIOL, V6, P675
  • [5] BROMAN T, 1981, ACTA NEUROL SCAND, V63, P6
  • [6] CANAL N, 1989, MULTIPLE SCLEROSIS R, P105
  • [7] PROSPECTIVE-STUDY OF THE RISK OF DEVELOPING MULTIPLE-SCLEROSIS IN UNCOMPLICATED OPTIC NEURITIS
    COHEN, MM
    LESSEL, S
    WOLF, PA
    [J]. NEUROLOGY, 1979, 29 (02) : 208 - 213
  • [8] DUNN V, 1986, Magnetic Resonance Imaging, V4, P25, DOI 10.1016/0730-725X(86)91086-6
  • [9] EBERS GC, 1985, ARCH NEUROL-CHICAGO, V42, P702, DOI 10.1001/archneur.1985.04060070096025
  • [10] CRITERIA FOR AN INCREASED SPECIFICITY OF MRI INTERPRETATION IN ELDERLY SUBJECTS WITH SUSPECTED MULTIPLE-SCLEROSIS
    FAZEKAS, F
    OFFENBACHER, H
    FUCHS, S
    SCHMIDT, R
    NIEDERKORN, K
    HORNER, S
    LECHNER, H
    [J]. NEUROLOGY, 1988, 38 (12) : 1822 - 1825