BENIGN AND SECONDARY PROGRESSIVE MULTIPLE-SCLEROSIS - A PRELIMINARY QUANTITATIVE MRI STUDY

被引:49
作者
FILIPPI, M
BARKER, GJ
HORSFIELD, MA
SACARES, PR
MACMANUS, DG
THOMPSON, AJ
TOFTS, PS
MCDONALD, WI
MILLER, DH
机构
[1] UCL INST NEUROL, NMR RES GRP, LONDON WC1N 3BG, ENGLAND
[2] UCL INST NEUROL, COMP & STAT UNIT, LONDON WC1N 3BG, ENGLAND
关键词
QUANTITATIVE MRI DISABILITY; MULTIPLE SCLEROSIS;
D O I
10.1007/BF00863776
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In a preliminary study, we compared by means of quantitative magnetic resonance imaging (MRI) methods (1) the T2 values and the decay characteristics of chronic brain lesions, (2) the T2 values of normal-appearing frontal white matter (NAWM) and (3) brain lesion volumes in patients with benign and secondary progressive multiple sclerosis (MS) in order to evaluate the mechanisms underlying the development of disability. Eleven clinically definite MS patients with either benign MS (n=5) or secondary progressive MS (n=6) were studied. Fifty-two chronic lesions (identified by comparison with MRI scans obtained at least 12 months previously) were identified. The mean T2 of large lesions (cross-sectional area greater than 41 mm(2)) and of the NAWM was similar in both clinical groups. However, small lesions had higher mean T2 values (P<0.01) in the benign group, probably at least in part because of partial volume effects. Analysis of large lesions revealed biexponential T2 relaxation in 6 of 8 ''secondary progressive'' and in 2 of 16 ''benign'' lesions, perhaps indicating a greater degree of axonal loss in large lesions of patients with secondary progressive MS. Patients with secondary progressive MS had higher (although not significant) total and infratentorial lesion loads than those of the benign group. These preliminary findings suggest, but do not establish, that variations in the extent, site and pathological nature of lesions may all contribute to different patterns of disease evolution in MS.
引用
收藏
页码:246 / 251
页数:6
相关论文
共 29 条
  • [1] PATHOLOGY OF MULTIPLE-SCLEROSIS - PROGRESSION OF LESION
    ADAMS, CWM
    [J]. BRITISH MEDICAL BULLETIN, 1977, 33 (01) : 15 - +
  • [2] HISTOLOGICAL, HISTOCHEMICAL AND BIOCHEMICAL-STUDY OF THE MACROSCOPICALLY NORMAL WHITE MATTER IN MULTIPLE-SCLEROSIS
    ALLEN, IV
    MCKEOWN, SR
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1979, 41 (01) : 81 - 91
  • [3] SEMIAUTOMATED QUALITY ASSURANCE FOR QUANTITATIVE MAGNETIC-RESONANCE-IMAGING
    BARKER, GJ
    TOFTS, PS
    [J]. MAGNETIC RESONANCE IMAGING, 1992, 10 (04) : 585 - 595
  • [4] MAGNETIC-RESONANCE-IMAGING OF EXPERIMENTAL CEREBRAL EDEMA
    BARNES, D
    MCDONALD, WI
    TOFTS, PS
    JOHNSON, G
    LANDON, DN
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1986, 49 (12) : 1341 - 1347
  • [5] QUANTITATIVE NUCLEAR-MAGNETIC-RESONANCE IMAGING - CHARACTERIZATION OF EXPERIMENTAL CEREBRAL EDEMA
    BARNES, D
    MCDONALD, WI
    JOHNSON, G
    TOFTS, PS
    LANDON, DN
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1987, 50 (02) : 125 - 133
  • [6] THE LONGSTANDING MS LESION - A QUANTITATIVE MRI AND ELECTRON-MICROSCOPIC STUDY
    BARNES, D
    MUNRO, PMG
    YOUL, BD
    PRINEAS, JW
    MCDONALD, WI
    [J]. BRAIN, 1991, 114 : 1271 - 1280
  • [7] THE CHARACTERIZATION OF EXPERIMENTAL GLIOSIS BY QUANTITATIVE NUCLEAR MAGNETIC-RESONANCE IMAGING
    BARNES, D
    MCDONALD, WI
    LANDON, DN
    JOHNSON, G
    [J]. BRAIN, 1988, 111 : 83 - 94
  • [8] CASTRO ME, 1987, 6TH ANN M SOC MAGN R, P715
  • [9] FILIPPI M, 1993, NEUROLOGY
  • [10] GOUNOT D, 1989, 8TH ANN M SOC MAGN R, P726