A magnetization transfer histogram study of normal-appearing brain tissue in MS

被引:151
作者
Tortorella, C
Viti, B
Bozzali, M
Sormani, MP
Rizzo, G
Gilardi, MF
Comi, G
Filippi, M
机构
[1] Sci Inst Osped San Raffaele, Dept Neurosci, Neuroimaging Res Unit, I-20132 Milan, Italy
[2] Sci Inst Osped San Raffaele, Dept Neurosci, Unit Clin Trials, I-20132 Milan, Italy
[3] Sci Inst Osped San Raffaele, Dept Nucl Med, I-20132 Milan, Italy
[4] Inst Canc Res, Unit Clin Epidemiol & Trials, Genoa, Italy
关键词
MS; MRI; magnetization transfer imaging; normal-appearing brain tissue;
D O I
10.1212/WNL.54.1.186
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To evaluate 1) the ability of magnetization transfer ratio (MTR) histogram analysis to detect the extent of changes occurring outside MS lesions seen on conventional scans, 2) whether such changes vary in the different MS clinical phenotypes, 3) whether the changes are associated with the extent and severity of the macroscopic lesion load, and 4) the contribution to brain atrophy. Methods: Dual-echo, T1-weighted, and MT scans of the brain were obtained from 77 patients with varying MS courses and 20 age- and sex-matched control subjects. To create MT histograms of the normal-appearing cerebral tissue, MS lesions were segmented from dual-echo scans, superimposed automatically, and nulled out from the coregistered and scalp-stripped MTR maps. Average MTR, peak height, and peak position were considered. T2 and T1 lesion loads, average lesion MTR, and brain volume were also measured. Results: Average histogram MTR. (p < 0.0001) and peak position (p ( 0.0001) from patients with relapsing-remitting MS (RMMS) were lower than those from control subjects. Patients with primary progressive MS (PPMS) had lower average histogram MTR (p = 0.002) and histogram peak height (p = 0.01) than control subjects. Patients with secondary progressive MS (SPMS) had a lower peak height (p = 0.05) than those with RRMS. Average lesion MTR (p < 0.0001) correlated highly with the histogram MTR. Average histogram MTR (p < 0.0001) and T2 lesion load (p = 0.001) correlated highly with brain volume. Conclusions: The amount of microscopic changes account for an important fraction of the lesion load in MS. They may contribute to the development of brain atrophy and tend to be more evident in patients with secondary progressive MS.
引用
收藏
页码:186 / 193
页数:8
相关论文
共 60 条
[1]   PATHOLOGY OF MULTIPLE-SCLEROSIS - PROGRESSION OF LESION [J].
ADAMS, CWM .
BRITISH MEDICAL BULLETIN, 1977, 33 (01) :15-+
[2]   HISTOLOGICAL, HISTOCHEMICAL AND BIOCHEMICAL-STUDY OF THE MACROSCOPICALLY NORMAL WHITE MATTER IN MULTIPLE-SCLEROSIS [J].
ALLEN, IV ;
MCKEOWN, SR .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1979, 41 (01) :81-91
[3]   STUDIES ON PATHOGENESIS OF MULTIPLE-SCLEROSIS - PARTICIPATION OF LYSOSOMES ON DEMYELINATION IN CENTRAL NERVOUS-SYSTEM WHITE MATTER OUTSIDE PLAQUES [J].
ARSTILA, AU ;
RIEKKINEN, P ;
RINNE, UK ;
LAITINEN, L .
EUROPEAN NEUROLOGY, 1973, 9 (01) :1-20
[4]   MAGNETIC-RESONANCE RELAXATION-TIME MAPPING IN MULTIPLE-SCLEROSIS - NORMAL APPEARING WHITE-MATTER AND THE INVISIBLE LESION LOAD [J].
BARBOSA, S ;
BLUMHARDT, LD ;
ROBERTS, N ;
LOCK, T ;
EDWARDS, RHT .
MAGNETIC RESONANCE IMAGING, 1994, 12 (01) :33-42
[5]   Inflammatory central nervous system demyelination: Correlation of magnetic resonance imaging findings with lesion pathology [J].
Bruck, W ;
Bitsch, A ;
Kolenda, H ;
Bruck, Y ;
Stiefel, M ;
Lassmann, H .
ANNALS OF NEUROLOGY, 1997, 42 (05) :783-793
[6]  
COMPSTON A, 1998, SYMPTOMS SIGNS MULTI
[7]   1H magnetic resonance spectroscopy of chronic cerebral white matter lesions and normal appearing white matter in multiple sclerosis [J].
Davie, CA ;
Barker, GJ ;
Thompson, AJ ;
Tofts, PS ;
McDonald, WI ;
Miller, DH .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1997, 63 (06) :736-742
[8]   In vivo evidence for axonal dysfunction remote from focal cerebral demyelination of the type seen in multiple sclerosis [J].
De Stefano, N ;
Narayanan, S ;
Matthews, PM ;
Francis, GS ;
Antel, JP ;
Arnold, DL .
BRAIN, 1999, 122 :1933-1939
[9]   Axonal dysfunction and disability in a relapse of multiple sclerosis: Longitudinal study of a patient [J].
DeStefano, N ;
Matthews, PM ;
Narayanan, S ;
Francis, GS ;
Antel, JP ;
Arnold, DL .
NEUROLOGY, 1997, 49 (04) :1138-1141
[10]   EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS AND MULTIPLE-SCLEROSIS - LESION CHARACTERIZATION WITH MAGNETIZATION TRANSFER IMAGING [J].
DOUSSET, V ;
GROSSMAN, RI ;
RAMER, KN ;
SCHNALL, MD ;
YOUNG, LH ;
GONZALEZSCARANO, F ;
LAVI, E ;
COHEN, JA .
RADIOLOGY, 1992, 182 (02) :483-491