Axonal dysfunction and disability in a relapse of multiple sclerosis: Longitudinal study of a patient

被引:61
作者
DeStefano, N
Matthews, PM
Narayanan, S
Francis, GS
Antel, JP
Arnold, DL
机构
[1] MONTREAL NEUROL HOSP & INST,DEPT NEUROL & NEUROSURG,MONTREAL,PQ H3A 2B4,CANADA
[2] UNIV SIENA,INST NEUROL SCI,NEUROMETAB UNIT,I-53100 SIENA,ITALY
[3] UNIV OXFORD,RADCLIFFE INFIRM,DEPT CLIN NEUROL,OXFORD OX2 6HE,ENGLAND
关键词
D O I
10.1212/WNL.49.4.1138
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In a 6-year longitudinal study of a patient with relapsing progressive multiple sclerosis (MS), we used proton magnetic resonance spectroscopy to assess N-acetylaspartate (NAA) from a large central brain volume to evaluate the relationship between this marker of neuronal integrity and clinical disability. During the follow-up period, there was one major relapse and its subsequent partial remission. Changes in the brain NAA to creatine ratio correlated strongly with clinical disability (Spearman rank coefficient = -0.73, p < 0.001). We interpret this as evidence that axonal dysfunction or loss contributes to functional impairment of patients with MS. Because the NAA signal in the large volume of interest originated predominantly from white matter that appeared normal on conventional MRI, these results also suggest that some degree of axonal dysfunction may be widespread in acute, severe relapses.
引用
收藏
页码:1138 / 1141
页数:4
相关论文
共 12 条
[1]   USE OF PROTON MAGNETIC-RESONANCE SPECTROSCOPY FOR MONITORING DISEASE PROGRESSION IN MULTIPLE-SCLEROSIS [J].
ARNOLD, DL ;
RIESS, GT ;
MATTHEWS, PM ;
FRANCIS, GS ;
COLLINS, DL ;
WOLFSON, C ;
ANTEL, JP .
ANNALS OF NEUROLOGY, 1994, 36 (01) :76-82
[2]   THE PROTON NMR-SPECTRUM IN ACUTE EAE - THE SIGNIFICANCE OF THE CHANGE IN THE CHO-CR RATIO [J].
BRENNER, RE ;
MUNRO, PMG ;
WILLIAMS, SCR ;
BELL, JD ;
BARKER, GJ ;
HAWKINS, CP ;
LANDON, DN ;
MCDONALD, WI .
MAGNETIC RESONANCE IN MEDICINE, 1993, 29 (06) :737-745
[3]   Persistent functional deficit in multiple sclerosis and autosomal dominant cerebellar ataxia is associated with axon loss [J].
Davie, CA ;
Barker, GJ ;
Webb, S ;
Tofts, PS ;
Thompson, AJ ;
Harding, AE ;
McDonald, WI ;
Miller, DH .
BRAIN, 1995, 118 :1583-1592
[4]   Chemical pathology of acute demyelinating lesions and its correlation with disability [J].
DeStefano, N ;
Matthews, PM ;
Antel, JP ;
Preul, M ;
Francis, G ;
Arnold, DL .
ANNALS OF NEUROLOGY, 1995, 38 (06) :901-909
[5]   A spinal cord MRI study of benign and secondary progressive multiple sclerosis [J].
Filippi, M ;
Campi, A ;
Colombo, B ;
Pereira, C ;
Martinelli, V ;
Baratti, C ;
Comi, G .
JOURNAL OF NEUROLOGY, 1996, 243 (07) :502-505
[6]   BIOCHEMICAL-ALTERATIONS IN MULTIPLE-SCLEROSIS LESIONS AND NORMAL-APPEARING WHITE-MATTER DETECTED BY IN-VIVO P-31 AND H-1 SPECTROSCOPIC IMAGING [J].
HUSTED, CA ;
GOODIN, DS ;
HUGG, JW ;
MAUDSLEY, AA ;
TSURUDA, JS ;
DEBIE, SH ;
FEIN, G ;
MATSON, GB ;
WEINER, MW .
ANNALS OF NEUROLOGY, 1994, 36 (02) :157-165
[7]   Cerebrospinal fluid from multiple sclerosis patients inactivates neuronal Na+ current [J].
Koller, H ;
Buchholz, J ;
Siebler, M .
BRAIN, 1996, 119 :457-463
[8]   Guidelines for the use of magnetic resonance techniques in monitoring the treatment of multiple sclerosis [J].
Miller, DH ;
Albert, PS ;
Barkhof, F ;
Francis, G ;
Frank, JA ;
Hodgkinson, S ;
Lublin, FD ;
Paty, DW ;
Reingold, SC ;
Simon, J .
ANNALS OF NEUROLOGY, 1996, 39 (01) :6-16
[9]   Transient increase in symptoms associated with cytokine release in patients with multiple sclerosis [J].
Moreau, T ;
Coles, A ;
Wing, M ;
Isaacs, J ;
Hale, G ;
Waldmann, H ;
Compston, A .
BRAIN, 1996, 119 :225-237
[10]   Evaluation of multiple sclerosis by H-1 spectroscopic imaging at 4.1 T [J].
Pan, JW ;
Hetherington, HP ;
Vaughan, JT ;
Mitchell, G ;
Pohost, GM ;
Whitaker, JN .
MAGNETIC RESONANCE IN MEDICINE, 1996, 36 (01) :72-77