PATTERNS OF CEREBRAL GLUCOSE-METABOLISM DETECTED WITH POSITION EMISSION TOMOGRAPHY DIFFER IN MULTIPLE SYSTEM ATROPHY AND OLIVOPONTOCEREBELLAR ATROPHY

被引:73
作者
GILMAN, S
KOEPPE, RA
JUNCK, L
KLUIN, KJ
LOHMAN, M
STLAURENT, RT
机构
[1] UNIV MICHIGAN,CTR MED,DEPT INTERNAL MED,ANN ARBOR,MI 48109
[2] UNIV MICHIGAN,CTR MED,DEPT PHYS MED & REHABIL,ANN ARBOR,MI 48109
[3] UNIV MICHIGAN,SCH PUBL HLTH,DEPT BIOSTAT,ANN ARBOR,MI 48109
关键词
D O I
10.1002/ana.410360208
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We used positron emission tomography with [F-18]fluorodeoxyglucose to study local cerebral metabolic rates for glucose (1CMRglc) in patients with multiple system atrophy (MSA), sporadic olivopontocerebellar atrophy (sOPCA), and dominantly inherited olivopontocerebellar atrophy (dOPCA) in comparison with normal control subjects. In MSA, absolute 1CMRglc was significantly decreased in the brainstem, cerebellum, putamen, thalamus, and cerebral cortex. In sOPCA, absolute 1CMRglc was significantly decreased in the brainstem, cerebellum, putamen, thalamus, and cerebral cortex. In sOPCA, absolute 1CMRglc was significantly decreased in the brainstem and cerebellum but not in the other structures. Examination of 1CMRglc normalized to the cerebral cortex in comparison with normal controls revealed in MSA significant decreases in the brainstem, cerebellum, and putamen but, in both sOPCA and dOPCA, significant decreases only in the brainstem and cerebellum. The findings indicate that these three disorders all show a marked decrease of 1CMRglc in the brainstem and cerebellum but differ in the degree of hypometabolism in forebrain and cerebral cortical structures. The results are consistent with the possibility that, in many cases, sOPCA will evolve into MSA. Moreover, positron emission tomography may provide helpful diagnostic information in these neurodegenerative diseases.
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页码:166 / 175
页数:10
相关论文
共 37 条
[1]   DEGENERATIVE DISEASES OF NERVOUS-SYSTEM ASSOCIATED WITH AUTONOMIC FAILURE [J].
BANNISTER, R ;
OPPENHEIMER, DR .
BRAIN, 1972, 95 :457-+
[2]   STRIATONIGRAL DEGENERATIONS - PUTAMINAL PIGMENTS AND NOSOLOGY [J].
BORIT, A ;
RUBINSTEIN, LJ ;
URICH, H .
BRAIN, 1975, 98 (MAR) :101-&
[3]   THE DIAGNOSIS OF MULTIPLE SYSTEM ATROPHY - REPLY [J].
BROOKS, DJ .
ANNALS OF NEUROLOGY, 1991, 29 (06) :690-690
[4]  
CHOKROVERTY S, 1984, OLIVOPONTOCEREBELLAR, P104
[5]   SOMATIC AND AUTONOMIC FUNCTION IN PROGRESSIVE AUTONOMIC FAILURE AND MULTIPLE SYSTEM ATROPHY [J].
COHEN, J ;
LOW, P ;
FEALEY, R ;
SHEPS, S ;
JIANG, NS .
ANNALS OF NEUROLOGY, 1987, 22 (06) :692-699
[6]   DECREASED GLUCOSE-UTILIZATION IN THE STRIATUM AND FRONTAL-LOBE IN PROBABLE STRIATONIGRAL DEGENERATION [J].
DEVOLDER, AG ;
FRANCART, J ;
LATERRE, C ;
DOOMS, G ;
BOL, A ;
MICHEL, C ;
GOFFINET, AM .
ANNALS OF NEUROLOGY, 1989, 26 (02) :239-247
[7]  
EADIE MJ, 1975, HDB CLIN NEUROLOGY 1, V21, P415
[8]   STRIATAL HYPOMETABOLISM DISTINGUISHES STRIATONIGRAL DEGENERATION FROM PARKINSONS-DISEASE [J].
EIDELBERG, D ;
TAKIKAWA, S ;
MOELLER, JR ;
DHAWAN, V ;
REDINGTON, K ;
CHALY, T ;
ROBESON, W ;
DAHL, JR ;
MARGOULEFF, D ;
FAZZINI, E ;
PRZEDBORSKI, S ;
FAHN, S .
ANNALS OF NEUROLOGY, 1993, 33 (05) :518-527
[9]   STRIATONIGRAL DEGENERATION - A CLINICOPATHOLOGICAL STUDY [J].
FEARNLEY, JM ;
LEES, AJ .
BRAIN, 1990, 113 :1823-1842
[10]  
Fulham M J, 1991, Clin Auton Res, V1, P27, DOI 10.1007/BF01826055