CORTICAL AND SUBCORTICAL GLUCOSE CONSUMPTION MEASURED BY PET IN PATIENTS WITH HUNTINGTONS-DISEASE

被引:216
作者
KUWERT, T
LANGE, HW
LANGEN, KJ
HERZOG, H
AULICH, A
FEINENDEGEN, LE
机构
[1] HEINRICH HEINE UNIV, DEPT PSYCHIAT, DUSSELDORF, GERMANY
[2] HEINRICH HEINE UNIV, DEPT NEUROL, DUSSELDORF, GERMANY
关键词
D O I
10.1093/brain/113.5.1405
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In 23 patients with moderate to severe Huntington's disease (HD) and 21 normal volunteers, the regional cerebral metabolic rate of glucose consumption (rCMRGlc) was measured in the cerebellum, thalamus, striatum, and cortex using positron emission tomography and the 18F-deoxyglucose method. In contrast to previous reports, rCMRGlc was reduced not only in the striatum, but also in the cerebral cortex of patients with HD as compared with normal subjects. No significant difference between HD patients and normal subjects was found for thalamic and cerebellar rCMRGlc. To investigate the relationship between the clinical status and rCMRGlc, correlation coefficients for the clinical data were calculated for absolute values of rCMRGlc and for cerebellar ratios (CR) of rCMRGlc. The duration of chorea correlated significantly only with the absolute values of frontoparietal and temporo-occipital rCMRGlc and with the CRs of most cortical regions evaluated. The severity of chorea correlated significantly only with lentiform nucleus rCMRGlc. The severity of dementia correlated significantly only with the frontoparietal and temporo-occipital rCMRGlc, the CRs of most cortical regions, and the CR for the caudate nucleus. The degree of disability correlated significantly with the CRs of all regions evaluated except the occipital and the superior frontal cortex. It appears from this study that there is a reduction not only for the striatum but also for cortical rCMRGlc in patients with manifest HD, and that the cortical reduction of rCMRGlc contributes to the severity of clinical symptoms in these patients. This challenges the concept that dementia in HD is of purely subcortical origin. © 1990 Oxford University Press.
引用
收藏
页码:1405 / 1423
页数:19
相关论文
共 78 条
[21]   THE DIAGNOSIS OF HUNTINGTONS-DISEASE [J].
FOLSTEIN, SE ;
LEIGH, RJ ;
PARHAD, IM ;
FOLSTEIN, MF .
NEUROLOGY, 1986, 36 (10) :1279-1283
[22]   ALZHEIMERS-DISEASE - FOCAL CORTICAL CHANGES SHOWN BY POSITRON EMISSION TOMOGRAPHY [J].
FOSTER, NL ;
CHASE, TN ;
FEDIO, P ;
PATRONAS, NJ ;
BROOKS, RA ;
DICHIRO, G .
NEUROLOGY, 1983, 33 (08) :961-965
[23]   REGIONAL CEREBRAL OXYGEN-SUPPLY AND UTILIZATION IN DEMENTIA - A CLINICAL AND PHYSIOLOGICAL STUDY WITH O-15 AND POSITRON TOMOGRAPHY [J].
FRACKOWIAK, RSJ ;
POZZILLI, C ;
LEGG, NJ ;
DUBOULAY, GH ;
MARSHALL, J ;
LENZI, GL ;
JONES, T .
BRAIN, 1981, 104 (DEC) :753-778
[24]   REDUCED STRIATAL GLUCOSE CONSUMPTION AND PROLONGED REACTION-TIME ARE EARLY FEATURES IN HUNTINGTONS-DISEASE [J].
GARNETT, ES ;
FIRNAU, G ;
NAHMIAS, C ;
CARBOTTE, R ;
BARTOLUCCI, G .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1984, 65 (02) :231-237
[25]   POSITRON TOMOGRAPHY DEMONSTRATES FRONTAL-LOBE HYPOMETABOLISM IN PROGRESSIVE SUPRANUCLEAR PALSY [J].
GOFFINET, AM ;
DEVOLDER, AG ;
GILLAIN, C ;
RECTEM, D ;
BOL, A ;
MICHEL, C ;
COGNEAU, M ;
LABAR, D ;
LATERRE, C .
ANNALS OF NEUROLOGY, 1989, 25 (02) :131-139
[26]  
HAMACHER K, 1986, J NUCL MED, V27, P235
[27]   GLOBAL CEREBRAL GLUCOSE-UTILIZATION IS INDEPENDENT OF BRAIN SIZE - A PET STUDY [J].
HATAZAWA, J ;
BROOKS, RA ;
DICHIRO, G ;
CAMPBELL, G .
JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY, 1987, 11 (04) :571-576
[28]   GLUCOSE-UTILIZATION RATE VERSUS BRAIN SIZE IN HUMANS [J].
HATAZAWA, J ;
BROOKS, RA ;
DICHIRO, G ;
BACHARACH, SL .
NEUROLOGY, 1987, 37 (04) :583-588
[29]   THE COMBINED USE OF POSITRON EMISSION TOMOGRAPHY AND DNA POLYMORPHISMS FOR PRECLINICAL DETECTION OF HUNTINGTONS-DISEASE [J].
HAYDEN, MR ;
HEWITT, J ;
STOESSL, AJ ;
CLARK, C ;
AMMANN, W ;
MARTIN, WRW .
NEUROLOGY, 1987, 37 (09) :1441-1447
[30]   POSITRON EMISSION TOMOGRAPHY IN THE EARLY DIAGNOSIS OF HUNTINGTONS-DISEASE [J].
HAYDEN, MR ;
MARTIN, WRW ;
STOESSL, AJ ;
CLARK, C ;
HOLLENBERG, S ;
ADAM, MJ ;
AMMANN, W ;
HARROP, R ;
ROGERS, J ;
RUTH, T ;
SAYRE, C ;
PATE, BD .
NEUROLOGY, 1986, 36 (07) :888-894