A longitudinal study of cerebral glucose metabolism, MRI, and disability in patients with MS

被引:48
作者
Blinkenberg, M
Jensen, CV
Holm, S
Paulson, OB
Sorensen, PS
机构
[1] Univ Copenhagen Hosp, Rigshosp, MS Res Unit, DK-2100 Copenhagen, Denmark
[2] Univ Copenhagen Hosp, Rigshosp, Neurobiol Res Unit, Dept Neurol, DK-2100 Copenhagen, Denmark
[3] Univ Copenhagen Hosp, Rigshosp, Dept Nucl Med, DK-2100 Copenhagen, Denmark
[4] Univ Copenhagen, Hvidovre Hosp, Danish Res ctr Magnet Resonance, DK-2650 Hvidovre, Denmark
关键词
D O I
10.1212/WNL.53.1.149
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To study the time-related changes in cerebral metabolic rate of glucose (CMRglc) in MS patients and to correlate these with changes in MRI lesion load and disability. Background: Measurements of MRI lesion load and neurologic disability are used widely to monitor disease progression in longitudinal studies of MS patients, but little is known about the associated changes in cerebral neural function. Methods: The authors studied 10 patients with clinically definite MS who underwent serial measurements of CMRglc, MRI T2-weighted total lesion area (TLA), and clinical evaluation of disability (Expanded Disability Status Scale [EDSS]) over a period of approximately 2 years (three examinations). CMRglc was calculated using PET and 18-fluorodeoxyglucose (FDG). Results: The global cortical CMRglc decreased with time (p < 0.001) and the most pronounced reductions of CMRglc were detected in frontal and parietal cortical areas. There was a statistically significant increase of disability (p < 0.01) and TLA (p < 0.05) measurements during the study, but changes in CMRglc were not correlated to changes in TLA and EDSS. Conclusions: Global cortical cerebral metabolism in MS is decreased significantly during a 2-year observation period, suggesting a deterioration of cortical activity with disease progression. The time-related changes of cortical CMRglc are statistically stronger than changes in TLA measurements and neurologic disability, and might be a useful secondary measure of treatment efficacy.
引用
收藏
页码:149 / 153
页数:5
相关论文
共 35 条
[11]  
KURTZKE JF, 1983, NEUROLOGY, V33, P1444, DOI 10.1212/WNL.33.11.1444
[12]  
LOESSNER A, 1995, J NUCL MED, V36, P1141
[13]   Progressive cerebral atrophy in multiple sclerosis - A serial MRI study [J].
Losseff, NA ;
Wang, L ;
Lai, HM ;
Yoo, DS ;
GawneCain, ML ;
McDonald, WI ;
Miller, DH ;
Thompson, AJ .
BRAIN, 1996, 119 :2009-2019
[14]   REGIONAL CEREBRAL BLOOD-FLOW IN MULTIPLE-SCLEROSIS MEASURED BY SINGLE PHOTON-EMISSION TOMOGRAPHY WITH TC-99M HEXAMETHYL-PROPYLENEAMINE OXIME [J].
LYCKE, J ;
WIKKELSO, C ;
BERGH, AC ;
JACOBSSON, L ;
ANDERSEN, O .
EUROPEAN NEUROLOGY, 1993, 33 (02) :163-167
[15]   Correlation between brain MRI lesion volume and disability in patients with multiple sclerosis [J].
Mammi, S ;
Filippi, M ;
Martinelli, V ;
Campi, A ;
Colombo, B ;
Scotti, G ;
Canal, N ;
Comi, G .
ACTA NEUROLOGICA SCANDINAVICA, 1996, 94 (02) :93-96
[16]   REPRODUCIBILITY OF CEREBRAL GLUCOSE-UTILIZATION MEASURED BY PET AND THE [F-18] 2-FLUORO-2-DEOXY-D-GLUCOSE METHOD IN RESTING, HEALTHY-HUMAN SUBJECTS [J].
MAQUET, P ;
DIVE, D ;
SALMON, E ;
VONFRENCKEL, R ;
FRANCK, G .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 1990, 16 (4-6) :267-273
[17]   ANALYSIS OF SERIAL MEASUREMENTS IN MEDICAL-RESEARCH [J].
MATTHEWS, JNS ;
ALTMAN, DG ;
CAMPBELL, MJ ;
ROYSTON, P .
BRITISH MEDICAL JOURNAL, 1990, 300 (6719) :230-235
[18]   The metabolic topography of normal aging [J].
Moeller, JR ;
Ishikawa, T ;
Dhawan, V ;
Spetsieris, P ;
Mandel, F ;
Alexander, GE ;
Grady, C ;
Pietrini, P ;
Eidelberg, D .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (03) :385-398
[19]   INTERFERON BETA-1B IS EFFECTIVE IN RELAPSING-REMITTING MULTIPLE-SCLEROSIS .2. MRI ANALYSIS RESULTS OF A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL [J].
PATY, DW ;
LI, DKB ;
DUQUETTE, P ;
GIRARD, M ;
DESPAULT, L ;
DUBOIS, R ;
KNOBLER, RL ;
LUBLIN, FD ;
KELLEY, L ;
FRANCIS, GS ;
LAPIERRE, Y ;
ANTEL, J ;
FREEDMAN, M ;
HUM, S ;
GREENSTEIN, JI ;
MISHRA, B ;
MULDOON, J ;
WHITAKER, JN ;
EVANS, BK ;
LAYTON, B ;
SIBLEY, WA ;
LAGUNA, J ;
KRIKAWA, J ;
PATY, DW ;
OGER, JJ ;
KASTRUKOFF, LF ;
MOORE, GRW ;
HASHIMOTO, SA ;
MORRISON, W ;
NELSON, J ;
GOODIN, DS ;
MASSA, SM ;
GUTTERIDGE, E ;
ARNASON, BGW ;
NORONHA, A ;
REDER, AT ;
MARTIA, R ;
EBERS, GC ;
RICE, GPA ;
LESAUX, J ;
JOHNSON, KP ;
PANITCH, HS ;
BEVER, CT ;
CONWAY, K ;
WALLENBERG, JC ;
BEDELL, L ;
VANDENNOORT, S ;
WEINSHENKER, B ;
WEISS, W ;
REINGOLD, S .
NEUROLOGY, 1993, 43 (04) :662-667
[20]   Functional basis of memory impairment in multiple sclerosis: A [F-18]FDG PET study [J].
Paulesu, E ;
Perani, D ;
Fazio, F ;
Comi, G ;
Pozzilli, C ;
Martinelli, V ;
Filippi, M ;
Bettinardi, V ;
Sirabian, G ;
Passafiume, D ;
Anzini, A ;
Lenzi, GL ;
Canal, N ;
Fieschi, C .
NEUROIMAGE, 1996, 4 (02) :87-96