Impairment of neocortical metabolism predicts progression in Alzheimer's disease

被引:90
作者
Herholz, K
Nordberg, A
Salmon, E
Perani, D
Kessler, J
Mielke, R
Halber, M
Jelic, V
Almkvist, O
Collette, F
Alberoni, M
Kennedy, A
Hasselbalch, S
Fazio, F
Heiss, WD
机构
[1] Max Planck Inst Neurol Forsch, D-50931 Cologne, Germany
[2] Karolinska Inst, Huddinge Univ Hosp, Dept Clin Neurosci & Family Med, Huddinge, Sweden
[3] Univ Liege, Unite Med Cyclotron, B-4000 Liege, Belgium
[4] Univ Liege, Dept Neurol, B-4000 Liege, Belgium
[5] Ist Neurosci & Bioimmagini, Milan, Italy
[6] Hammersmith Hosp, MRC, Cyclotron Unit, London W12 0HS, England
[7] Rigshosp, Dept Neurol, DK-2100 Copenhagen, Denmark
关键词
Alzheimer's disease; cerebral glucose metabolism; emission computed tomography fluorodeoxyglucose; F-18-labeled; prospective study; multicenter study;
D O I
10.1159/000017196
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Progression rates of Alzheimer's disease (AD) vary considerably, and they are particularly difficult to predict in patients with mild cognitive impairment. We performed a prospective multicenter cohort study in 186 patients with possible or probable AD, mostly with presenile onset. In a cross-sectional analysis at entry, impairment of glucose metabolism in temporoparietal or frontal association areas measured with positron emission tomography was significantly associated with dementia severity, clinical classification as possible versus probable AD, presence of multiple cognitive deficits and history of progression. A prospective longitudinal analysis showed a significant association between initial metabolic impairment and subsequent clinical deterioration. In patients with mild cognitive deficits at entry, the risk of deterioration was up to 4.7 times higher if the metabolism was severely impaired than with mild or absent metabolic impairment. Copyright (C) 1999 S. Karger AG. Basel.
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页码:494 / 504
页数:11
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