Imaging treatment effects in Alzheimer's disease

被引:30
作者
Venneri, Annalena [1 ]
机构
[1] Univ Hull, Clin Neurosci Ctr, Kingston Upon Hull HU6 7RX, N Humberside, England
[2] Univ Modena, Div Neurol, Dept Neurosci, I-41010 Modena, Italy
关键词
MRI; fMRI; SPECT; PET; imaging; Alzheimer's disease; dementia; treatment; ChEI;
D O I
10.1016/j.mri.2007.02.004
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Alzheimer's disease (AD) is the commonest form of degenerative dementia and is characterised by progressive cognitive decline. Despite extensive research, the cause of AD is unknown and there is no cure at present. Of the deficits found in AD, that affecting the cholinergic neurotransmitter system is the best established and the only one translated into symptomatic treatment. Cholinergic enhancement with cholinesterase inhibitor (ChEI) drugs has been achieved and their efficacy and safety ascertained by conventional clinical trials. The mechanism of action of these drugs, however, is not well understood. Imaging with SPECT, PET, MRI and fMRI after treatment has clarified what happens in the brains of those AD patients treated with ChEI drugs. Studies with these techniques have identified increases in brain blood flow and glucose metabolism, restoration of nicotinic receptor function and re-establishment of task-related regional brain activation in response to cognitive stimulation after treatment. Structural MRI studies have explained, to some degree, why only a proportion of patients benefits from ChEI treatment and there is some evidence that some ChEI drugs might be neuroprotective. There are, however, many unsolved problems. Timing of treatment intervention to obtain maximum response and the determinants of treatment response are mostly unknown. It is also unclear whether administration of treatment in those patients who have no potential for response accelerates disease progression. These issues cannot be solved by conventional clinical trials. Pharmacoimaging studies could assist the development and refinement of drugs to treat those diseases, such as AD, which affect the central nervous system. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:953 / 968
页数:16
相关论文
共 92 条
[1]  
Alzheimer A., 1907, ALLG Z PSYCHIAT, V64, P146, DOI DOI 10.1002/CA.980080612
[2]  
[Anonymous], COCHRANE DATABASE SY
[3]  
[Anonymous], COCHRANE DATABASE SY
[4]   Effects of cholinergic enhancement on visual stimulation, spatial attention, and spatial working memory [J].
Bentley, P ;
Husain, M ;
Dolan, RJ .
NEURON, 2004, 41 (06) :969-982
[5]   Cholinergic enhancement modulates neural correlates of selective attention and emotional processing [J].
Bentley, P ;
Vuilleumier, P ;
Thiel, CM ;
Driver, J ;
Dolan, RJ .
NEUROIMAGE, 2003, 20 (01) :58-70
[6]   Effects of attention and emotion on repetition priming and their modulation by cholinergic enhancement [J].
Bentley, P ;
Vuilleumier, P ;
Thiel, CM ;
Driver, J ;
Dolan, RJ .
JOURNAL OF NEUROPHYSIOLOGY, 2003, 90 (02) :1171-1181
[7]   Galantamine provides sustained benefits in patients with 'advanced moderate' Alzheimer's disease for at least 12 months [J].
Blesa, R ;
Davidson, M ;
Kurz, A ;
Reichman, W ;
van Baelen, B ;
Schwalen, S .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2003, 15 (02) :79-87
[8]   Cholinergic neurotransmission has different effects on cerebral glucose consumption and blood flow in young normals, aged normals, and Alzheimer's disease patients [J].
Blin, J ;
Ivanoiu, A ;
Coppens, A ;
De Volder, A ;
Labar, D ;
Michel, C ;
Laterre, EC .
NEUROIMAGE, 1997, 6 (04) :335-343
[9]   Degree of inhibition of cortical acetylcholinesterase activity and cognitive effects by donepezil treatment in Alzheimer's disease [J].
Bohnen, NI ;
Kaufer, DI ;
Hendrickson, R ;
Ivanco, LS ;
Lopresti, BJ ;
Koeppe, RA ;
Meltzer, CC ;
Constantine, G ;
Davis, JG ;
Mathis, CA ;
DeKosky, ST ;
Moore, RY .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2005, 76 (03) :315-319
[10]   NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259