Is Alzheimer's disease a neurodegenerative or a vascular disorder? Data, dogma, and dialectics

被引:693
作者
de la Torre, JC [1 ]
机构
[1] Case Western Reserve Univ, Inst Pathol, Cleveland, OH 44106 USA
关键词
D O I
10.1016/S1474-4422(04)00683-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The cause of Alzheimer's disease (AD) is unknown. This gap in knowledge has created a stumbling block in the search for a genuinely effective treatment or cure for this dementia. This article summarises the arguments for a causal role for either amyloid deposition or cerebrovascular pathology as the primary trigger in the development of non-genetic AD. A bare-bones survey of the published research reveals no compelling evidence that amyloid deposition is neurotoxic in human beings or that it results in neurodegenerative changes involving synaptic, metabolic, or neuronal loss in human or transgenic-mouse brains. By contrast, the data supporting AD as a primary vascular disorder are more convincing. Findings suggesting a vascular cause of AD come from epidemiological, neuroimaging, pathological, pharmacotherapeutic, and clinical studies. The consensus of these studies indicates that chronic brain hypoperfusion is linked to AD risk factors, AD preclinical detection and pharmacotherapeutic action of AD symptoms.
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页码:184 / 190
页数:7
相关论文
共 104 条
[1]   Atherosclerotic lesions and mitochondria DNA deletions in brain microvessels as a central target for the development of human AD and AD-Like pathology in aged transgenic mice [J].
Aliev, G ;
Seyidova, D ;
Neal, ML ;
Shi, J ;
Lamb, BT ;
Siedlak, SL ;
Vinters, HV ;
Head, E ;
Perry, G ;
Lamanna, JC ;
Friedland, RP ;
Cotman, CW .
ALZHEIMER'S DISEASE: VASCULAR ETIOLOGY AND PATHOLOGY, 2002, 977 :45-64
[2]   Mitochondria and vascular lesions as a central target for the development of Alzheimer's disease and Alzheimer disease-like pathology in transgenic mice [J].
Aliev, G ;
Seyidova, D ;
Lamb, BT ;
Obrenovich, ME ;
Siedlak, SL ;
Vinters, HV ;
Friedland, RP ;
LaManna, JC ;
Smith, MA ;
Perry, G .
NEUROLOGICAL RESEARCH, 2003, 25 (06) :665-674
[3]  
ALTER M, 1986, Neuroepidemiology, V5, P148, DOI 10.1159/000110824
[4]  
*AM PSYCH ASS, 1994, DIAGN STAT MAN MENT, P138
[5]   WOMEN, MYOCARDIAL-INFARCTION, AND DEMENTIA IN THE VERY OLD [J].
ARONSON, MK ;
OOI, WL ;
MORGENSTERN, H ;
HAFNER, A ;
MASUR, D ;
CRYSTAL, H ;
FRISHMAN, WH ;
FISHER, D ;
KATZMAN, R .
NEUROLOGY, 1990, 40 (07) :1102-1106
[6]   NEUROFIBRILLARY TANGLES BUT NOT SENILE PLAQUES PARALLEL DURATION AND SEVERITY OF ALZHEIMERS-DISEASE [J].
ARRIAGADA, PV ;
GROWDON, JH ;
HEDLEYWHYTE, ET ;
HYMAN, BT .
NEUROLOGY, 1992, 42 (03) :631-639
[7]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[8]   Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization [J].
Asahara, T ;
Masuda, H ;
Takahashi, T ;
Kalka, C ;
Pastore, C ;
Silver, M ;
Kearne, M ;
Magner, M ;
Isner, JM .
CIRCULATION RESEARCH, 1999, 85 (03) :221-228
[9]   Short-term β-amyloid vaccinations do not improve cognitive performance in cognitively impaired APP+PS1 mice [J].
Austin, L ;
Arendash, GW ;
Gordon, MN ;
Diamond, DM ;
DiCarlo, G ;
Dickey, C ;
Ugen, K ;
Morgan, D .
BEHAVIORAL NEUROSCIENCE, 2003, 117 (03) :478-484
[10]   Cognitive disorders in patients with occlusive disease of the carotid artery: a systematic review of the literature [J].
Bakker, FC ;
Klijn, CJM ;
Jennekens-Schinkel, A ;
Kappelle, LJ .
JOURNAL OF NEUROLOGY, 2000, 247 (09) :669-676