期刊
ALZHEIMERS & DEMENTIA
卷 9, 期 4, 页码 459-462出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.jalz.2012.07.002
关键词
Biomarkers; Alzheimer's disease; Brain amyloidosis; Toxicity; Amyloid; Tau; Longitudinal studies
资金
- Swedish Research Council
Certain preparations of Alzheimer-associated amyloid beta (A beta) exhibit rapid (within minutes) synaptotoxicity when applied to hippocampal slices or neuronal cell cultures, or when injected into the central nervous system of rodents. In addition, it is well known that some elderly people have brain amyloidosis without showing signs of cognitive impairment or neurodegeneration beyond the age norm. Biomarkers, reviewed extensively in a recent Perspectives article in Alzheimer's & Dementia, suggest that amyloid-positive individuals are at higher risk of Alzheimer's disease than similarly aged individuals without evidence of brain amyloidosis, provided they live long enough. But how can the brain resist amyloid pathology for many years? Here, we expand on recent biomarker studies suggesting that A beta build-up and toxicity may occur in two phases. We hypothesize that the first phase may involve an autocatalytic build-up of a nontoxic A beta reservoir, tentatively named the A beta(Cat) pool, and that gain of toxicity may require brain incubation of A beta in the water-deprived plaque milieu over years to produce modified forms of the protein that are truly neurotoxic (A beta(Tox)). We argue for the need to describe the molecular natures of A beta(Cat) and A beta(Tox) in greater detail as a means to gain success in anti-A beta disease-modifying drug development. (C) 2013 The Alzheimer's Association. All rights reserved.
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