期刊
CURRENT PHARMACEUTICAL DESIGN
卷 17, 期 25, 页码 2594-2602出版社
BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/138161211797416039
关键词
Alzheimer's disease; Amyloid; APP; biomarker; theragnostic marker
资金
- Swedish Research Council [2006-6227, 2006-2740, 2006-3505]
- Alzheimer's Association [NIRG-08-90356]
- cNEUPRO
- Royal Swedish Academy of Sciences
- Sahlgrenska University Hospital
- Inga-Britt and Arne Lundberg Research Foundation
- Goteborg Medical Society
- Swedish Medical Society
- Swedish Brain Power
- Stiftelsen Gamla Tjanarinnor
- Gun och Bertil Stohnes stiftelse
- Ahlen-stiftelsen
- Alzheimer Foundation, Sweden
The last decades have witnessed an explosion in studies of the role of amyloid-beta (A beta) in the progress of the neurodegenerative disorder Alzheimer's disease (AD) and it is now widely accepted that A beta is related to the pathogenesis of AD. For example, studies have shown that A beta is neurotoxic and that the neurotoxicity of A beta is related to its aggregation state. The concentration of the 42 amino acid form of A beta (A beta 1-42) is reduced in the cerebrospinal fluid (CSF) from AD patients, which is believed to reflect the AD pathology with plaques in the brain acting as sinks. Less well investigated, however, is the ability of other A beta isoforms to distinguish AD patients from controls and to identify treatment effects in clinical trials. Recently, novel C-truncated forms of A beta (A beta 1-14, A beta 1-15, and A beta 1-16) were identified in human CSF. The presence of these small peptides is consistent with a catabolic amyloid precursor protein cleavage pathway by beta- followed by alpha-secretase. It has been shown that A beta 1-14, A beta 1-15, and A beta 1-16 increase dose-dependently in response to gamma-secretase inhibitor treatment while A beta 1-42 levels are unchanged. Here, we review the many aspects of A beta and its isoforms with special focus on their potential role as diagnostic and theragnostic markers.
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