The Amyloid-beta Pathway in Alzheimer's Diseaseopen access
- Authors
- Hampel, Harald; Hardy, John; Blennow, Kaj; Chen, Christopher; Perry, George; Kim, Seung Hyun; Villemagne, Victor L.; Aisen, Paul; Vendruscolo, Michele; Iwatsubo, Takeshi; Masters, Colin L.; Cho, Min; Lannfelt, Lars; Cummings, Jeffrey L.; Vergallo, Andrea
- Issue Date
- Oct-2021
- Publisher
- SPRINGERNATURE
- Citation
- MOLECULAR PSYCHIATRY, v.26, no.10, pp.5481 - 5503
- Indexed
- SCIE
SCOPUS
- Journal Title
- MOLECULAR PSYCHIATRY
- Volume
- 26
- Number
- 10
- Start Page
- 5481
- End Page
- 5503
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/140894
- DOI
- 10.1038/s41380-021-01249-0
- ISSN
- 1359-4184
- Abstract
- Breakthroughs in molecular medicine have positioned the amyloid-beta (A beta) pathway at the center of Alzheimer's disease (AD) pathophysiology. While the detailed molecular mechanisms of the pathway and the spatial-temporal dynamics leading to synaptic failure, neurodegeneration, and clinical onset are still under intense investigation, the established biochemical alterations of the A beta cycle remain the core biological hallmark of AD and are promising targets for the development of disease-modifying therapies. Here, we systematically review and update the vast state-of-the-art literature of A beta science with evidence from basic research studies to human genetic and multi-modal biomarker investigations, which supports a crucial role of A beta pathway dyshomeostasis in AD pathophysiological dynamics. We discuss the evidence highlighting a differentiated interaction of distinct A beta species with other AD-related biological mechanisms, such as tau-mediated, neuroimmune and inflammatory changes, as well as a neurochemical imbalance. Through the lens of the latest development of multimodal in vivo biomarkers of AD, this cross-disciplinary review examines the compelling hypothesis- and data-driven rationale for A beta-targeting therapeutic strategies in development for the early treatment of AD.
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