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Cited 37 time in webofscience Cited 42 time in scopus
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The Amyloid-beta Pathway in Alzheimer's Diseaseopen access

Authors
Hampel, HaraldHardy, JohnBlennow, KajChen, ChristopherPerry, GeorgeKim, Seung HyunVillemagne, Victor L.Aisen, PaulVendruscolo, MicheleIwatsubo, TakeshiMasters, Colin L.Cho, MinLannfelt, LarsCummings, 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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