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The Amyloid-ß Pathway in Alzheimer's Disease.
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.
Afiliação
  • Hampel H; Eisai Inc., Neurology Business Group, Woodcliff Lake, NJ, USA. Harald_Hampel@eisai.com.
  • Hardy J; UK Dementia Research Institute at UCL and Department of Neurodegenerative Disease, UCL Institute of Neurology, University College London, London, UK.
  • Blennow K; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.
  • Chen C; Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
  • Perry G; Memory Aging and Cognition Centre, Departments of Pharmacology and Psychological Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Kim SH; Department of Biology and Neurosciences Institute, University of Texas at San Antonio (UTSA), San Antonio, TX, USA.
  • Villemagne VL; Department of Neurology, College of Medicine, Hanyang University, Seoul, Republic of Korea; Cell Therapy Center, Hanyang University Hospital, Seoul, Republic of Korea.
  • Aisen P; Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.
  • Vendruscolo M; Department of Medicine, The University of Melbourne, Melbourne, VIC, Australia.
  • Iwatsubo T; USC Alzheimer's Therapeutic Research Institute, San Diego, CA, USA.
  • Masters CL; Centre for Misfolding Diseases, Department of Chemistry, University of Cambridge, Cambridge, UK.
  • Cho M; Department of Neuropathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Lannfelt L; Laureate Professor of Dementia Research, Florey Institute and The University of Melbourne, Parkville, VIC, Australia.
  • Cummings JL; Eisai Inc., Neurology Business Group, Woodcliff Lake, NJ, USA.
  • Vergallo A; Uppsala University, Department of of Public Health/Geriatrics, Uppsala, Sweden.
Mol Psychiatry ; 26(10): 5481-5503, 2021 10.
Article em En | MEDLINE | ID: mdl-34456336
Breakthroughs in molecular medicine have positioned the amyloid-ß (Aß) 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 Aß 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 Aß science with evidence from basic research studies to human genetic and multi-modal biomarker investigations, which supports a crucial role of Aß pathway dyshomeostasis in AD pathophysiological dynamics. We discuss the evidence highlighting a differentiated interaction of distinct Aß 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 Aß-targeting therapeutic strategies in development for the early treatment of AD.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Alzheimer Tipo de estudo: Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Alzheimer Tipo de estudo: Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article