| Literature DB >> 24852227 |
Henrik Zetterberg1, Niklas Mattsson.
Abstract
The increasing prevalence of Alzheimer's disease (AD) and a lack of effective prevention or disease-modifying therapies are global challenges with devastating personal, social and economic consequences. The amyloid β (Aβ) hypothesis posits that cerebral β-amyloidosis is a critical early event in AD pathogenesis. However, failed clinical trials of Aβ-centric drug candidates have called this hypothesis into question. Whereas we acknowledge that the Aβ hypothesis is far from disproven, we here re-visit the links between Aβ, tau and neurodegeneration. We review the genetics, epidemiology and pathology of sporadic AD and give an updated account of what is currently known about the molecular pathogenesis of the disease.Entities:
Keywords: Alzheimer’s disease; aging; amyloid; apolipoprotein E; neurodegeneration; pathogenesis; tau
Mesh:
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Year: 2014 PMID: 24852227 DOI: 10.1586/14737175.2014.915740
Source DB: PubMed Journal: Expert Rev Neurother ISSN: 1473-7175 Impact factor: 4.618