| Literature DB >> 31243509 |
Christian Haass1,2,3, Johannes Levin4,5.
Abstract
Numerous amyloid-based clinical studies have recently failed. Does this mean that the mechanisms of Alzheimer's disease have to be reinvestigated and that amyloid is not the trigger of the disease? Strong genetic evidence from familial Alzheimer's disease contradicts this fatalistic opinion. Mutations in all genes associated with familial Alzheimer's disease affect amyloid metabolism and aggregation. Moreover, a protective mutation reduces amyloid production by 20-30% throughout the lifetime. Clinical studies rather failed because secretase inhibitors block cleavage of numerous other physiologically important substrates of secretases. Moreover, the disease is initiated decades before symptoms occur. Successful treatment attempts with anti-amyloid medication based on other prototype amyloidoses are described. Finally, new therapeutic target molecules expressed in microglia cells are discussed.Entities:
Keywords: Amyloid hypothesis; Clinical studies; Dementia; Immunotherapy; Secretases
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Year: 2019 PMID: 31243509 DOI: 10.1007/s00115-019-0751-1
Source DB: PubMed Journal: Nervenarzt ISSN: 0028-2804 Impact factor: 1.214