| Literature DB >> 32472577 |
Jennifer Cable1, David M Holtzman2, Bradley T Hyman3, Malú Gámez Tansey4, Marco Colonna5, Manolis Kellis6,7, Roberta D Brinton8, Marilyn Albert9, Cheryl L Wellington10, Sangram S Sisodia11,12, Rudolph E Tanzi13.
Abstract
For decades, Alzheimer's disease research has focused on amyloid as the primary pathogenic agent. This focus has driven the development of numerous amyloid-targeting therapies; however, with one possible exception, none of these therapies have been effective in preventing or delaying cognitive decline in patients, and there are no approved disease-modifying agents. It is becoming more apparent that alternative drug targets are needed to address this complex disease. An increased understanding of Alzheimer's disease pathology has highlighted the need to target the appropriate disease pathology at the appropriate time in the disease course. Preclinical and early clinical studies have focused on targets, including inflammation, tau, vascular health, and the microbiome. This report summarizes the presentations from a New York Academy of Sciences' one-day symposium entitled "Alzheimer's Disease Therapeutics: Alternatives to Amyloid," held on November 20, 2019.Entities:
Keywords: APOE; Alzheimer's disease; HDL; TREM2; allopregnanolone; amyloid; cognitive impairment; dementia; microbiome; microglia; neuroinflammation; tau
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Year: 2020 PMID: 32472577 DOI: 10.1111/nyas.14371
Source DB: PubMed Journal: Ann N Y Acad Sci ISSN: 0077-8923 Impact factor: 5.691