| Literature DB >> 33589615 |
Steve Rodriguez1,2, Clemens Hug1, Petar Todorov1, Nienke Moret1, Sarah A Boswell1, Kyle Evans1,2, George Zhou1,2, Nathan T Johnson1, Bradley T Hyman2, Peter K Sorger1, Mark W Albers3,4, Artem Sokolov5.
Abstract
Clinical trials of novel therapeutics for Alzheimer's Disease (AD) have consumed a large amount of time and resources with largely negative results. Repurposing drugs already approved by the Food and Drug Administration (FDA) for another indication is a more rapid and less expensive option. We present DRIAD (Drug Repurposing In AD), a machine learning framework that quantifies potential associations between the pathology of AD severity (the Braak stage) and molecular mechanisms as encoded in lists of gene names. DRIAD is applied to lists of genes arising from perturbations in differentiated human neural cell cultures by 80 FDA-approved and clinically tested drugs, producing a ranked list of possible repurposing candidates. Top-scoring drugs are inspected for common trends among their targets. We propose that the DRIAD method can be used to nominate drugs that, after additional validation and identification of relevant pharmacodynamic biomarker(s), could be readily evaluated in a clinical trial.Entities:
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Year: 2021 PMID: 33589615 DOI: 10.1038/s41467-021-21330-0
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919