Machine learning identifies candidates for drug repurposing in Alzheimer's disease.
Steve RodriguezClemens B HugPetar V TodorovNienke MoretSarah A BoswellKyle EvansGeorge ZhouNathan T JohnsonBradley T HymanPeter Karl SorgerMark W AlbersArtem SokolovPublished in: Nature communications (2021)
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.
Keyphrases
- drug administration
- clinical trial
- machine learning
- genome wide
- drug induced
- endothelial cells
- cognitive decline
- dna methylation
- stem cells
- genome wide identification
- deep learning
- study protocol
- mesenchymal stem cells
- risk assessment
- double blind
- transcription factor
- bone marrow
- quantum dots
- loop mediated isothermal amplification