Machine learning identifies candidates for drug repurposing in Alzheimer’s disease

Steve Rodriguez, Clemens B. Hug, Petar V. Todorov, Nienke Moret, Sarah A. Boswell, Kyle E. Evans, George Zhou, Nathan T. Johnson et al.

Nature Communications 2021 article cited by 293

importance 7/10 ai assisted Computational Drug Discovery Methods drug repurposing stage: research

Alzheimer's disease drug trials are slow, expensive and largely failing, so existing approved drugs need to be screened for reuse.

Alzheimer's affects millions with no effective treatment, and repurposing approved drugs is faster and cheaper than new drug development.

The DRIAD machine learning framework quantifies associations between AD pathology severity (Braak stage) and gene lists, then ranked 80 FDA-approved drugs as repurposing candidates.

Validated on known AD-associated gene lists; produced ranked list of repurposing candidates from 80 FDA-approved drugs.

ML prioritized approved drugs for Alzheimer's repurposing, but no clinical efficacy is demonstrated in the abstract.

Venue Nature Communications
Published 2021
Work type article
Authors Steve Rodriguez, Clemens B. Hug, Petar V. Todorov, Nienke Moret, Sarah A. Boswell, Kyle E. Evans, George Zhou, Nathan T. Johnson et al.
Citations 293 (OpenAlex, at import time)
References 95
Model or method DRIAD
Organization not stated in source
Primary source https://doi.org/10.1038/s41467-021-21330-0
Open access gold
Keywords drug repurposing, Alzheimer's disease, machine learning, DRIAD, Braak stage, FDA-approved drugs
7 / 10

significant — thousands to millions affected

AD trials have consumed large time/resources with largely negative results; repurposing 80 FDA-approved drugs offers faster, cheaper path, but abstract states no affected-population scale or clinical efficacy.

Basis: inferred. Judged from the source text, which gives no explicit scale. Stated scale: not stated in source. Method and limits.

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