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Alzheimer's disease (AD) is a chronic neurodegenerative disease associated with progressive cognitive decline, extracellular amyloid plaques, intracellular neurofibrillary tangles, and neuronal death
GWAS
In fact, the U.
Administer FDA
The number of AD patients is projected to rise to 13.
Broadly defined disease, gene-supported drug targets have high success rates in FDA-approved therapies
To address this key issue in the field, they developed a web-based artificial intelligence framework capable of integrating multi-omics data as well as human protein-protein interactome networks to accurately infer GWAS-confirmed variants affected by Accurate drug targets to identify new treatments
Using this approach, they identified 103 AD ARGs that were validated by varying degrees of pathobiological evidence
In a retrospective case-control validation, pioglitazone use was significantly associated with a reduction in AD risk (hazard ratio (HR) = 0.
Pioglitazone, a peroxisome proliferator-activated receptor (PPAR) agonist for the treatment of type 2 diabetes , was demonstrated in a propensity-score-matched cohort study to be comparable to glipizide (HR = 0.
diabetes
In vitro experiments showed that pioglitazone down-regulated glycogen synthase 3β (GSK3β) and cyclin-dependent kinase (CDK5) in human microglia, supporting a possible mechanism of action for its beneficial effects on AD
Pioglitazone downregulates glycogen synthase 3β (GSK3β) and cyclin-dependent kinase (CDK5) in human microglia, supporting a possible mechanism of action for its beneficial effects on AD
An integrated, web-based artificial intelligence approach is proposed to rapidly translate GWAS findings and multi-omics data into genotype-informed therapeutic discovery for AD
Artificial intelligence framework identifies candidate targets for drug repurposing in Alzheimer's disease.
Alz Res Therapy.
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