# Genetic and Pathogenic Overlaps Between Autism Spectrum Disorder and Alzheimer’s Disease: Evolutionary Features and Opportunities for Drug Repurposing

**Authors:** Ekaterina A. Trifonova, Anna A. Pashchenko, Roman A. Ivanov, Alex V. Kochetov, Sergey A. Lashin

PMC · DOI: 10.3390/ijms262010066 · International Journal of Molecular Sciences · 2025-10-16

## TL;DR

This study explores genetic and evolutionary links between autism and Alzheimer's, identifying shared mTOR pathway genes and potential drug repurposing opportunities.

## Contribution

The study reveals evolutionary features and drug repurposing opportunities by analyzing gene networks and phylogenetic patterns in ASD and AD.

## Key findings

- Nearly half of ASD and two-fifths of AD predisposition genes are linked to the mTOR signaling pathway.
- ASD and AD gene sets show significant enrichment of evolutionarily ancient genes.
- Potential drugs for ASD treatment include propofol, dexamethasone, and natural compounds like resveratrol and quercetin.

## Abstract

Autism spectrum disorder (ASD) and Alzheimer’s disease (AD) are neurodevelopmental and neurodegenerative disorders, respectively. While exome sequencing is routinely employed during the early stages of ASD diagnosis, it rarely influences therapeutic strategies. To address this gap, we have reconstructed and analyzed the gene networks linking autism spectrum disorders, Alzheimer’s disease, and mTOR signaling. In addition, we have performed a phylostratigraphic analysis that reveals similarities and differences in the evolution of both ASD and Alzheimer’s disease predisposition genes. We have shown that almost half of the genes predisposing to autism and two-fifths of the genes predisposing to Alzheimer’s disease are directly related to the mTOR signaling pathway. Analysis of Phylostratigraphic Age Index (PAI) value distributions revealed a significant enrichment of evolutionarily ancient genes in both ASD- and AD-related gene sets. When studying the distribution of ASD predisposition genes by Divergence Index (DI) values, a significant enrichment with genes having extremely low DI = 0 has been found. Such low DI values indicate that most likely these genes are under stabilizing selection. Using the ANDVisio tool, both pharmacological and natural mTOR regulators with potential for ASD treatment were selected, such as propofol, dexamethasone, celecoxib, statins, berberine, resveratrol, quercetin, myricetin, mio-inositol, and several amino acids.

## Linked entities

- **Chemicals:** propofol (PubChem CID 4943), dexamethasone (PubChem CID 5743), celecoxib (PubChem CID 2662), berberine (PubChem CID 2353), resveratrol (PubChem CID 5056), quercetin (PubChem CID 5280343), myricetin (PubChem CID 5281672)
- **Diseases:** autism spectrum disorder (MONDO:0005258), Alzheimer’s disease (MONDO:0004975)

## Full-text entities

- **Genes:** MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}
- **Diseases:** ASD (MESH:D000067877), autism (MESH:D001321), AD (MESH:D000544), neurodevelopmental and neurodegenerative disorders (MESH:D019636)
- **Chemicals:** propofol (MESH:D015742), dexamethasone (MESH:D003907), resveratrol (MESH:D000077185), mio-inositol (-), myricetin (MESH:C040015), quercetin (MESH:D011794), celecoxib (MESH:D000068579), berberine (MESH:D001599), amino acids (MESH:D000596)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12564320/full.md

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12564320/full.md

## References

66 references — full list in the complete paper: https://tomesphere.com/paper/PMC12564320/full.md

---
Source: https://tomesphere.com/paper/PMC12564320