# Integrative clinical and molecular insights into the comorbidity between depression and sleep apnea syndrome

## TL;DR

This study finds a strong link between depression and sleep apnea syndrome, showing they share genes and biological pathways that could lead to better treatments.

## Contribution

The study identifies shared genes and pathways between depression and sleep apnea using AI-driven analysis and clinical data.

## Key findings

- 62.07% of sleep apnea patients showed depressive symptoms with mild to moderate severity.
- 872 genes were shared between depression and sleep apnea, with 24 key genes forming a densely connected network.
- Shared pathways include oxidative stress, ferroptosis, and inflammation, with MIF and SOD2 as key regulators.

## Abstract

To identify and characterize overlapping genes and pathways linking Depression and Sleep Apnea Syndrome (SAS).

A three-level analysis was conducted. Clinically, depression severity in 29 SAS patients was assessed using the Zung Self-Rating Depression Scale. Molecularly, an AI-driven literature mining approach was applied to extract gene–disease associations from PubMed and bioinformatics databases (19,924 genes), with prioritization using the Adjusted Binomial Method and validation via differential expression analysis. Functionally, shared genes were explored through protein–protein interaction (PPI) networks, enrichment analysis, and directional pathway modeling.

Clinically, 62.07% of SAS patients exhibited depressive symptoms, with mild to moderate severity based on the Zung Self-Rating Depression Scale. Molecularly, 872 genes were found to be shared between 4,544 Depression-related and 1,197 SAS-related genes (OR = 11; p = 4.95 × 10-319). Further prioritization identified 24 overlapping genes with strong enrichment (OR = 10.9; p = 3.32 × 10-16), supported by validation in multiple gene expression datasets. These genes formed a densely connected protein–protein interaction network (238 edges; density = 0.43; clustering coefficient = 0.87), with core hubs including CASP3, TP53, SOD2, HMOX1, and MIR146A. Enrichment analysis highlighted involvement in oxidative stress, ferroptosis, and inflammatory pathways. Directional pathway modeling indicated that SAS may influence Depression via 18 genes and vice versa via 5 genes, with MIF and SOD2 acting as shared regulators.

This study reveals significant clinical and molecular links between Depression and SAS, identifying shared biological pathways and candidate targets for integrated therapeutic strategies.