# Characterization of gene expression profiles in Alzheimer’s disease and osteoarthritis: A bioinformatics study

## TL;DR

This study identifies shared gene expression patterns in Alzheimer's disease and osteoarthritis, suggesting common molecular mechanisms and potential therapeutic targets.

## Contribution

The study identifies key genes (EFEMP2, GABARAPL1, TSPO) as potential shared biomarkers and therapeutic targets for Alzheimer’s disease and osteoarthritis.

## Key findings

- EFEMP2 and TSPO are downregulated in both Alzheimer’s disease and osteoarthritis.
- GABARAPL1 is upregulated in both conditions, suggesting a role in autophagosome maturation.
- The identified genes show potential as diagnostic biomarkers and therapeutic targets.

## Abstract

Alzheimer’s disease (AD) and Osteoarthritis (OA) have been shown to have a close association in previous studies, but the pathogenesis of both diseases are unclear. This study explores the potential common molecular mechanisms between AD and OA through bioinformatics analysis, providing new insights for clinical treatment strategies.

The AD and OA-related datasets were downloaded from the gene expression database GEO. The datasets were analyzed to obtain differentially expressed gene (DEG) datasets for OA and AD, respectively. The intersection of these DEGs was analyzed to identify common DEGs (Co-DEGs). Subsequently, the Co-DEGs were enriched, and a protein-protein interaction network was constructed to identify core genes. The expression of these genes was validated in a separate dataset, and their diagnostic value for the diseases was analyzed. In addition, the core genes were analyzed using gene set enrichment analysis and single-gene genome variation analysis.

Analysis of DEGs on gene chips from OA and AD patients revealed significant changes in gene expression patterns. Notably, EFEMP2 and TSPO, genes associated with inflammatory responses, showed lower expression levels in both AD and OA patients, suggesting a downregulation in the pathological backgrounds of these diseases. Additionally, GABARAPL1, which is crucial for the maturation of autophagosomes, was found to be upregulated in both conditions. These findings suggest the potential of these genes as diagnostic biomarkers and potential therapeutic targets. However, to confirm the effectiveness of these genes as therapeutic targets, more in-depth mechanistic studies are needed in the future, particularly to explore the feasibility and specific mechanisms of combating disease progression by regulating the expression of these genes.

This study suggests that AD and OA shares common molecular mechanisms. The identification of EFEMP2, GABARAPL1, and TSPO as key target genes highlights potential common factors in both diseases. Further investigation into these findings could lead to new candidate targets and treatment directions for AD and OA, offering promising avenues for developing more effective and targeted therapeutic interventions.