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Screening and Verification COPD-OSA Overlap Syndrome Core Genes Using Bioinformatics.
Shihao Qiang1, Rongrong Wan1, Jingyi Wu1
1Department of General Medicine, The Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi Medical Center, Nanjing Medical University, Wuxi People's Hospital, Wuxi, Jiangsu Province, 214023, People's Republic of China.
Overlap syndrome (OS), a condition where obstructive sleep apnea (OSA) and chronic obstructive pulmonary disease (COPD) coexist, has unclear molecular mechanisms. Bioinformatics analysis identified GRM8 as a key downregulated gene in OS, offering new research directions.
Area of Science:
- Pulmonary Medicine
- Genetics
- Bioinformatics
Background:
- Overlap syndrome (OS) involves the coexistence of obstructive sleep apnea (OSA) and chronic obstructive pulmonary disease (COPD).
- The underlying molecular mechanisms of OS remain largely unknown.
- This study employed bioinformatics to investigate potential molecular mechanisms of OS.
Purpose of the Study:
- To identify common differentially expressed genes (DEGs) in OSA and COPD.
- To uncover key genes and molecular pathways associated with OS using bioinformatics.
- To validate potential diagnostic or mechanistic biomarkers for OS.
Main Methods:
- Acquired gene expression datasets for OSA and COPD from the Gene Expression Omnibus (GEO) database.
- Performed differential gene expression analysis and Weighted Gene Co-expression Network Analysis (WGCNA).
- Validated identified key genes, including GRM8, using external datasets and RT-qPCR.
Main Results:
- Identified 9 common DEGs and 128 common key module genes between OSA and COPD.
- Determined 5 key genes by intersecting DEG and WGCNA results.
- Found GRM8 significantly downregulated in COPD and OS patients compared to controls, with high diagnostic value (AUC=0.857).
Conclusions:
- Identified GRM8 as a potential hub gene significantly associated with OS.
- The findings provide novel insights into the molecular mechanisms of OS.
- GRM8 may serve as a potential biomarker and therapeutic target for OS.
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