Identification of biomarkers and immune infiltration characterization of lipid metabolism-associated genes in
Yuanye Ma1, Yang Liu1, Dan Luo2
1Department of Orthopedics, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao 266003, China.
Aging
|April 18, 2024
Summary
This study identifies key lipid metabolism genes linked to osteoarthritis (OA) pathogenesis using machine learning. These biomarkers show diagnostic potential and reveal connections between immune cells and metabolic dysfunction in OA patients.
Area of Science:
- Biochemistry
- Genetics
- Immunology
Background:
- Osteoarthritis (OA) is a widespread degenerative joint disease causing significant disability, particularly in older adults.
- Current OA treatments are limited, and its underlying pathogenesis, especially the role of metabolic processes, remains poorly understood.
Purpose of the Study:
- To investigate the role of lipid metabolism-associated genes (LAGs) in osteoarthritis (OA) pathogenesis.
- To identify potential diagnostic biomarkers for OA based on LAGs.
- To explore the relationship between immune infiltration and LAGs in OA.
Main Methods:
- Utilized public databases and machine learning algorithms (WGCNA, LASSO, RF).
- Performed immune infiltration analysis and pathway enrichment analysis.
- Conducted in vitro experiments: qRT-PCR, Western blot, lipid droplet analysis, and mitochondrial fatty acid oxidation assays.
Main Results:
- Identified three novel biomarkers associated with lipid metabolism in OA.
- Evaluated the diagnostic value of these biomarkers in OA patients.
- Found significant correlations between immune cell infiltration and the identified biomarkers.
- Verified abnormal LAG expression and confirmed the link between lipid metabolism and OA in vitro.
Conclusions:
- Lipid metabolism plays a crucial role in OA pathogenesis.
- The identified LAGs serve as potential diagnostic biomarkers for OA.
- Immune cell infiltration is intricately linked with metabolic dysregulation in OA, suggesting novel therapeutic targets.


