Omics-driven insights into the molecular pathways driving osteoarthritis pathogenesis
Paco Mattheus Jacobus Welsing1, Said El Bouhaddani2, Lin Zhu3
1Department of Rheumatology and Clinical Immunology, University Medical Center, Utrecht, The Netherlands.
Connective Tissue Research
|September 8, 2025
Summary
Advanced omics studies in osteoarthritis (OA) reveal molecular subtypes but lack direct therapeutic impact. Future research integrating AI and spatial omics may enable personalized OA treatments and disease modification.
Area of Science:
- Biomedical Research
- Genomics and Molecular Biology
- Rheumatology
Background:
- Osteoarthritis (OA) is a prevalent joint disorder with no approved disease-modifying treatments.
- Current understanding of OA pathogenesis is limited despite its significant impact on quality of life.
Purpose of the Study:
- To review single- and multi-omics studies in OA.
- To highlight the role of omics in identifying molecular and therapeutic subtypes.
- To discuss challenges and future directions for omics-driven OA research.
Main Methods:
- Review of genomics, transcriptomics, proteomics, and metabolomics studies in OA.
- Analysis of multi-omics integration and spatial proteomics findings.
- Discussion of challenges including data complexity and translational validation.
Main Results:
- Omics technologies have advanced understanding of OA pathogenesis and molecular pathways.
- Multi-omics integration reveals crosstalk between inflammatory, metabolic, and degradative processes.
- Spatial proteomics offers insights into synovial tissue heterogeneity.
Conclusions:
- Omics research has yet to yield effective disease-modifying OA therapies.
- Future work should integrate AI, single-cell, and spatial omics in longitudinal studies.
- Addressing current challenges can lead to personalized OA therapies and improved patient differentiation, including distinguishing OA from psoriatic arthritis (PsA).
Related Concept Videos
The JAK-STAT Signaling Pathway
12.2K
Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as SH2...
12.2K
Genome-wide Association Studies-GWAS
15.3K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
15.3K
Osteoclasts in Bone Remodeling
3.9K
Osteoclasts are cells responsible for bone resorption and remodeling. They originate from hematopoietic progenitor cells present in the bone marrow. Numerous progenitor cells fuse to form multinucleated cells, each with 10-20 nuclei. A single osteoclast has a diameter of 150 to 200 µM. These cells have ruffled borders that break down the underlying bone tissue and release minerals such as calcium into the blood in bone resorption. Osteoclasts cling to bones with their ruffled edges during...
3.9K


