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Rheumatoid Arthritis and Fibromyalgia Syndrome: A Bibliometric and Bioinformatics Perspective on Comorbidity Research
Guangyao Chen1,2, Zeran Yan1,2, Yifei Wang3
1Department of TCM Rheumatology, China-Japan Friendship Hospital, Beijing, 100029, People's Republic of China.
Research on rheumatoid arthritis (RA) and fibromyalgia syndrome (FMS) comorbidity is limited. Future studies should focus on neuroimmune regulation and inflammation-pain pathways for a unified framework.
Area of Science:
- Rheumatology and Pain Medicine
- Bioinformatics and Computational Biology
Background:
- Rheumatoid arthritis (RA) and fibromyalgia syndrome (FMS) are prevalent chronic pain conditions with complex diagnostic and treatment challenges.
- Systematic reviews on the pathological mechanisms, epidemiology, and research trends of RA-FMS comorbidity are lacking.
Purpose of the Study:
- To systematically review and analyze the research dynamics and knowledge structure of RA-FMS comorbidity.
- To explore the underlying genetic and molecular mechanisms of RA-FMS comorbidity.
Main Methods:
- Bibliometric analysis of 760 articles published between 2015 and 2024 from the Web of Science database.
- Co-occurrence and clustering analyses of countries, institutions, authors, journals, and keywords using VOSviewer and CiteSpace.
- Identification of shared genes and exploration of molecular mechanisms using GeneCards, PPI, and KEGG analyses.
Main Results:
- The United States leads in publication output, with the University of Michigan and Karolinska Institute as leading institutions.
- Daniel J. Clauw is the most prolific and cited author, and research predominantly focuses on clinical aspects.
- Analysis identified 216 overlapping genes and suggested roles for inflammatory reactions and neuroactive ligand-receptor interactions in comorbidity.
Conclusions:
- Current research on RA-FMS comorbidity requires greater depth in mechanistic understanding.
- Future research should prioritize interdisciplinary collaboration to investigate neuroimmune regulation, central sensitization, and inflammation-pain pathways.
- Establishing a unified comorbidity framework for RA-FMS is essential.
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