Most recent developments in strategies to reduce the progression of structural changes in osteoarthritis: today and tomorrow
- PMID: 16569256
- PMCID: PMC1526599
- DOI: 10.1186/ar1932
Most recent developments in strategies to reduce the progression of structural changes in osteoarthritis: today and tomorrow
Abstract
Osteoarthritis (OA), the most common of all arthritic conditions, is a social and financial burden to all nations. The most recent research has significantly advanced our understanding of the cause of OA and risk factors associated with it. These findings have provided useful information that has helped in the daily management of patients with OA. Some preventative measures and a number of therapeutic agents and drugs are available, which may help to reduce the progression of OA in certain patients. Moreover, the most recent progress in research has significantly enhanced our knowledge of the factors involved in the development of the disease and of the mechanisms responsible for its progression. This has allowed identification of several new therapeutic targets in a number of pathophysiological pathways. Consequently, the field is opening up to a new era in which drugs and agents that can specifically block important mechanisms responsible for the structural changes that occur in OA can be brought into development and eventually into clinical trials.
Similar articles
-
DMOAD developments: present and future.Bull NYU Hosp Jt Dis. 2007;65(3):242-8. Bull NYU Hosp Jt Dis. 2007. PMID: 17922676 Review.
-
Emerging pathways and promising agents with possible disease modifying effect in osteoarthritis treatment.Curr Drug Targets. 2014 Jun;15(6):635-61. doi: 10.2174/1389450115666140306153115. Curr Drug Targets. 2014. PMID: 24597569
-
New horizons in osteoarthritis.Swiss Med Wkly. 2010 Sep 17;140:w13098. doi: 10.4414/smw.2010.13098. eCollection 2010. Swiss Med Wkly. 2010. PMID: 20458653 Review.
-
Osteoarthritis research priorities: a report from a EULAR ad hoc expert committee.Ann Rheum Dis. 2014 Aug;73(8):1442-5. doi: 10.1136/annrheumdis-2013-204660. Epub 2014 Mar 13. Ann Rheum Dis. 2014. PMID: 24625626
-
Rationale for the use of structure-modifying drugs and agents in the treatment of osteoarthritis.Osteoarthritis Cartilage. 2004;12 Suppl A:S63-8. doi: 10.1016/j.joca.2003.09.014. Osteoarthritis Cartilage. 2004. PMID: 14698646
Cited by
-
Alterative effects of an oral alginate extract on experimental rabbit osteoarthritis.J Biomed Sci. 2015 Aug 4;22(1):64. doi: 10.1186/s12929-015-0169-4. J Biomed Sci. 2015. PMID: 26239837 Free PMC article.
-
Machine learning-based prediction of knee pain risk using lipid metabolism biomarkers: a prospective cohort study from CHARLS.Front Physiol. 2025 Jun 25;16:1607276. doi: 10.3389/fphys.2025.1607276. eCollection 2025. Front Physiol. 2025. PMID: 40636147 Free PMC article.
-
Intra-articular hylastan versus steroid for knee osteoarthritis.Knee Surg Sports Traumatol Arthrosc. 2014 Jul;22(7):1684-92. doi: 10.1007/s00167-013-2438-7. Epub 2013 Feb 16. Knee Surg Sports Traumatol Arthrosc. 2014. PMID: 23417236 Clinical Trial.
-
Comparison of the effectiveness of intra-infrapatellar fat pad and intra-articular glucocorticoid injection in knee osteoarthritis patients with Hoffa's synovitis: protocol for a multicentre randomised controlled trial.BMJ Open. 2025 Jan 28;15(1):e087785. doi: 10.1136/bmjopen-2024-087785. BMJ Open. 2025. PMID: 39880431 Free PMC article.
-
Anti-inflammatory strategies in cartilage repair.Tissue Eng Part B Rev. 2014 Dec;20(6):655-68. doi: 10.1089/ten.TEB.2014.0014. Epub 2014 Jun 23. Tissue Eng Part B Rev. 2014. PMID: 24846478 Free PMC article. Review.
References
-
- Lajeunesse D, Pelletier JP, Martel-Pelletier J. Osteoarthritis: a metabolic disease induced by local abnormal leptin activity? Curr Rheumatol Rep. 2005;7:79–81. - PubMed
-
- Lajeunesse D, Delalandre A, Fernandes J. Subchondral osteoblasts from osteoarthritic patients show abnormal expression and production of leptin: possible role in cartilage degradation [Abstract] J Bone Miner Res. 2004;19:S149.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical