Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Aug;20(4):355-63.
doi: 10.1089/ten.TEB.2013.0377. Epub 2013 Dec 11.

The roles of catabolic factors in the development of osteoarthritis

Affiliations
Review

The roles of catabolic factors in the development of osteoarthritis

Dominick J Blasioli et al. Tissue Eng Part B Rev. 2014 Aug.

Abstract

Osteoarthritis (OA) is the most prevalent disease of articular joints characterized by joint space narrowing on X-ray, joint pain, and a loss of joint function through progressive cartilage degradation and intermittent synovial inflammation. Current in vitro models of OA are often monolayer cultured primary cells exposed to high concentrations of cytokines or chemokines, usually IL-1β or TNF-α. IL-1β could play a role in the early progression or even initiation of OA as evidenced by many of the in vitro studies. However, the inconsistent or outright lack of detectable IL-1β combined with high concentrations of the natural inhibitor IL-1Ra in the OA synovial fluid makes the idea of OA being IL-1β-driven questionable. Further, other stimulants, including IL-6 and matrix fragments, have been shown in vitro to cause many of the effects seen in OA at relevant concentrations found in the OA synovial fluid. More work with these stimulants and IL-1β-independent models needs to be done. Concurrently, research should be conducted with patients with OA as early as possible in the progression of their disease to be able to potentially identify, target, and treat the initiation of the disease.

PubMed Disclaimer

Figures

<b>FIG. 1.</b>
FIG. 1.
Disease perpetuation, catabolic cycle. Disease initiation of clinical osteoarthritis (OA) is due to several possible causes, including trauma, poor alignment, or inflammation. After initiation, joints undergo a catabolic cycle as shown. This catabolic cycle includes synovitis, pain, increases in proinflammatory cytokines and degradative enzymes, and extracellular matrix degeneration. Interrupting this cycle is likely essential to slowing the progression of OA.

Similar articles

Cited by

References

    1. Lawrence R.C., Felson D.T., Helmick C.G., Arnold L.M., Choi H., Deyo R.A., et al. . Estimates of the prevalence of arthritis and other rheumatic conditions in the United States. Arthritis Rheum 58,26, 2008 - PMC - PubMed
    1. Otterness I.G., Sindell A.C., Zimmerer R.O., Poole A.R., Ionescu M., and Weiner E.An analysis of 14 molecular markers for monitoring osteoarthritis: segregation of the markers into clusters and distinguishing osteoarthritis at baseline. Osteoarthritis Cartilage 8,180, 2000 - PubMed
    1. Malemud C.J., Martel-Pelletier J., and Pelletier J.P.Degradation of extracellular matrix in osteoarthritis: 4 fundamental questions. J Rheumatol 14,20, 1987 - PubMed
    1. Recommendations for the medical management of osteoarthritis of the hip and knee. 2000 update. American College of Rheumatology Subcommittee on Osteoarthritis Guidelines. Arthritis Rheum 43,1905, 2000 - PubMed
    1. Zhang W., Moskowitz R.W., Nuki G., et al. . OARSI recommendations for the management of hip and knee osteoarthritis, part II: OARSI evidence-based, expert consensus guidelines. Osteoarthritis Cartilage 16,137, 2008 - PubMed

Publication types

MeSH terms

LinkOut - more resources