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
. 2025 Jun 5:16:1593658.
doi: 10.3389/fendo.2025.1593658. eCollection 2025.

Association of organs-crosstalk with the pathogenesis of osteoarthritis: cartilage as a key player

Affiliations
Review

Association of organs-crosstalk with the pathogenesis of osteoarthritis: cartilage as a key player

Yingda Qin et al. Front Endocrinol (Lausanne). .

Abstract

Degeneration of articular cartilage is the hallmark pathologic change in osteoarthritis (OA). Cartilage not only serves as a shock-absorbing structure for movement but is also regulated by organs other than bone, while chondrocytes secrete cytokines that influence these organs. The concept of organ axis refers to the regulatory pathways formed between organs via cytokine signaling. The communication network established between cartilage and other organs constitutes the cartilage-organ axis. Through this axis, these organs regulate articular chondrocyte proliferation and apoptosis. It is evident that chondrocytes play a central role in connecting various organs to the progression of OA, prompting interest in strategies to intervene in cartilage damage by modulating the organ axis. This review presents, for the first time, a system summarizing the effects of the extraosseous system on cartilage through various factors that alter OA progression. The aim is to fully elucidate the effects of different organs on cartilage, thus providing insights into the treatment of OA and systemic diseases.

Keywords: cartilage; chondrocyte; organs-crosstalk; osteoarthritis; therapeutic strategy.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Cartilage is affected by organs throughout the body and also affects some of the organs.
Figure 2
Figure 2
Overview of interaction between cartilage and brain, heart, lungs and liver.
Figure 3
Figure 3
Overview of Intestinal, renal, gonadal, pancreatic, adipose, muscular, and skeletal effects on cartilage.

Similar articles

References

    1. Global incidence, prevalence, years lived with disability (YLDs), disability-adjusted life-years (DALYs), and healthy life expectancy (HALE) for 371 diseases and injuries in 204 countries and territories and 811 subnational locations, 1990-2021: a systematic analysis for the Global Burden of Disease Study 2021. Lancet (London England). (2024) 403:2133–61. doi: 10.1016/S0140-6736(24)00757-8 - DOI - PMC - PubMed
    1. Park JH, Hong JY, Han K, Suh SW, Park SY, Yang JH, et al. Prevalence of symptomatic hip, knee, and spine osteoarthritis nationwide health survey analysis of an elderly Korean population. Med (Baltimore). (2017) 96:e6372. doi: 10.1097/MD.0000000000006372 - DOI - PMC - PubMed
    1. Dasa V, Mihalko W, Rivadeneyra A, Urban J, Wickline A, Rogenmoser D, et al. Innovations in Genicular Outcomes Registry (IGOR): protocol for a real-world registry study of treatments for knee osteoarthritis. Ther Adv musculoskel Dis. (2024) 16:1759720x241304193. doi: 10.1177/1759720X241304193 - DOI - PMC - PubMed
    1. Courties A, Kouki I, Soliman N, Mathieu S, Sellam J. Osteoarthritis year in review 2024: Epidemiology and therapy. Osteoarthr cartil. (2024) 32:1397–404. doi: 10.1016/j.joca.2024.07.014 - DOI - PubMed
    1. Ren J-L, Yang J, Hu W. The global burden of osteoarthritis knee: a secondary data analysis of a population-based study. Clin Rheumatol. (2025) 44(4):1769–810. doi: 10.1007/s10067-025-07347-6 - DOI - PMC - PubMed

LinkOut - more resources