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Periprosthetic inflammation: From the cellular level to clinical implications

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F25%3A00142267" target="_blank" >RIV/00216224:14110/25:00142267 - isvavai.cz</a>

  • Result on the web

    <a href="https://academic.oup.com/jbmrplus/advance-article/doi/10.1093/jbmrpl/ziaf154/8257522" target="_blank" >https://academic.oup.com/jbmrplus/advance-article/doi/10.1093/jbmrpl/ziaf154/8257522</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1093/jbmrpl/ziaf154" target="_blank" >10.1093/jbmrpl/ziaf154</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Periprosthetic inflammation: From the cellular level to clinical implications

  • Original language description

    Periprosthetic inflammation is a crucial factor contributing to aseptic loosening, the leading cause of implant failures. Metallic debris, including nanoparticles, sub-micron particles, and ions, plays a central role in triggering inflammatory responses around orthopaedic implants. Exposure to the debris activates macrophages via Toll-like receptors (TLRs) and NOD-like receptors (NLRs), which in turn leads to the production of pro-inflammatory cytokines. This signalling cascade subsequently drives osteoclast activation, resulting in periprosthetic bone loss and, ultimately, implant loosening. Recent research has focused on strategies to prevent aseptic loosening by targeting the inflammation induced by metallic particles/ions. Pharmacological interventions aimed at modulating macrophage activation and inhibiting specific inflammatory pathways have shown promise in reducing osteoclast activity and excessive bone resorption. This review provides a comprehensive overview of the processes involved in the pathogenesis of periprosthetic inflammation, beginning with the release of metallic debris and its recognition by immune cells, followed by the inflammatory reactions that lead to osteoclastogenesis and bone loss. A detailed understanding of these molecular mechanisms is essential for the development of targeted approaches to prevent aseptic loosening, improve long-term patient outcomes, and alleviate the economic burden on healthcare systems.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30211 - Orthopaedics

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    JBMR PLUS

  • ISSN

    2473-4039

  • e-ISSN

    2473-4039

  • Volume of the periodical

    9

  • Issue of the periodical within the volume

    11

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    14

  • Pages from-to

    1-14

  • UT code for WoS article

    001593825900001

  • EID of the result in the Scopus database

    2-s2.0-105019528592