The Role of Receptor Activator of Nuclear Factor-κB Ligand/Osteoprotegerin Ratio in Synovial Fluid as a Potential Marker for Periprosthetic Osteolysis Following Total Ankle Arthroplasty.


Journal

Clinics in orthopedic surgery
ISSN: 2005-4408
Titre abrégé: Clin Orthop Surg
Pays: Korea (South)
ID NLM: 101505087

Informations de publication

Date de publication:
Aug 2024
Historique:
received: 19 12 2023
revised: 26 01 2024
accepted: 26 01 2024
medline: 2 8 2024
pubmed: 2 8 2024
entrez: 2 8 2024
Statut: ppublish

Résumé

Periprosthetic osteolysis is a prevalent complication following total ankle arthroplasty (TAA), implicating various cytokines in osteoclastogenesis as pivotal in this process. This study aimed to evaluate the relationship between osteolysis and the concentrations of osteoclastogenesis-related cytokines in synovial fluid and investigate its clinical value following TAA. Synovial fluid samples from 23 ankles that underwent revision surgery for osteolysis following TAA were analyzed as the osteolysis group. As a control group, we included synovial fluid samples obtained from 23 ankles during primary TAA for osteoarthritis. The receptor activator of nuclear factor-κB ligand (RANKL)/osteoprotegerin (OPG) ratio in these samples was quantified using sandwich enzyme-linked immunosorbent assay techniques, and a bead-based multiplex immunoassay facilitated the detection of specific osteoclastogenesis-related cytokines. RANKL levels averaged 487.9 pg/mL in 14 of 23 patients in the osteolysis group, with no detection in the control group's synovial fluid. Conversely, a significant reduction in OPG levels was observed in the osteolysis group ( Our results demonstrated that periprosthetic osteolysis was associated with osteoclastogenesis activation through an elevated RANKL/OPG ratio following TAA. We assume that RANKL and other osteoclastogenesis-related cytokines in the synovial fluid have clinical value as a potential marker for the development and progression of osteolysis following TAA.

Sections du résumé

Background UNASSIGNED
Periprosthetic osteolysis is a prevalent complication following total ankle arthroplasty (TAA), implicating various cytokines in osteoclastogenesis as pivotal in this process. This study aimed to evaluate the relationship between osteolysis and the concentrations of osteoclastogenesis-related cytokines in synovial fluid and investigate its clinical value following TAA.
Methods UNASSIGNED
Synovial fluid samples from 23 ankles that underwent revision surgery for osteolysis following TAA were analyzed as the osteolysis group. As a control group, we included synovial fluid samples obtained from 23 ankles during primary TAA for osteoarthritis. The receptor activator of nuclear factor-κB ligand (RANKL)/osteoprotegerin (OPG) ratio in these samples was quantified using sandwich enzyme-linked immunosorbent assay techniques, and a bead-based multiplex immunoassay facilitated the detection of specific osteoclastogenesis-related cytokines.
Results UNASSIGNED
RANKL levels averaged 487.9 pg/mL in 14 of 23 patients in the osteolysis group, with no detection in the control group's synovial fluid. Conversely, a significant reduction in OPG levels was observed in the osteolysis group (
Conclusions UNASSIGNED
Our results demonstrated that periprosthetic osteolysis was associated with osteoclastogenesis activation through an elevated RANKL/OPG ratio following TAA. We assume that RANKL and other osteoclastogenesis-related cytokines in the synovial fluid have clinical value as a potential marker for the development and progression of osteolysis following TAA.

Identifiants

pubmed: 39092303
doi: 10.4055/cios23411
pmc: PMC11262952
doi:

Substances chimiques

RANK Ligand 0
Osteoprotegerin 0
Biomarkers 0
TNFSF11 protein, human 0
Cytokines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

661-668

Informations de copyright

Copyright © 2024 by The Korean Orthopaedic Association.

Déclaration de conflit d'intérêts

CONFLICT OF INTEREST: No potential conflict of interest relevant to this article was reported.

Auteurs

Gun-Woo Lee (GW)

Department of Orthopedic Surgery, Chonnam National University Hospital, Gwangju, Korea.
Department of Orthopedic Surgery, Chonnam National University Medical School, Gwangju, Korea.

Ji-Eun Song (JE)

Department of Orthopedic Surgery, Chonnam National University Hospital, Gwangju, Korea.

Jeong-Eun Han (JE)

Department of Orthopedic Surgery, Chonnam National University Hospital, Gwangju, Korea.

Nack-Sung Kim (NS)

Department of Pharmacology, Chonnam National University Medical School, Gwangju, Korea.

Keun-Bae Lee (KB)

Department of Orthopedic Surgery, Chonnam National University Hospital, Gwangju, Korea.
Department of Orthopedic Surgery, Chonnam National University Medical School, Gwangju, Korea.

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Classifications MeSH