Elevated secretion of pro-collagen I-alpha and vascular endothelial growth factor as biomarkers of acetabular labrum degeneration and calcification in hip osteoarthritis: An explant study.

Acetabular labrum Biomarker Explant model Hip osteoarthritis Inflammation Pathologic calcification

Journal

Journal of orthopaedic translation
ISSN: 2214-031X
Titre abrégé: J Orthop Translat
Pays: Singapore
ID NLM: 101625127

Informations de publication

Date de publication:
Jan 2024
Historique:
received: 03 02 2023
revised: 29 06 2023
accepted: 23 08 2023
medline: 5 1 2024
pubmed: 5 1 2024
entrez: 5 1 2024
Statut: epublish

Résumé

Hip osteoarthritis (OA) involves structural degeneration of different joint compartments, including femoral head cartilage, periarticular ligaments and the acetabular labrum. However, the molecular mechanisms underlying labrum degeneration in hip OA remain poorly understood. To assess secretion of putative biomarkers for OA from explanted human labrum tissues under basal and inflammatory conditions and to determine whether these could differentiate between OA and calcification status compared to fracture controls. Intact labrum specimens were collected from patients undergoing joint arthroplasty for primary hip OA ( Whole mount microscopy revealed non-OA fracture controls were non-calcified, whereas six OA labra (40%) were partially calcified or ossified. Basal secretion of Pro-Col-Iα and VEGF was increased four-fold in OA versus non-OA labra. Pro-Col-Iα levels were correlated with those of VEGF ( Secretion of the putative OA biomarkers Pro-Col-Iα and VEGF is elevated in degenerated human acetabular labrum and may serve as indicators of OA and calcification status. Secretion of both factors was partially regulated by TGF-beta signaling in calcified OA labrum tissues.

Sections du résumé

Background UNASSIGNED
Hip osteoarthritis (OA) involves structural degeneration of different joint compartments, including femoral head cartilage, periarticular ligaments and the acetabular labrum. However, the molecular mechanisms underlying labrum degeneration in hip OA remain poorly understood.
Aim UNASSIGNED
To assess secretion of putative biomarkers for OA from explanted human labrum tissues under basal and inflammatory conditions and to determine whether these could differentiate between OA and calcification status compared to fracture controls.
Methods UNASSIGNED
Intact labrum specimens were collected from patients undergoing joint arthroplasty for primary hip OA (
Results UNASSIGNED
Whole mount microscopy revealed non-OA fracture controls were non-calcified, whereas six OA labra (40%) were partially calcified or ossified. Basal secretion of Pro-Col-Iα and VEGF was increased four-fold in OA versus non-OA labra. Pro-Col-Iα levels were correlated with those of VEGF (
Conclusions UNASSIGNED
Secretion of the putative OA biomarkers Pro-Col-Iα and VEGF is elevated in degenerated human acetabular labrum and may serve as indicators of OA and calcification status. Secretion of both factors was partially regulated by TGF-beta signaling in calcified OA labrum tissues.

Identifiants

pubmed: 38179125
doi: 10.1016/j.jot.2023.08.007
pii: S2214-031X(23)00061-X
pmc: PMC10765489
doi:

Types de publication

Journal Article

Langues

eng

Pagination

19-25

Informations de copyright

© 2023 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no conflicts of interest related to this study.

Auteurs

Alexander Antoniadis (A)

Department of Orthopedics, Lausanne University Hospital and University of Lausanne, Switzerland.

Julien Wegrzyn (J)

Department of Orthopedics, Lausanne University Hospital and University of Lausanne, Switzerland.

Patrick Omoumi (P)

Department of Diagnostic and Interventional Radiology, Lausanne University Hospital and University of Lausanne, Switzerland.

Léa Loisay (L)

Department of Rheumatology, Lausanne University Hospital and University of Lausanne, Switzerland.

Thomas Hügle (T)

Department of Rheumatology, Lausanne University Hospital and University of Lausanne, Switzerland.

Jeroen Geurts (J)

Department of Rheumatology, Lausanne University Hospital and University of Lausanne, Switzerland.

Classifications MeSH