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Degenerative changes of the interface membrane as a possible reason for prosthesis loosening.

Authors :
Krohmer G
Koleganova N
Hadjicostas PT
Fink B
Berger I
Source :
Histology and histopathology [Histol Histopathol] 2008 Aug; Vol. 23 (8), pp. 925-33.
Publication Year :
2008

Abstract

Objective: The aim of the present study was to perform a comparative evaluation of septic and aseptic interface membranes, assessing histological features, inflammatory infiltrate, and expression of inflammatory cytokines.<br />Methods: Septic and aseptic interface membranes from 102 patients were examined by histology, histochemistry, and immunohistochemistry (tissue arrays). The cell subpopulations were characterized by quantification of CD3, CD4, CD8, CD20, and CD163 positive cells. Additionally, a semiquantitative evaluation of inflammatory cytokines (TNFalpha, TGF-beta1, IL-1, IL-6, CRP, MMP-1, MMP-6) was performed to complete the analysis of inflammatory infiltrates.<br />Results: The histological analysis revealed three different types of aseptic interface membranes: wear particle, degenerative, and mixed type. The expression of inflammatory molecules did not differ between septic and wear particle interface membranes. Significantly lower expression of cytokines, MMPs and CRP was observed, however, in degenerative interface membranes compared to other types. No expression of TNFalpha was observed in the degenerative interface membranes. Over 88% of patients with degenerative interface membranes had had a clinical record of osteoarthritis.<br />Conclusion: Aseptic interface membranes were represented by wear particle, degenerative and mixed type. The expression of inflammatory factors in wear particle type is similar to this in septic membranes and can contribute to the bone destruction and prosthesis loosening. These factors seem not to play a major role in the degenerative membranes.

Details

Language :
English
ISSN :
1699-5848
Volume :
23
Issue :
8
Database :
MEDLINE
Journal :
Histology and histopathology
Publication Type :
Academic Journal
Accession number :
18498067
Full Text :
https://doi.org/10.14670/HH-23.925