Quantitative histomorphometric analysis of halved iliac crest bone biopsies yield comparable ROD diagnosis as full 7.5mm wide samples.


Journal

Bone
ISSN: 1873-2763
Titre abrégé: Bone
Pays: United States
ID NLM: 8504048

Informations de publication

Date de publication:
09 2020
Historique:
received: 26 01 2020
revised: 27 05 2020
accepted: 27 05 2020
pubmed: 3 6 2020
medline: 22 6 2021
entrez: 3 6 2020
Statut: ppublish

Résumé

Histomorphometric analysis of a transiliac bone biopsy is the gold standard for the diagnosis of renal osteodystrophy (ROD). This procedure is costly, invasive and usually performed with a trephine with an internal diameter of 7.5 mm. Our objective was to evaluate the accuracy of ROD diagnosis on halved histological bone sections to determine if they are comparable to the standard 7.5 mm samples. We included 68 bone biopsies performed in CKD patients for diagnostic purposes with a 7.5 mm diameter trephine. Quantitative histomorphometric analysis of the whole bone samples was performed including assessment of bone mineralization, turnover and volume. Each histological section (representing the whole 7.5 mm diameter biopsy) was then divided lengthwise in two hemisections (representing the 3.5 mm diameter biopsy). Histomorphometric analysis was repeated this time on the two hemibiopsies for each sample, blinded from initial results. Diagnoses were classified as osteitis fibrosa, adynamic bone disease, mixed uremic bone disease, osteomalacia or other. Correlations between the whole sample and the hemibiopsies for each parameter were studied. Concordance between the various bone parameters and final ROD diagnosis obtained from the whole section versus the two hemi sections was evaluated. Highly significant correlations were found between parameters measured on the whole section and the corresponding hemisections, with r coefficient of 0.98 for osteoid surface and thickness and bone formation rate, 0.97 for osteoclast surface, and 0.96 for bone volume (p < 0.001). Final diagnosis was in full accordance between the whole biopsy and the two corresponding hemi-biopsies in 91% of cases. Accurate diagnosis of ROD type was obtained by evaluation of bone surface areas of 3 mm diameter. These data suggest that small invasive bone biopsies might provide accurate ROD diagnostics while decreasing both invasiveness and cost of the procedure.

Sections du résumé

BACKGROUND AND OBJECTIVES
Histomorphometric analysis of a transiliac bone biopsy is the gold standard for the diagnosis of renal osteodystrophy (ROD). This procedure is costly, invasive and usually performed with a trephine with an internal diameter of 7.5 mm. Our objective was to evaluate the accuracy of ROD diagnosis on halved histological bone sections to determine if they are comparable to the standard 7.5 mm samples.
DESIGN
We included 68 bone biopsies performed in CKD patients for diagnostic purposes with a 7.5 mm diameter trephine. Quantitative histomorphometric analysis of the whole bone samples was performed including assessment of bone mineralization, turnover and volume. Each histological section (representing the whole 7.5 mm diameter biopsy) was then divided lengthwise in two hemisections (representing the 3.5 mm diameter biopsy). Histomorphometric analysis was repeated this time on the two hemibiopsies for each sample, blinded from initial results. Diagnoses were classified as osteitis fibrosa, adynamic bone disease, mixed uremic bone disease, osteomalacia or other. Correlations between the whole sample and the hemibiopsies for each parameter were studied. Concordance between the various bone parameters and final ROD diagnosis obtained from the whole section versus the two hemi sections was evaluated.
RESULTS
Highly significant correlations were found between parameters measured on the whole section and the corresponding hemisections, with r coefficient of 0.98 for osteoid surface and thickness and bone formation rate, 0.97 for osteoclast surface, and 0.96 for bone volume (p < 0.001). Final diagnosis was in full accordance between the whole biopsy and the two corresponding hemi-biopsies in 91% of cases.
CONCLUSIONS
Accurate diagnosis of ROD type was obtained by evaluation of bone surface areas of 3 mm diameter. These data suggest that small invasive bone biopsies might provide accurate ROD diagnostics while decreasing both invasiveness and cost of the procedure.

Identifiants

pubmed: 32485361
pii: S8756-3282(20)30240-4
doi: 10.1016/j.bone.2020.115460
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

115460

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Etienne Novel-Catin (E)

INSERM U1059 and University Hospital, Saint-Etienne, France; Université de Lyon, Lyon, France; Department of Nephrology, University Hospital - Lyon Sud, France. Electronic address: etienne.novel-catin@chu-lyon.fr.

Solenne Pelletier (S)

Department of Nephrology, University Hospital - Lyon Sud, France. Electronic address: solenne.pelletier@chu-lyon.fr.

Denis Fouque (D)

Université de Lyon, Lyon, France; Department of Nephrology, University Hospital - Lyon Sud, France. Electronic address: denis.fouque@chu-lyon.fr.

Jean-Paul Roux (JP)

Université de Lyon, Lyon, France; INSERM UMR 1033, Lyon Cedex 08, France. Electronic address: jean-paul.roux@univ-lyon1.fr.

Roland Chapurlat (R)

Université de Lyon, Lyon, France; INSERM UMR 1033, Lyon Cedex 08, France. Electronic address: roland.chapurlat@chu-lyon.fr.

Patrick D'Haese (P)

Laboratory of Pathophysiology, University of Antwerp, Wilrijk, Belgium. Electronic address: patrick.dhaese@uantwerpen.be.

Geert Behets (G)

Laboratory of Pathophysiology, University of Antwerp, Wilrijk, Belgium. Electronic address: Geert.Behets@uantwerpen.be.

Peter Evenepoel (P)

KU Leuven, Department of Microbiology and Immunology, Laboratory of Nephrology, Belgium. Electronic address: pieter.evenepoel@uzleuven.be.

Thomas L Nickolas (TL)

Columbia University Medical Center, New York, NY, United States. Electronic address: tln2001@cumc.columbia.edu.

Marie-Hélène Lafage-Proust (MH)

INSERM U1059 and University Hospital, Saint-Etienne, France; Université de Lyon, Lyon, France. Electronic address: mh.lafage.proust@univ-st-etienne.fr.

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