Evidence map›Paper›PMID 24586331›Full record

ArticlePloS one2014

Alterations of mass density and 3D osteocyte lacunar properties in bisphosphonate-related osteonecrotic human jaw bone, a synchrotron µCT study.

Bernhard Hesse, Max Langer, Peter Varga, Alexandra Pacureanu, Pei Dong, Susanne Schrof, Nils Männicke, Heikki Suhonen, Cecile Olivier, Peter Maurer and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 52 citations in OpenAlex.

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  19. 3D X-ray ultra-microscopy of bone tissue.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2016
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 4 countries.

Bernhard HesseEuropean Synchrotron Radiation Facility, Grenoble, France ; Berlin-Brandenburg School for Regenerative Therapies & Julius Wolff Institut, Charité, Universitätsmedizin Berlin, Germany.
Max LangerEuropean Synchrotron Radiation Facility, Grenoble, France ; Université de Lyon, CREATIS, CNRS UMR5220, INSA-Lyon, Lyon, France.
Peter VargaBerlin-Brandenburg School for Regenerative Therapies & Julius Wolff Institut, Charité, Universitätsmedizin Berlin, Germany.
Alexandra PacureanuEuropean Synchrotron Radiation Facility, Grenoble, France ; Université de Lyon, CREATIS, CNRS UMR5220, INSA-Lyon, Lyon, France ; Centre for Image Analysis and Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Pei DongEuropean Synchrotron Radiation Facility, Grenoble, France ; Université de Lyon, CREATIS, CNRS UMR5220, INSA-Lyon, Lyon, France.
Susanne SchrofBerlin-Brandenburg School for Regenerative Therapies & Julius Wolff Institut, Charité, Universitätsmedizin Berlin, Germany.
Nils MännickeBerlin-Brandenburg School for Regenerative Therapies & Julius Wolff Institut, Charité, Universitätsmedizin Berlin, Germany.
Heikki SuhonenEuropean Synchrotron Radiation Facility, Grenoble, France.
Cecile OlivierEuropean Synchrotron Radiation Facility, Grenoble, France ; Université de Lyon, CREATIS, CNRS UMR5220, INSA-Lyon, Lyon, France.
Peter MaurerKlinik für Mund-, Kiefer- und Gesichtschirurgie, Klinikum Bremerhaven-Reinkenheide, Kiel, Germany.
Galateia J KazakiaDepartment of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, California, United States of America.
Kay RaumBerlin-Brandenburg School for Regenerative Therapies & Julius Wolff Institut, Charité, Universitätsmedizin Berlin, Germany.
Francoise PeyrinEuropean Synchrotron Radiation Facility, Grenoble, France ; Université de Lyon, CREATIS, CNRS UMR5220, INSA-Lyon, Lyon, France.
European Synchrotron Radiation Facility · FRBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DEKlinikum Bremerhaven-Reinkenheide · DEScience for Life Laboratory · SEUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteonecrosis of the jaw, in association with bisphosphonates (BRONJ) used for treating osteoporosis or cancer, is a severe and most often irreversible side effect whose underlying pathophysiological mechanisms remain largely unknown. Osteocytes are involved in bone remodeling and mineralization where they orchestrate the delicate equilibrium between osteoclast and osteoblast activity and through the active process called osteocytic osteolysis. Here, we hypothesized that (i) changes of the mineralized tissue matrix play a substantial role in the pathogenesis of BRONJ, and (ii) the osteocyte lacunar morphology is altered in BRONJ. Synchrotron µCT with phase contrast is an appropriate tool for assessing both the 3D morphology of the osteocyte lacunae and the bone matrix mass density. Here, we used this technique to investigate the mass density distribution and 3D osteocyte lacunar properties at the sub-micrometer scale in human bone samples from the jaw, femur and tibia. First, we compared healthy human jaw bone to human tibia and femur in order to assess the specific differences and address potential explanations of why the jaw bone is exclusively targeted by the necrosis as a side effect of BP treatment. Second, we investigated the differences between BRONJ and control jaw bone samples to detect potential differences which could aid an improved understanding of the course of BRONJ. We found that the apparent mass density of jaw bone was significantly smaller compared to that of tibia, consistent with a higher bone turnover in the jaw bone. The variance of the lacunar volume distribution was significantly different depending on the anatomical site. The comparison between BRONJ and control jaw specimens revealed no significant increase in mineralization after BP. We found a significant decrease in osteocyte-lacunar density in the BRONJ group compared to the control jaw. Interestingly, the osteocyte-lacunar volume distribution was not altered after BP treatment.

Indexed as

Analysis of VarianceBisphosphonate-Associated Osteonecrosis of the JawBone DensityHumansImage Processing, Computer-AssistedOsteocytesSynchrotronsX-Ray Microtomography

Identifiers

PMID24586331
PMCPMC3931622
OpenAlexW2010214138

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.