Evidence map›Paper›PMID 37730805›Full record

ArticleBone research2023

Osteomodulin downregulation is associated with osteoarthritis development.

Jérémie Zappia, Qiao Tong, Renée Van der Cruyssen, Frederique M F Cornelis, Cécile Lambert, Tiago Pinto Coelho, Juliane Grisart, Erika Kague, Rik J Lories, Marc Muller and 4 more

Open access · goldAbstract read
In one paragraph

Article in Bone research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

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  11. Osteomodulin deficiency in mice causes a specific reduction of transversal cortical bone size.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Article
  12. Review
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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

14 authors at 4 institutions in 2 countries.

Jérémie ZappiaMusculoSKeletal Innovative Research Lab, Center for Interdisciplinary Research on Medicines, Université de Liège, Liège, Belgium. jzappia@uliege.be.
Qiao TongSchool of Physiology, Pharmacology, and Neuroscience, University of Bristol, Bristol, UK.
Renée Van der CruyssenDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Frederique M F CornelisLaboratory of Tissue Homeostasis and Disease, Skeletal Biology and Engineering Research Center, Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
Cécile LambertMusculoSKeletal Innovative Research Lab, Center for Interdisciplinary Research on Medicines, Université de Liège, Liège, Belgium.
Tiago Pinto CoelhoCardiovascular Sciences, Groupe Interdisciplinaire de Génoprotéomique Appliquée, Université de Liège, Liège, Belgium.
Juliane GrisartArtialis SA, Tour GIGA, CHU Sart-Tilman, Liège, Belgium.
Erika KagueSchool of Physiology, Pharmacology, and Neuroscience, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0002-0266-9424
Rik J LoriesLaboratory of Tissue Homeostasis and Disease, Skeletal Biology and Engineering Research Center, Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
Marc MullerLaboratoire d'Organogenèse et Régénération, Groupe Interdisciplinaire de Génoprotéomique Appliquée, Université de Liège, Liège, Belgium.ORCID http://orcid.org/0000-0001-6030-2164
Dirk ElewautDepartment of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Chrissy L HammondSchool of Physiology, Pharmacology, and Neuroscience, University of Bristol, Bristol, UK.
Christelle SanchezMusculoSKeletal Innovative Research Lab, Center for Interdisciplinary Research on Medicines, Université de Liège, Liège, Belgium.
Yves HenrotinMusculoSKeletal Innovative Research Lab, Center for Interdisciplinary Research on Medicines, Université de Liège, Liège, Belgium.
University of Liège · BEUniversity of Bristol · GBGhent University Hospital · BEKU Leuven · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abnormal subchondral bone remodeling leading to sclerosis is a main feature of osteoarthritis (OA), and osteomodulin (OMD), a proteoglycan involved in extracellular matrix mineralization, is associated with the sclerotic phenotype. However, the functions of OMD remain poorly understood, specifically in vivo. We used Omd knockout and overexpressing male mice and mutant zebrafish to study its roles in bone and cartilage metabolism and in the development of OA. The expression of Omd is deeply correlated with bone and cartilage microarchitectures affecting the bone volume and the onset of subchondral bone sclerosis and spontaneous cartilage lesions. Mechanistically, OMD binds to RANKL and inhibits osteoclastogenesis, thus controlling the balance of bone remodeling. In conclusion, OMD is a key factor in subchondral bone sclerosis associated with OA. It participates in bone and cartilage homeostasis by acting on the regulation of osteoclastogenesis. Targeting OMD may be a promising new and personalized approach for OA.

Indexed as

OsteoarthritisZebrafishAnimalsDown-RegulationExtracellular Matrix ProteinsMaleMiceProteoglycansSclerosisExtracellular Matrix ProteinsosteoadherinProteoglycans

Identifiers

PMID37730805
PMCPMC10511717
OpenAlexW4386896825

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.