Evidence mapPaperPMID 40367355Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2025

Pain in fibrous dysplasia: identifying nociceptive mechanisms in a preclinical model.

Chelsea Hopkins, Luis Fernandez de Castro, Julie Benthin, Marta Diaz-delCastillo, Pravallika Manjappa, Alison Boyce, Ruth Elena Martinez Mendoza, Juan Antonio Vazquez Mora, Giovanni Emmanuel Lopez-Delgado, Lizeth Yazmin Ponce Gomez and 5 more

Abstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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

15 authors.

Chelsea HopkinsDepartment of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, 2100, Denmark.ORCID 0000-0003-1320-7644
Luis Fernandez de CastroSkeletal Disorders and Mineral Homeostasis Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, 9000, MD, United States.ORCID 0000-0003-3194-9780
Julie BenthinDepartment of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, 2100, Denmark.
Marta Diaz-delCastilloDepartment of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, 2100, Denmark.ORCID 0000-0001-7719-6839
Pravallika ManjappaNeuroscience, Biopharmaceuticals R&D, AstraZeneca, Cambridge, CB2 0AA, United Kingdom.
Alison BoyceMetabolic Bone Disorders Unit, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, 9000, MD, United States.ORCID 0000-0003-2987-3887
Ruth Elena Martinez MendozaDepartment of Unidad Académica Multidisciplinaria Reynosa, Aztlán Universidad Autónoma de Tamaulipas Reynosa, Tamaulipas, 88740, Mexico.
Juan Antonio Vazquez MoraDepartment of Unidad Académica Multidisciplinaria Reynosa, Aztlán Universidad Autónoma de Tamaulipas Reynosa, Tamaulipas, 88740, Mexico.ORCID 0000-0002-2836-7424
Giovanni Emmanuel Lopez-DelgadoDepartment of Unidad Académica Multidisciplinaria Reynosa, Aztlán Universidad Autónoma de Tamaulipas Reynosa, Tamaulipas, 88740, Mexico.
Lizeth Yazmin Ponce GomezDepartment of Unidad Académica Multidisciplinaria Reynosa, Aztlán Universidad Autónoma de Tamaulipas Reynosa, Tamaulipas, 88740, Mexico.
Khaled Elhady MohamedDepartment of Endocrinology, Nordic Bioscience, Herlev, 2730, Denmark.
John E LinleyNeuroscience, Biopharmaceuticals R&D, AstraZeneca, Cambridge, CB2 0AA, United Kingdom.
Michael T CollinsSkeletal Disorders and Mineral Homeostasis Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, 9000, MD, United States.
Juan Miguel Jimenez-AndradeDepartment of Unidad Académica Multidisciplinaria Reynosa, Aztlán Universidad Autónoma de Tamaulipas Reynosa, Tamaulipas, 88740, Mexico.
Anne-Marie HeegaardDepartment of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, 2100, Denmark.ORCID 0000-0003-2754-0800

Funding

European Union's Horizon 2020 814244
6 · The paper itself

Abstract

Pain is a common symptom of fibrous dysplasia (FD), a rare mosaic disorder characterized by fibro-osseous lesions in the bone. Despite the prevalence of pain in FD patients, there is little knowledge about the nociceptive mechanisms and few efficacious treatments. As such, understanding FD pain is essential for patient care. The overall aim of this study was to identify nocifensive behaviors and potential underlying mechanisms in a transgenic mouse model of FD, previously shown to display high face and translational validity. Significant nocifensive behaviors were observed in FD mice (male and female), compared to control mice in the burrowing, grid hanging, home cage activity, and wheel running assays. These changes corresponded to lesion development, as visualized by X-ray imaging. Behavioral deficits improved when analgesics were administered, indicating a nociceptive origin. Tibias and femurs from FD mice demonstrated characteristic FD lesions and the presence of mono- and multi-nucleated CD68+ cells, calcitonin gene-related peptide sensory nerve fibers, and vascularization. Lumbar dorsal root ganglia from male FD mice displayed increased staining for activating transcription factor-3 and tyrosine hydroxylase neurons. No difference was observed in the spinal cords between the FD and control groups for glial cell presence and neuropeptide expression. Bone marrow stromal cells were obtained from FD and control mice and cultured in vitro. FD cells developed an increased concentration of inflammatory cytokines (IL-6, tumor necrosis factor-alpha), chemokines (monocyte chemoattractant protein, keratinocyte chemoattractant/human growth-regulated oncogene), and nerve growth factor as compared to controls. Taken together, this study demonstrated for the first time that nociceptive mechanisms such as axonal growth in FD lesions, nerve injury, and inflammation may contribute to FD pain, and it provides a foundation for conducting further studies of pain- and disease-modifying therapeutics for FD patients.

Indexed as

Fibrous Dysplasia of BoneNociceptionPainAnimalsDisease Models, AnimalFemaleGanglia, SpinalHumansMaleMiceMice, Transgenicbone painfibrous dysplasiain vivomechanismpain

Identifiers

PMID40367355
PMCPMC12188752

What Socratic 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 Socratic graph.