Evidence map›Paper›PMID 21395504›Full record

ReviewCritical reviews in eukaryotic gene expression2010

Heterotopic ossification has some nerve.

Elizabeth Salisbury, Corinne Sonnet, Michael Heggeness, Alan R Davis, Elizabeth Olmsted-Davis

Abstract readReview
In one paragraph

Review in Critical reviews in eukaryotic gene expression, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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  5. Review
  6. A microCT-based platform to quantify drug targeting.European radiology experimental · 2023
    Article
  7. Article
  8. Review
  9. Article
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  11. Review
  12. Review
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  14. Crosstalk between substance P and calcitonin gene-related peptide during heterotopic ossification in murine Achilles tendon.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2018
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Location-dependent heterotopic ossification in the rat model: The role of activated matrix metalloproteinase 9.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2016
    Article
  20. 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

5 authors at 2 institutions in 2 countries.

Elizabeth SalisburyCenter for Cell and Gene Therapy; and Translational Biology and Molecular Medicine, Baylor College of Medicine, Houston, TX 77030, USA.
Corinne Sonnet
Michael Heggeness
Alan R Davis
Elizabeth Olmsted-Davis
Baylor College of Medicine · USCenter for Translational Molecular Medicine · NL

Funding

Training In Cell and Gene TherapyT32HL092332 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI MALCOLM K. BRENNER, Bruno Di Stefano · 2008 to 2026
$6.9M
Tissue Engineering of Hematopoietic BoneR01EB005173 · NIBIB · BAYLOR COLLEGE OF MEDICINE · PI HIRSCHI, KAREN KEMPER · 2005 to 2009
$5.9M
Human Endothelial Cell DifferentiationR01HL096360 · NHLBI · YALE UNIVERSITY · PI HIRSCHI, KAREN KEMPER · 2009 to 2013
$1.5M
NHLBI NIH HHS R01 HL096360NHLBI NIH HHS T32 HL092332NHLBI NIH HHS T-32 HL092332-08NIBIB NIH HHS R01 EB005173NIBIB NIH HHS R01EB005173-01
6 · The paper itself

Abstract

Heterotopic ossification, defined as the formation of bone in abnormal anatomic locations, can be clinically insignificant or devastating and debilitating, depending on the site and duration of new bone formation. There are many causes of heterotopic ossification (HO), including soft tissue trauma, central nervous system injury, vasculopathies, arthropathies, and inheritance. One of the least understood components of HO is the interaction of the peripheral nervous system with the induction of this process. Recent work has shown that, upon traumatic injury, a cascade of events termed neurogenic inflammation is initiated, which involves the release of neuropeptides, such as substance P and calcitonin gene related peptide. Release of these peptides ultimately leads to the recruitment of activated platelets, mast cells, and neutrophils to the injury site. These cells appear to be involved with both remodeling of the nerve, as well as potentially recruiting additional cells from the bone marrow to the injury site. Further, sensory neurons stimulated at the injury site relay local information to the brain, which can then redirect neuroendocrine signaling in the hypothalamus towards repair of the injured site. While numerous studies have highlighted the important role of nerve-derived signals, both central and peripheral, in the regulation of normal bone remodeling of the skeleton,1 this review focuses on the role of the local, peripheral nerves in the formation of heterotopic bone. We concentrate on the manner in which local changes in bone morphogenetic protein (BMP) expression contribute to a cascade of events within the peripheral nerves, both sensory and sympathetic, in the immediate area of HO formation.

Indexed as

AnimalsBone Morphogenetic ProteinsHumansInflammationMiceModels, NeurologicalNeuropeptidesOssification, HeterotopicOsteoblastsPeripheral Nervous SystemSignal TransductionTRPV Cation ChannelsBone Morphogenetic ProteinsNeuropeptidesTRPV1 protein, mouseTRPV Cation Channels

Identifiers

PMID21395504
PMCPMC4535924
OpenAlexW1966513399

What OpenQuestion holds

Textmetadata
LicenceTDM
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.