Evidence map›Paper›PMID 24801669›Full record

ArticleHead & neck2015

Targeting angiogenesis as a therapeutic means to reinforce osteocyte survival and prevent nonunions in the aftermath of radiotherapy.

Alexis Donneys, Noah S Nelson, Erin E Page, Sagar S Deshpande, Peter A Felice, Catherine N Tchanque-Fossuo, Joshua P Spiegel, Steven R Buchman

Open access · greenAbstract readComparative Study
In one paragraph

Article in Head & neck, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
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  3. Review
  4. Article
  5. Article
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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

8 authors at 2 institutions in 1 country.

Alexis DonneysCraniofacial Research Laboratory, Plastic Surgery Section, University of Michigan, Ann Arbor, Michigan.
Noah S NelsonCraniofacial Research Laboratory, Plastic Surgery Section, University of Michigan, Ann Arbor, Michigan.
Erin E PageCraniofacial Research Laboratory, Plastic Surgery Section, University of Michigan, Ann Arbor, Michigan.
Sagar S DeshpandeCraniofacial Research Laboratory, Plastic Surgery Section, University of Michigan, Ann Arbor, Michigan.
Peter A FeliceCraniofacial Research Laboratory, Plastic Surgery Section, University of Michigan, Ann Arbor, Michigan.
Catherine N Tchanque-FossuoCraniofacial Research Laboratory, Plastic Surgery Section, University of Michigan, Ann Arbor, Michigan.
Joshua P SpiegelCraniofacial Research Laboratory, Plastic Surgery Section, University of Michigan, Ann Arbor, Michigan.
Steven R BuchmanCraniofacial Research Laboratory, Plastic Surgery Section, University of Michigan, Ann Arbor, Michigan.
University of Michigan–Ann Arbor · USUniversity of South Carolina · US

Funding

TRAINING GRANT IN TRAUMA, BURN AND WOUND HEALING RESEARCT32GM008616 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BUCHMAN, STEVEN R, CHUNG, KEVIN C · 1997 to 2025
$3.1M
Translational Optimization of Bone Regeneration in the Irradiated MandibleR01CA125187 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BUCHMAN, STEVEN R · 2007 to 2017
$2.8M
NCI NIH HHS CA12587-06NCI NIH HHS R01 CA125187NIGMS NIH HHS T32 GM008616NIGMS NIH HHS T32-GM008616NIMHD NIH HHS L32 MD009814
6 · The paper itself

Abstract

backgroundRadiotherapy (XRT) exerts detrimental collateral effects on bone tissue through mechanisms of vascular damage and impediments to osteocytes, ultimately predisposing patients to the debilitating problems of late pathologic fractures and nonunions. We posit that angiogenic therapy will reverse these pathologic effects in a rat model of radiated fracture healing.

methodsThree groups of rats underwent mandibular osteotomy. Radiated groups received a fractionated 35-Gy dose before surgery. The deferoxamine (DFO) group received local injections postoperatively. A 40-day healing period was allowed before histology. Analysis of variance (ANOVA; p < .05) was used for group comparisons.

resultsRadiated fractures revealed a significantly decreased osteocyte count and corresponding increase in empty lacunae when compared to nonradiated fractures (p = .001). With the addition of DFO, these differences were not appreciated. Further, a 42% increase in bony unions was observed after DFO therapy.

conclusionTargeting angiogenesis is a useful means for promoting osteocyte survival and preventing bone pathology after XRT.

Indexed as

Analysis of VarianceAnimalsBiopsy, NeedleCells, CulturedCell SurvivalDeferoxamineDisease Models, AnimalDose Fractionation, RadiationFracture HealingFractures, UnunitedImmunohistochemistryInjections, IntralesionalMaleMandibleMandibular OsteotomyNeovascularization, PathologicDeferoxamineangiogenesisdeferoxaminemandiblenonunionradiation

Identifiers

PMID24801669
PMCPMC4788100
OpenAlexW1914163679

What OpenQuestion holds

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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.