Evidence map›Paper›PMID 30463618›Full record

ArticleJournal of translational medicine2018

Optimizing bone wound healing using BMP2 with absorbable collagen sponge and Talymed nanofiber scaffold.

Emily L Durham, R Nicole Howie, SarahRose Hall, Nicholas Larson, Brayden Oakes, Reed Houck, Zachary Grey, Martin Steed, Amanda C LaRue, Robin Muise-Helmericks and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  15. Engineered Collagen Matrices.Bioengineering (Basel, Switzerland) · 2020
    Review
  16. Article
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  18. Article
  19. Sub-clinical dose of bone morphogenetic protein-2 does not precipitate rampant, sustained inflammatory response in bone wound healing.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society · 2019
    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

11 authors at 3 institutions in 1 country.

Emily L DurhamDepartment of Oral Health Sciences, Medical University of South Carolina, 173 Ashley Ave., Charleston, SC, 29425, USA.
R Nicole HowieDepartment of Oral Health Sciences, Medical University of South Carolina, 173 Ashley Ave., Charleston, SC, 29425, USA.
SarahRose HallDepartment of Oral Health Sciences, Medical University of South Carolina, 173 Ashley Ave., Charleston, SC, 29425, USA.
Nicholas LarsonDepartment of Oral Health Sciences, Medical University of South Carolina, 173 Ashley Ave., Charleston, SC, 29425, USA.
Brayden OakesCollege of Dental Medicine, Medical University of South Carolina, 173 Ashley Ave., Charleston, SC, 29425, USA.
Reed HouckCollege of Dental Medicine, Medical University of South Carolina, 173 Ashley Ave., Charleston, SC, 29425, USA.
Zachary GreyDepartment of Oral Health Sciences, Medical University of South Carolina, 173 Ashley Ave., Charleston, SC, 29425, USA.
Martin SteedDepartment of Oral and Maxillofacial Surgery, Medical University of South, 173 Ashley Ave., Charleston, SC, 29425, USA.
Amanda C LaRueDepartment of Pathology and Laboratory Medicine, Medical University of South, 173 Ashley Ave., Charleston, SC, 29425, USA.
Robin Muise-HelmericksDepartment of Regenerative Medicine, Medical University of South Carolina, 173 Ashley Ave., Charleston, SC, 29425, USA.
James CrayDivision of Anatomy, Department of Biomedical Education & Anatomy, The Ohio State University College of Medicine, 279 Hamilton Hall, 1645 Neil Ave., Columbus, OH, 43210, USA. James.Cray@osumc.edu.
Medical University of South Carolina · USRalph H. Johnson VA Medical Center · USThe Ohio State University · US

Funding

T-COHR: Training in Craniofacial and Oral Health ResearchT32DE017551 · NIDCR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YAO, HAI · 2006 to 2025
$10.3M
The effects of pharmacological exposures on cranial suture stem cellsF31DE026684 · NIDCR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI DURHAM, EMILY LENSIE · 2017 to 2018
$90k
Potential of Hematopoietic Stem Cell-Based Therapies for Complicated FracturesI01BX000333 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI LARUE, AMANDA C. · 2009 to 2022
–
AO Foundation S-16-108CBLRD VA I01 BX000333Marine Polymer Technologies Product in KindMedtronic Product in KindNIDCR NIH HHS 5T32DE017551]NIDCR NIH HHS F31 DE026684NIDCR NIH HHS F31DE026684NIDCR NIH HHS T32 DE017551NIGMS NIH HHS P30GM10331
6 · The paper itself

Abstract

backgroundBone is a highly vascularized and resilient organ with innate healing abilities, however some bone injuries overwhelm these attributes and require intervention, such as bone tissue engineering strategies. Combining biomaterials and growth factors, such as bone morphogenetic protein 2 (BMP2), is one of the most commonly used tissue engineering strategies. However, use of BMP2 has been correlated with negative clinical outcomes including aberrant inflammatory response, poor quality bone, and ectopic bone.

methodsIn the present study, a novel poly-n-acetyl glucosamine (pGlcNAc, trade name Talymed) scaffold was utilized in addition to the commonly used acellular collagen sponge (ACS) BMP2 delivery system in a murine calvarial defect model to investigate whether the innate properties of Talymed can reduce the noted negative bone phenotypes associated with BMP2 treatment.

resultsComparison of murine calvarial defect healing between ACS with and without Talymed revealed that there was no measurable healing benefit for the combined treatment. Healing was most effective utilizing the traditional acellular collagen sponge with a reduced dose of BMP2.

conclusionsThe results of this investigation lead to the conclusion that excessive dosing of BMP2 may be responsible for the negative clinical side effects observed with this bone tissue engineering strategy. Rather than augmenting the currently used ACS BMP2 bone wound healing strategy with an additional anti-inflammatory scaffold, reducing the dose of BMP2 used in the traditional delivery system results in optimal healing without the published negative side effects of BMP2 treatment.

Indexed as

AnimalsBone Morphogenetic Protein 2CollagenFemaleMaleMice, Inbred C57BLNanofibersSkullTissue ScaffoldsWound HealingX-Ray MicrotomographyBone Morphogenetic Protein 2CollagenBiomaterialsBMP2Bone wound healing

Identifiers

PMID30463618
PMCPMC6249740
OpenAlexW2901070172

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.