Evidence map›Paper›PMID 39527574›Full record

ReviewACS biomaterials science & engineering2024

Treatment of Bone Defects and Nonunion via Novel Delivery Mechanisms, Growth Factors, and Stem Cells: A Review.

Quinn T Ehlen, Joseph P Costello, Nicholas A Mirsky, Blaire V Slavin, Marcelo Parra, Albert Ptashnik, Vasudev Vivekanand Nayak, Paulo G Coelho, Lukasz Witek

Abstract readReview
In one paragraph

Review in ACS biomaterials science & engineering, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. DPHD fromACS omega · 2026
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  3. Review
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  6. Article
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  8. 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

9 authors.

Quinn T EhlenUniversity of Miami Miller School of Medicine, Miami, Florida 33136, United States.
Joseph P CostelloUniversity of Miami Miller School of Medicine, Miami, Florida 33136, United States.
Nicholas A MirskyUniversity of Miami Miller School of Medicine, Miami, Florida 33136, United States.
Blaire V SlavinUniversity of Miami Miller School of Medicine, Miami, Florida 33136, United States.
Marcelo ParraCenter of Excellence in Morphological and Surgical Studies (CEMyQ), Faculty of Medicine, Universidad de La Frontera, Temuco 4811230, Chile.
Albert PtashnikBiomaterials Division, NYU Dentistry, New York, New York 10010, United States.
Vasudev Vivekanand NayakDepartment of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, Florida 33136, United States.ORCID 0000-0003-2739-0339
Paulo G CoelhoDepartment of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, Florida 33136, United States.
Lukasz WitekBiomaterials Division, NYU Dentistry, New York, New York 10010, United States.ORCID 0000-0003-1458-6527

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone nonunion following a fracture represents a significant global healthcare challenge, with an overall incidence ranging between 2 and 10% of all fractures. The management of nonunion is not only financially prohibitive but often necessitates invasive surgical interventions. This comprehensive manuscript aims to provide an extensive review of the published literature involving growth factors, stem cells, and novel delivery mechanisms for the treatment of fracture nonunion. Key growth factors involved in bone healing have been extensively studied, including bone morphogenic protein (BMP), vascular endothelial growth factor (VEGF), and platelet-derived growth factor. This review includes both preclinical and clinical studies that evaluated the role of growth factors in acute and chronic nonunion. Overall, these studies revealed promising bridging and fracture union rates but also elucidated complications such as heterotopic ossification and inferior mechanical properties associated with chronic nonunion. Stem cells, particularly mesenchymal stem cells (MSCs), are an extensively studied topic in the treatment of nonunion. A literature search identified articles that demonstrated improved healing responses, osteogenic capacity, and vascularization of fractures due to the presence of MSCs. Furthermore, this review addresses novel mechanisms and materials being researched to deliver these growth factors and stem cells to nonunion sites, including natural/synthetic polymers and bioceramics. The specific mechanisms explored in this review include BMP-induced osteoblast differentiation, VEGF-mediated angiogenesis, and the role of MSCs in multilineage differentiation and paracrine signaling. While these therapeutic modalities exhibit substantial preclinical promise in treating fracture nonunion, there remains a need for further research, particularly in chronic nonunion and large animal models. This paper seeks to identify such translational hurdles which must be addressed in order to progress the aforementioned treatments from the lab to the clinical setting.

Indexed as

Drug Delivery SystemsFractures, UnunitedIntercellular Signaling Peptides and ProteinsAnimalsFracture HealingHumansMesenchymal Stem CellsMesenchymal Stem Cell TransplantationOsteogenesisIntercellular Signaling Peptides and Proteinsbone regenerationFracture nonuniongrowth factorsstem cells

Identifiers

PMID39527574
PMCPMC11632667

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.