Evidence map›Paper›PMID 32303916›Full record

ArticleJournal of bone and mineral metabolism2020

Marine collagen scaffolds and photobiomodulation on bone healing process in a model of calvaria defects.

M A Cruz, K R Fernandes, J R Parisi, G C A Vale, S R A Junior, F R Freitas, A F S Sales, C A Fortulan, O Peitl, E Zanotto and 3 more

Abstract read
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In one paragraph

Article in Journal of bone and mineral metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

M A CruzDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Santos, Brazil. allmayda07@gmail.com.ORCID http://orcid.org/0000-0002-9032-9111
K R FernandesDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Santos, Brazil.
J R ParisiDepartment of Fisiotherapy, Federal University of São Carlos (UFSCar), São Carlos, Brazil.
G C A ValeDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Santos, Brazil.
S R A JuniorDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Santos, Brazil.
F R FreitasDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Santos, Brazil.
A F S SalesDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Santos, Brazil.
C A FortulanDepartment of Fisiotherapy, Federal University of São Carlos (UFSCar), São Carlos, Brazil.
O PeitlDepartment of Fisiotherapy, Federal University of São Carlos (UFSCar), São Carlos, Brazil.
E ZanottoDepartment of Fisiotherapy, Federal University of São Carlos (UFSCar), São Carlos, Brazil.
R N GranitoDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Santos, Brazil.
A M RibeiroDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Santos, Brazil.
A C M RennoDepartment of Biosciences, Federal University of São Paulo (UNIFESP), Santos, Brazil.
Universidade Federal de São Paulo · BRUniversidade Federal de São Carlos · BR

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 001Fundação de Amparo à Pesquisa do Estado de São Paulo 2016/13636-9
6 · The paper itself

Abstract

introductionCollagen from marine esponges has been used as a promising material for tissue engineering proposals. Similarly, photobiomodulation (PBM) is able of modulating inflammatory processes after an injury, accelerating soft and hard tissue healing and stimulating neoangiogenesis. However, the effects of the associated treatments on bone tissue healing have not been studied yet. In this context, the present study aimed to evaluate the biological temporal modifications (using two experimental periods) of marine sponge collagen or sponging (SPG) based scaffold and PBM on newly formed bone using a calvaria bone defect model. MATERIAL AND

methodsWistar rats were distributed into two groups: SPG or SPG/PBM and euthanized into two different experimental periods (15 and 45 days post-surgery). A cranial critical bone defect was used to evaluate the effects of the treatments. Histology, histomorfometry and immunohistological analysis were performed.

resultsHistological findings demonstrated that SPG/PBM-treated animals, 45 days post-surgery, demonstrated a higher amount of connective and newly formed bone tissue at the region of the defect compared to CG. Notwithstanding, no difference among groups were observed in the histomorphometry. Interestingly, for both anti-transforming growth factor-beta (TGF-β) and anti-vascular endothelial growth factor (VEGF) immunostaining, higher values for SPG/PBM, at 45 days post-surgery could be observed.

conclusionIt can be concluded that the associated treatment can be considered as a promising therapeutical intervention.

Indexed as

Low-Level Light TherapyAnimalsAquatic OrganismsCollagenDisease Models, AnimalMaleRats, WistarSkullTissue ScaffoldsTransforming Growth Factor betaVascular Endothelial Growth Factor AWound HealingCollagenTransforming Growth Factor betaVascular Endothelial Growth Factor ABiomaterialsBone healingCollagenHistomorphometryMarine spongesPhotobiomodulation

Identifiers

PMID32303916
OpenAlexW3016610163

What OpenQuestion holds

Textmetadata
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.