Evidence map›Paper›PMID 39521711›Full record

ArticleAnais brasileiros de dermatologia

Red light-emitting diode on skin healing: an in vitro and in vivo experimental study.

Tuany R Schmidt, Belkiss C Mármora, Fernanda T Brochado, Lucas Gonçalves, Paloma S Campos, Marcelo L Lamers, Aurigena A de Araújo, Caroline A C X de Medeiros, Susana B Ribeiro, Marco A T Martins and 3 more

Abstract read
In one paragraph

Article in Anais brasileiros de dermatologia. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

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

13 authors.

Tuany R SchmidtDepartment of Pathology, Faculty of Dentistry, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Belkiss C MármoraDepartment of Pathology, Faculty of Dentistry, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Fernanda T BrochadoDepartment of Pathology, Faculty of Dentistry, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Lucas GonçalvesDepartment of Pathology, Faculty of Dentistry, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil; Department of Pediatric Dentistry, Orthodontics and Public Health, Faculty of Dentistry, Universidade de São Paulo, Bauru, SP, Brazil.
Paloma S CamposDepartment of Pathology, Faculty of Dentistry, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Marcelo L LamersDepartment of Pathology, Faculty of Dentistry, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Aurigena A de AraújoPost-Graduation Program Oral Science/Post-Graduation Program in Pharmaceutical Science, Department of Biophysics and Pharmacology, Universidade Federal do Rio Grande do Norte, Natal, RN, Brazil.
Caroline A C X de MedeirosDepartment of Biophysics and Pharmacology/ Postgraduate Program in Biological Science and Rede Nordeste de Biotecnologia, Universidade Federal do Rio Grande Norte, Natal, RN, Brazil.
Susana B RibeiroPostgraduate Program in Biological Science and Rede Nordeste de Biotecnologia/Renorbio, Universidade Federal do Rio Grande Norte, Natal, RN, Brazil.
Marco A T MartinsDepartment of Pathology, Faculty of Dentistry, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil; Department of Oral Medicine, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Emily F S PilarExperimental Pathology Unit, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Manoela D MartinsDepartment of Pathology, Faculty of Dentistry, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil; Department of Oral Medicine, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil; Department of Oral Diagnosis, Faculty of Dentistry, Universidade de Campinas, Piracicaba, SP, Brazil.
Vivian P WagnerDepartment of Oral Diagnosis, Faculty of Dentistry, Universidade de Campinas, Piracicaba, SP, Brazil; Oral Medicine Department, Faculty of Dentistry, Universidade de São Paulo São Paulo, SP, Brazil. Electronic address: vivianpwagner@usp.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe clinical advantages of light-emitting diode (LED) therapy in skin healing and its underlying mechanism remain subjects of ongoing debate.

objectiveThis study aims to explore the impact of LED therapy on normal skin keratinocytes (HaCaT) and in the repair of full-thickness dorsal wounds in Wistar rats.

methodsHaCaT cell viability (SRB assay) and migration (scratch assay) were assessed under LED therapy, comparing stress conditions (2.5% FBS) with sham irradiation and optimal conditions (10% FBS). In vivo, 50 rats with induced wounds were divided into Sham and LED (daily treatment) groups. Euthanasia occurred at 3, 5, 10, 14, and 21 days for clinical, morphological, oxidative stress (MDA, SOD, and GSH), and cytokine analyses (IL-1β, IL-10, TNF-α).

resultsLED therapy significantly enhanced keratinocytes viability compared to sham irradiation, with minimal impact on cell migration. Clinical benefits were prominent on day 10, influencing inflammation progression and resolution on days 3 and 10. Re-epithelization remained unaffected. Reduced MDA and increased GSH levels were observed throughout, while SOD levels varied temporally. Notably, on day 10, LED significantly decreased IL-1β, IL-10, and TNF-α. STUDY LIMITATIONS: Although translational, clinical trial confirmation of observed benefits is warranted.

conclusionsLED therapy expedites cutaneous healing in the experimental model, primarily modulating inflammation and enhancing antioxidant activity.

Indexed as

Cell SurvivalKeratinocytesOxidative StressPhototherapyRats, WistarWound HealingAnimalsCell MovementCytokinesHumansMaleRatsRed LightSkinTime FactorsCytokinesCell culture techniquesCytokinesDermatologyLow-level light therapyModels, animalOxidative stress

Identifiers

PMID39521711
PMCPMC11745292

What OpenQuestion holds

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LicenceCC BY
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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.