Evidence map›Paper›PMID 37997536›Full record

ArticleClinical and experimental dental research2023

Chronological analysis of periodontal bone loss in experimental periodontitis in mice.

Cristhiam de J Hernández Martínez, Pedro Felix Silva, Sergio L Salvador, Michel Messora, Daniela B Palioto

Open access · goldAbstract read
In one paragraph

Article in Clinical and experimental dental research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. M2 Macrophage-Derived Extracellular Vesicles Reprogram Immature Neutrophils into Anxa1Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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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

5 authors at 2 institutions in 1 country.

Cristhiam de J Hernández MartínezDepartment of Oral & Maxillofacial Surgery and Periodontology, Ribeirão Preto Dental School, University of Sao Paulo-USP, Ribeirão Preto SP, Brazil.ORCID 0000-0002-8053-8366
Pedro Felix SilvaDepartment of Oral & Maxillofacial Surgery and Periodontology, Ribeirão Preto Dental School, University of Sao Paulo-USP, Ribeirão Preto SP, Brazil.
Sergio L SalvadorDepartment of Clinical Analyses, School of Pharmaceutical Sciences of Ribeirao Preto, University of Sao Paulo-USP, Ribeirão Preto SP, Brazil.
Michel MessoraDepartment of Oral & Maxillofacial Surgery and Periodontology, Ribeirão Preto Dental School, University of Sao Paulo-USP, Ribeirão Preto SP, Brazil.
Daniela B PaliotoDepartment of Oral & Maxillofacial Surgery and Periodontology, Ribeirão Preto Dental School, University of Sao Paulo-USP, Ribeirão Preto SP, Brazil.
Universidade de São Paulo · BRUniversidade de Ribeirão Preto · BR

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESPN°2019/20103-5&FAPESP-BEPE2022/00522-6)
6 · The paper itself

Abstract

objectivesPeriodontal disease is understood to be a result of dysbiotic interactions between the host and the biofilm, causing a unique reaction for each individual, which in turn characterizes their susceptibility. The objective of this study was to chronologically evaluate periodontal tissue destruction induced by systemic bacterial challenge in known susceptible (BALB/c) and resistant (C57BL/6) mouse lineages. MATERIAL AND

methodsAnimals, 6-8 weeks old, were allocated into three experimental groups: Negative control (C), Gavage with sterile carboxymethyl cellulose 2%-without bacteria (Sham), and Gavage with carboxymethyl cellulose 2% + Porphyromonas gingivalis (Pg-W83). Before infection, all animals received antibiotic treatment (sulfamethoxazole/trimethoprim, 400/80 mg/5 mL) for 7 days, followed by 3 days of rest. Microbial challenge was performed 3 times per week for 1, 2, or 3 weeks. After that, the animals were kept until the completion of 42 days of experiments, when they were euthanized. The alveolar bone microarchitecture was assessed by computed microtomography.

resultsBoth C57BL/6 and BALB/c mice exhibited significant bone volume loss and lower trabecular thickness as well as greater bone porosity compared to the (C) and (Sham) groups after 1 week of microbial challenge (p < .001). When comparing only the gavage groups regarding disease implantation, time and lineage, it was possible to observe that within 1 week of induction the disease was more established in BALB/c than in C57BL/6 (p < .05).

conclusionsOur results reflected that after 1 week of microbial challenge, there was evidence of alveolar bone loss for both lineages, with the loss observed in BALB/c mice being more pronounced.

Indexed as

Alveolar Bone LossPeriodontitisAnimalsCarboxymethylcellulose SodiumDisease Models, AnimalMiceMice, Inbred C57BLCarboxymethylcellulose Sodiumalveolar bone losshost microbiota interactionsinflammationperiodontal diseases

Identifiers

PMID37997536
PMCPMC10728515
OpenAlexW4388982514

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.