Evidence map›Paper›PMID 38198369›Full record

ArticleJournal of applied oral science : revista FOB2024

Dental pain report in children and genetic polymorphism (rs4818) in Catechol-O-Methyltransferase (COMT) gene: a cross- sectional study.

Bruna Leticia Vessoni Menoncin, Aluhê Lopes Fatturi, Rafaela Scariot, José Vitor Nogara Borges Menezes, João Armando Brancher, Juliana Feltrin-Souza

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In one paragraph

Article in Journal of applied oral science : revista FOB, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
2.2field-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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
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

6 authors at 2 institutions in 1 country.

Bruna Leticia Vessoni MenoncinUniversidade Federal do Paraná, Departmento de Estomatologia, Curitiba, PR, Brasil.ORCID http://orcid.org/0000-0002-2417-1213
Aluhê Lopes FatturiUniversidade Federal do Paraná, Departmento de Estomatologia, Curitiba, PR, Brasil.ORCID http://orcid.org/0000-0002-8910-4417
Rafaela ScariotUniversidade Federal do Paraná, Departmento de Estomatologia, Curitiba, PR, Brasil.ORCID http://orcid.org/0000-0002-4911-6413
José Vitor Nogara Borges MenezesUniversidade Federal do Paraná, Departmento de Estomatologia, Curitiba, PR, Brasil.ORCID http://orcid.org/0000-0001-9178-0898
João Armando BrancherUniversidade Positivo, Programa de Pós-Graduação em Odontologia, Curitiba, Brasil.ORCID http://orcid.org/0000-0002-8914-702X
Juliana Feltrin-SouzaUniversidade Federal do Paraná, Departmento de Estomatologia, Curitiba, PR, Brasil.ORCID http://orcid.org/0000-0001-9969-3721
Universidade Federal do Paraná · BRUniversidade Positivo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimPolymorphisms in the COMT gene can alter enzymatic functions, raising levels of endogenous catecholamines, which stimulates beta-adrenergic receptors related to pain. This study aimed to evaluate whether a polymorphism in the COMT gene (rs4818) is associated with dental pain in children. METHODOLOGY: A cross-sectional study was conducted with a representative sample of 731 pairs of children and parents randomly selected from a population-based sample of eight-year-old children. Reports of dental pain was evaluated using a question directed at the parents and self-reported pain using the Faces Pain Scale - Revised. Dental caries experience was determined using the Decayed, Missing, and Filled Teeth (DMFT) index. For genetic analysis, DNA was obtained from oral mucosa epithelial cells of 352 children randomly selected from the initial sample.

resultsChildren with the CC genotype had higher odds of reporting moderate to intense pain than those with the GG genotype (OR=3.60; 95% CI=0.80-16.20; p=0.03). These same children had greater odds of parental reports of pain (OR=1.93; 95% CI=0.91-4.08; p=0.02). Moreover, lower schooling of parents/guardians and caries experience in the primary dentition were significantly associated with greater odds of a parental report of dental pain (OR=2.06; 95% CI=1.47-2.91; p<0.001; OR=6.26; 95% CI=4.46-8.78; p<0.001).

conclusionsThe rs4818 polymorphism of the COMT gene is associated with dental pain. Children with the C allele are more likely to report higher levels of pain. Clinical Relevance: Even though the experience of pain is subjective and multifactorial, this study raises the hypothesis that there is a genetic predisposition to dental pain that should be considered in clinical practice.

Indexed as

Catechol O-MethyltransferaseDental CariesChildCross-Sectional StudiesHumansPainPolymorphism, GeneticCatechol O-MethyltransferaseCOMT protein, human

Identifiers

PMID38198369
PMCPMC10786450
OpenAlexW4390793593

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.