Evidence map›Paper›PMID 38922252›Full record

ArticleBrazilian dental journal2024

Association of defects of enamel with polymorphisms in the vitamin D receptor and parathyroid hormone genes.

Amanda Renostro-Souza, Gabriela Fonseca-Souza, Erika Calvano Küchler, Katia Regina Felizardo Vasconcelos, Juliana Feltrin-Souza, Christian Kirschneck, Mírian Aiko Nakane Matsumoto, Cesar Penazzo Lepri, Maria Angelica Hueb de Menezes Oliveira, Geraldo Thedei Júnior

Abstract read
In one paragraph

Article in Brazilian dental journal, 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
–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

1 citing paper in PubMed.

  1. 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

10 authors.

Amanda Renostro-SouzaDepartment of Biomaterials, University of Uberaba, Uberaba, MG, Brazil.ORCID 0000-0001-9221-7036
Gabriela Fonseca-SouzaDepartment of Stomatology, Federal University of Paraná, Curitiba, PR, Brazil.ORCID 0000-0002-8040-8553
Erika Calvano KüchlerDepartment of Orthodontics, University of Bonn, Welschnonnenstr, Bonn, Germany.ORCID 0000-0001-5351-2526
Katia Regina Felizardo VasconcelosDepartment of Biomaterials, University of Uberaba, Uberaba, MG, Brazil.ORCID 0000-0001-9080-4165
Juliana Feltrin-SouzaDepartment of Stomatology, Federal University of Paraná, Curitiba, PR, Brazil.ORCID 0000-0001-9969-3721
Christian KirschneckDepartment of Orthodontics, University of Bonn, Welschnonnenstr, Bonn, Germany.ORCID 0000-0001-9473-8724
Mírian Aiko Nakane MatsumotoDepartment of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.ORCID 0000-0001-8559-8715
Cesar Penazzo LepriDepartment of Biomaterials, University of Uberaba, Uberaba, MG, Brazil.ORCID 0000-0003-4372-9718
Maria Angelica Hueb de Menezes OliveiraDepartment of Biomaterials, University of Uberaba, Uberaba, MG, Brazil.ORCID 0000-0002-2243-9618
Geraldo Thedei JúniorDepartment of Biomaterials, University of Uberaba, Uberaba, MG, Brazil.ORCID 0000-0002-9271-6721

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This cross-sectional study aimed to investigate the association between developmental defects of enamel (DDE) and single nucleotide polymorphisms (SNPs) in the genes encoding the vitamin D receptor (VDR) and parathyroid hormone (PTH). Orthodontic patients receiving treatment at a dental school were selected through convenience sampling. Intra-oral photographs were used to assess DDE, which were classified according to the criteria proposed by Ghanim et al. (2015) by a single calibrated examiner (Kappa>0.80). Enamel hypoplasia, molar-incisor hypomineralization (MIH), hypomimineralized second primary molar (HSPM), and non-MIH/HSPM demarcated opacities were considered for the analysis. Genomic DNA was extracted from buccal cells. The SNPs in VDR (rs7975232) and PHT (rs694, rs6256, and rs307247) were genotyped using real-time polymerase chain reactions (PCR). Statistical analyses were performed using the PLINK software (version 1.03, designed by Shaun Purcell, EUA). Chi-square or Fisher's exact tests were performed at a significance level of 5%. Ninety-one (n=91) patients (49 females and 42 males) (mean age of 14.1±5.8 years) were included. The frequency of DDE was 38.5% (35 patients). Genotype distributions were in Hardy-Weinberg equilibrium. No significant statistical association was found between DDE and the SNPs evaluated. A borderline association (p=0.09) was observed between DDE and the CC haplotype for SNP rs7975232 in VDR. In conclusion, the selected SNPs in VDR and PTH genes were not associated with DDE in the studied samples.

Indexed as

Dental Enamel HypoplasiaParathyroid HormonePolymorphism, Single NucleotideReceptors, CalcitriolAdolescentChildCross-Sectional StudiesDental EnamelFemaleGenotypeHumansMaleReal-Time Polymerase Chain ReactionParathyroid HormoneReceptors, CalcitriolVDR protein, human

Identifiers

PMID38922252
PMCPMC11196029

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.