Evidence map›Paper›PMID 31831777›Full record

Trial reportScientific reports2019

WNT gene polymorphisms and predisposition to apical periodontitis.

Letícia Chaves de Souza, Franco Cavalla, Lorena Maili, Gustavo P Garlet, Alexandre R Vieira, Renato M Silva, Ariadne Letra

Open access · goldAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

7 citing papers in PubMed, 14 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

7 authors at 4 institutions in 3 countries.

Letícia Chaves de SouzaDepartment of Endodontics, University of Texas Health Science Center School of Dentistry, Houston, 77054, USA.ORCID http://orcid.org/0000-0002-7057-9850
Franco CavallaCenter for Craniofacial Research, University of Texas Health Science Center School of Dentistry, Houston, 77054, USA.
Lorena MailiDepartment of Pediatrics, University of Texas Health Science Center at Houston McGovern Medical School, Houston, 77030, USA.
Gustavo P GarletDepartment of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Bauru, 17012, Brazil.ORCID http://orcid.org/0000-0002-5071-8382
Alexandre R VieiraDepartment of Oral Biology, University of Pittsburgh, Pittsburgh, 15229, USA.ORCID http://orcid.org/0000-0003-3392-6881
Renato M SilvaDepartment of Endodontics, University of Texas Health Science Center School of Dentistry, Houston, 77054, USA.
Ariadne LetraCenter for Craniofacial Research, University of Texas Health Science Center School of Dentistry, Houston, 77054, USA. Ariadne.M.Letra@uth.tmc.edu.ORCID http://orcid.org/0000-0002-7197-6735
The University of Texas Health Science Center at Houston · USUniversidade de São Paulo · BRThe University of Texas Health Science Center · USUniversity of Pittsburgh · US

Funding

Genetics of CariesR01DE018914 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VIEIRA, ALEXANDRE REZENDE · 2009 to 2013
$2.2M
NIDCR NIH HHS R01 DE018914
6 · The paper itself

Abstract

Single nucleotide polymorphisms (SNPs) in WNT genes may impact gene/protein function and contribute to individual predisposition to apical periodontitis (AP). Here, we investigated the association of SNPs in/nearby WNT3, WNT3A, WNT5A, WNT8A, WNT9B and WNT11 genes with AP using a case-control dataset. Cases were defined as individuals with deep caries and AP (n = 188); controls had deep caries and no AP (n = 230). Genotyping was performed using Taqman chemistry in real time PCR. Data analyses was performed using Fisher Exact tests assuming a Bonferroni correction threshold value of 0.005. Single-SNP association analysis revealed a trend for association with WNT3 rs9890413 genotypes (P = 0.009) under a dominant model and allelic association for WNT3A rs1745420 (P = 0.009). Haplotypes involving WNT3-WNT9B-WNT3A alleles were also significantly associated with AP (P ≤ 0.003). Luciferase reporter assays showed higher transcriptional activity (1.4-fold) with the alternate G allele in rs1745420. Expression of WNT3, WNT3A and WNT5A in AP tissues was significantly higher than in control tissues, and inversely correlated with the expression of SERPINB1, COL1A1 and TIMP1 (P < 0.05). Our results suggest that WNT genes have a role in modulating AP and polymorphisms in these genes may increase susceptibility to AP.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideFemaleHumansMalePeriapical PeriodontitisWnt ProteinsWnt Proteins

Identifiers

PMID31831777
PMCPMC6908593
OpenAlexW2995637058

What OpenQuestion 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 OpenQuestion graph.