Evidence map›Paper›PMID 23657505›Full record

ArticleHuman genetics2013

Role of TRAV locus in low caries experience.

Jessica Briseño-Ruiz, Takehiko Shimizu, Kathleen Deeley, Piper M Dizak, Timothy D Ruff, Italo M Faraco, Fernando A Poletta, João A Brancher, Giovana D Pecharki, Erika C Küchler and 19 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Human genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Genetic Association ofInternational journal of dentistry · 2017
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. 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

29 authors at 9 institutions in 5 countries.

Jessica Briseño-RuizDepartment of Oral Biology, School of Dental Medicine, University of Pittsburgh, 614 Salk Hall, Pittsburgh, PA, 15261, USA.
Takehiko Shimizu
Kathleen Deeley
Piper M Dizak
Timothy D Ruff
Italo M Faraco
Fernando A Poletta
João A Brancher
Giovana D Pecharki
Erika C Küchler
Patricia N Tannure
Andrea Lips
Thays C S Vieira
Asli Patir
Mine Koruyucu
Juan C Mereb
Judith M Resick
Carla A Brandon
Ariadne Letra
Renato M Silva
Margaret E Cooper
Figen Seymen
Marcelo C Costa
José M Granjeiro
Paula C Trevilatto
Iêda M Orioli
Eduardo E Castilla
Mary L Marazita
Alexandre R Vieira
University of Pittsburgh · USPontifícia Universidade Católica do Paraná · BRUniversidade Federal do Rio de Janeiro · BRUniversidade Federal Fluminense · BRCentro de Educación Médica e Investigaciones Clínicas Norberto Quirno · ARIstanbul University · TRThe University of Texas Health Science Center at Houston · USIstanbul Medipol University · TRNihon University · JP

Funding

Extending the Phenotype of Nonsyndromic Orofacial CleftsR01DE016148 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MARAZITA, MARY L., WEINBERG, SETH M · 2004 to 2018
$19.7M
Genetics of CariesR01DE018914 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VIEIRA, ALEXANDRE REZENDE · 2009 to 2013
$2.2M
NIDCR NIH HHS R01 DE016148NIDCR NIH HHS R01-DE016148NIDCR NIH HHS R01 DE018914
6 · The paper itself

Abstract

Caries is the most common chronic, multifactorial disease in the world today; and little is still known about the genetic factors influencing susceptibility. Our previous genome-wide linkage scan has identified five loci related to caries susceptibility: 5q13.3, 13q31.1, 14q11.2, 14q 24.3, and Xq27. In the present study, we fine mapped the 14q11.2 locus to identify genetic contributors to caries susceptibility. Four hundred seventy-seven subjects from 72 pedigrees with similar cultural and behavioral habits and limited access to dental care living in the Philippines were studied. An additional 387 DNA samples from unrelated individuals were used to determine allele frequencies. For replication purposes, a total of 1,446 independent subjects from four different populations were analyzed based on their caries experience (low versus high). Forty-eight markers in 14q11.2 were genotyped using TaqMan chemistry. Transmission disequilibrium test was used to detect over transmission of alleles in the Filipino families, and Chi-square, Fisher's exact and logistic regression were used to test for association between low caries experience and variant alleles in the replication data sets. We finally assessed the mRNA expression of TRAV4 in the saliva of 143 study subjects. In the Filipino families, statistically significant associations were found between low caries experience and markers in TRAV4. We were able to replicate these results in the populations studied that were characteristically from underserved areas. Direct sequencing of 22 subjects carrying the associated alleles detects one missense mutation (Y30R) that is predicted to be probably damaging. Finally, we observed higher expression in children and teenagers with low caries experience, correlating with specific alleles in TRAV4. Our results suggest that TRAV4 may have a role in protecting against caries.

Indexed as

Base SequenceChromosomes, Human, Pair 14Dental CariesDNA PrimersGene FrequencyGenes, T-Cell Receptor alphaGenetic Association StudiesGenetic LociGenetic Predisposition to DiseaseHumansInheritance PatternsLinkage DisequilibriumLogistic ModelsMolecular Sequence DataMutation, MissensePhilippinesDNA Primers

Identifiers

PMID23657505
PMCPMC3744616
OpenAlexW1969600911

What OpenQuestion holds

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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.