Evidence map›Paper›PMID 30014583›Full record

Trial reportMolecular genetics & genomic medicine2018

Frequency of HLA-DQ, susceptibility genotypes for celiac disease, in Brazilian newborns.

Fernanda C Almeida, Lenora Gandolfi, Karina N Costa, Marilucia R A Picanço, Lucas M Almeida, Yanna K M Nóbrega, Riccardo Pratesi, Claudia B Pratesi, Nicole Selleski

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Molecular genetics & genomic medicine, 2018. 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
0.3field-weighted citation impact, top 39% 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, 2 citations in OpenAlex.

  1. Trial
  2. Article
  3. Frequency of HLA celiac disease risk alleles and haplotypes in healthy adults in Tamil Nadu.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2019
    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

9 authors at 1 institution in 1 country.

Fernanda C AlmeidaGraduate Program in Medical Sciences, School of Medicine, University of Brasilia, Brasilia, DF, Brazil.
Lenora GandolfiGraduate Program in Medical Sciences, School of Medicine, University of Brasilia, Brasilia, DF, Brazil.
Karina N CostaDepartment of Pediatrics, School of Medicine, University of Brasilia, Brasilia, DF, Brazil.
Marilucia R A PicançoDepartment of Pediatrics, School of Medicine, University of Brasilia, Brasilia, DF, Brazil.
Lucas M AlmeidaGraduate Program in Medical Sciences, School of Medicine, University of Brasilia, Brasilia, DF, Brazil.
Yanna K M NóbregaGraduate Program in Medical Sciences, School of Medicine, University of Brasilia, Brasilia, DF, Brazil.
Riccardo PratesiGraduate Program in Medical Sciences, School of Medicine, University of Brasilia, Brasilia, DF, Brazil.
Claudia B PratesiResearch Center for Celiac Disease, School of Medicine, University of Brasilia, Brasilia, DF, Brazil.
Nicole SelleskiResearch Center for Celiac Disease, School of Medicine, University of Brasilia, Brasilia, DF, Brazil.ORCID 0000-0001-6790-829X
Universidade de Brasília · BR

Funding

Coordenação de Aperfeiçoamento de Pessoal de nível Superior" (CAPES)
6 · The paper itself

Abstract

backgroundThe frequency of HLA-DQ2 and DQ8 predisposing genotypes for celiac disease (CD) has shown significant variation among different world regions and has not been previously determined among the highly interbred Brazilian population. The aim of this study was to investigate the frequency of these genotypes among Brazilian newborns (NB).

methodsWe typed DQA1*05 - DQB1*02 (DQ2.5) and DQA1*03 - DQB1*03:02 (DQ8) alleles in 329 NB using qPCR technique. Subsequently we confirmed our results by PCR-SSP using a reference kit which further identified DQ2.2 (DQA1*02:01 - DQB1*02).

resultsAmong the 329 NB, using qPCR technique: 5 (1.52%) carried both DQ2.5 and DQ8 variants; 58 (17.63%) carried only DQ2.5 (DQA1*05 and DQB1*02) and 47 (14.29%) carried only the DQ8 (DQA1*03 and DQB1*03:02) variant. The use of the PCR-SSP method yielded further information; among the 329 samples: 34 (10.34%) tested positive for DQ2.2 and among the 47 previously DQ8 positives samples, we found 10 (3.04%) that also tested positives for DQ2.2.

conclusion43.7% of the analyzed individual tested positive for at least one of the CD predisposing HLA-DQ genotypes in our group of Brazilian NB. The highest frequency was found for DQ2.5 positive subjects (17.6%) followed by DQ8 (11.3%); DQ2.2 (10.3%); DQ8 and DQ2.2 (3.0%); DQ2.5 and DQ8 (1.5%). We found no positive sample for DQ2.5 associated with DQ2.2.

Indexed as

AllelesGene FrequencyGenetic Predisposition to DiseaseBrazilCeliac DiseaseFemaleHLA-DQ AntigensHumansInfant, NewbornMaleReal-Time Polymerase Chain ReactionHLA-DQ Antigensceliac diseasefrequencyHLA-DQ2HLA-DQ8newbornpolymerase chain reaction

Identifiers

PMID30014583
PMCPMC6160714
OpenAlexW2883865162

What OpenQuestion holds

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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.