Evidence map›Paper›PMID 27554451›Full record

ArticleJournal of clinical laboratory analysis2017

The GCKR Gene Polymorphism rs780094 is a Risk Factor for Gestational Diabetes in a Brazilian Population.

Mauren Isfer Anghebem-Oliveira, Susan Webber, Dayane Alberton, Emanuel Maltempi de Souza, Giseli Klassen, Geraldo Picheth, Fabiane Gomes de Moraes Rego

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  13. Molecular Biomarkers for Gestational Diabetes Mellitus.International journal of molecular sciences · 2018
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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 3 institutions in 1 country.

Mauren Isfer Anghebem-OliveiraDepartment of Clinical Analysis, Federal University of Parana, Curitiba, Brazil.
Susan WebberDepartment of Clinical Analysis, Federal University of Parana, Curitiba, Brazil.
Dayane AlbertonDepartment of Clinical Analysis, Federal University of Parana, Curitiba, Brazil.
Emanuel Maltempi de SouzaBiochemistry Department, Federal University of Parana, Curitiba, Brazil.
Giseli KlassenDepartment of Basic Pathology, Federal University of Parana, Curitiba, Brazil.
Geraldo PichethDepartment of Clinical Analysis, Federal University of Parana, Curitiba, Brazil.
Fabiane Gomes de Moraes RegoDepartment of Clinical Analysis, Federal University of Parana, Curitiba, Brazil.ORCID http://orcid.org/0000-0003-1726-8524
Universidade Federal do Paraná · BRPontifícia Universidade Católica do Paraná · BRUniversidade Tecnológica Federal do Paraná · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe glucokinase regulatory protein (GCKR) regulates the activity of the glucokinase (GCK), which plays a key role in glucose homeostasis. Genetic variants in GCK have been associated with diabetes and gestational diabetes (GDM). Due to the relationship between GCKRP and GCK, polymorphisms in GCKR are also candidates for genetic association with GDM. The aim of this study was to evaluate the association between the GCKR rs780094 polymorphism and GDM in a Brazilian population.

methods252 unrelated Euro-Brazilian pregnant women were classified as control (healthy pregnant women, n = 125) and GDM (pregnant women with GDM, n = 127) age-matched groups. Clinical and anthropometric data were obtained from all subjects. The GCKR rs780094 polymorphism was genotyped using fluorescent probes (TaqMan

resultsBoth groups were in Hardy-Weinberg equilibrium. The GCKR rs780094 polymorphism was associated with GDM in codominant and dominant models (P = 0.022 and P = 0.010, respectively). The minor allele (T) frequency for the control group in the study was 38.4% (95% CI: 32-44%), similar to frequencies reported for other Caucasian populations.

conclusionCarriers of the C allele of rs780094 were 1.41 (odds ratio, 95% CI, 0.97-2.03) times more likely to develop GDM.

Indexed as

Genetic Predisposition to DiseaseAdaptor Proteins, Signal TransducingAdultAllelesBrazilDiabetes, GestationalDiabetes Mellitus, Type 2FemaleGene FrequencyGenotypeHumansPolymorphism, Single NucleotidePregnancyRisk FactorsAdaptor Proteins, Signal TransducingGCKR protein, humangenetic associationgenetic polymorphismgestational diabetes mellitusglucokinase regulatory proteinglucose intolerancepregnancy

Identifiers

PMID27554451
PMCPMC6817084
OpenAlexW2509119232

What OpenQuestion holds

Textmetadata
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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.