Evidence map›Paper›PMID 28699988›Full record

ArticleArchives of endocrinology and metabolism

Type 2 diabetes-associated genetic variants of FTO, LEPR, PPARg, and TCF7L2 in gestational diabetes in a Brazilian population.

Mauren Isfer Anghebem-Oliveira, Bruna Rodrigues Martins, Dayane Alberton, Edneia Amancio de Souza Ramos, Geraldo Picheth, Fabiane Gomes de Moraes Rego

Open access · diamondAbstract read
In one paragraph

Article in Archives of endocrinology and metabolism. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 3 pooled it
4.1field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 3 syntheses or guidelines pooled it, 49 citations in OpenAlex.

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  10. A Longitudinal Study of the Association between theInternational journal of molecular sciences · 2022
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  12. Journal of personalized medicine · 2022
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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

6 authors at 2 institutions in 1 country.

Mauren Isfer Anghebem-OliveiraDepartamento de Análises Clínicas, Universidade Federal do Paraná (UFPR), Curitiba, PR, Brasil.
Bruna Rodrigues MartinsDepartamento de Análises Clínicas, Universidade Federal do Paraná (UFPR), Curitiba, PR, Brasil.
Dayane AlbertonDepartamento de Análises Clínicas, Universidade Federal do Paraná (UFPR), Curitiba, PR, Brasil.
Edneia Amancio de Souza RamosDepartamento de Patologia Básica, Universidade Federal do Paraná (UFPR), Curitiba, PR, Brasil.
Geraldo PichethDepartamento de Análises Clínicas, Universidade Federal do Paraná (UFPR), Curitiba, PR, Brasil.
Fabiane Gomes de Moraes RegoDepartamento de Análises Clínicas, Universidade Federal do Paraná (UFPR), Curitiba, PR, Brasil.
Universidade Federal do Paraná · BRPontifícia Universidade Católica do Paraná · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveGestational diabetes mellitus (GDM) is a metabolic disorder that shares pathophysiologic features with type 2 diabetes mellitus. The aim of this study was to investigate the association of the polymorphisms fat mass and obesity-associated (FTO) rs1421085, leptin receptor (LEPR) rs1137100, rs1137101, peroxisome proliferator-activated receptor gamma (PPARg) rs1801282, and transcription factor 7-like 2 (TCF7L2) rs7901695 with GDM. SUBJECTS AND

methods252 unrelated Euro-Brazilian pregnant women were classified into two groups according to the 2015 criteria of the American and Brazilian Diabetes Association: healthy pregnant women (n = 125) and pregnant women with GDM (n = 127), matched by age. The polymorphisms were genotyped using fluorescent probes (TaqMan®).

resultsAll groups were in Hardy-Weinberg equilibrium. The genotype and allele frequencies of the studied polymorphisms did not show significant differences between the groups (P > 0.05). In the healthy and GDM groups, the C allele frequencies (95% CI) of the FTO rs1421085 polymorphism were 36.8% [31-43%] and 35.0% [29-41%]; the G allele frequencies (95% CI) of the LEPR rs1137100 polymorphism were 24.8% [19-30%] and 22.8% [18-28%]; the G allele frequencies (95% CI) of the LEPR rs1137101 polymorphism were 43.6% [37-50%] and 42.9% [37-49%]; the G allele frequencies (95% CI) of the PPARg rs1801282 polymorphism were 7.6% [4-11%] and 8.3% [5-12%]; and the C allele frequencies (95% CI) of the TCF7L2 rs7901695 polymorphism were 33.6% [28-39%] and 39.0% [33-45%], respectively.

conclusionThe studied polymorphisms were not associated with GDM in a Brazilian population.

Indexed as

AdultAlpha-Ketoglutarate-Dependent Dioxygenase FTOAnalysis of VarianceAnthropometryBrazilCase-Control StudiesCross-Sectional StudiesDiabetes, GestationalDiabetes Mellitus, Type 2FemaleGene FrequencyGenetic Association StudiesGenotypeHumansObesityPolymorphism, GeneticAlpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humanLEPR protein, humanPPAR gammaReceptors, LeptinTranscription Factor 7-Like 2 Protein

Identifiers

PMID28699988
PMCPMC10118805
OpenAlexW2598239438

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.