Evidence map›Paper›PMID 39420427›Full record

ArticleDiabetology & metabolic syndrome2024

The role of incretins in gestational diabetes: a case-control study on the impact of obesity.

Engin Yurtcu, Betul Keyif, Gamze Yilmaz, Selcuk Erkilinc, Hatice Akkaya, A Seval Ozgu-Erdinc

Abstract read
In one paragraph

Article in Diabetology & metabolic syndrome, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Engin YurtcuDepartment of Gynecology and Obstetrics, Faculty of Medicine, Duzce University, Merkez/Düzce, 81620, Turkey. drenginyurtcu1@hotmail.com.
Betul KeyifDepartment of Gynecology and Obstetrics, Faculty of Medicine, Duzce University, Merkez/Düzce, 81620, Turkey.
Gamze YilmazDepartment of Gynecology and Obstetrics, Faculty of Medicine, Duzce University, Merkez/Düzce, 81620, Turkey.
Selcuk ErkilincDepartment of Gynecology and Obstetrics, Faculty of Medicine, Duzce University, Merkez/Düzce, 81620, Turkey.
Hatice AkkayaDepartment of Obstetrics and Gynecology, University of Health Sciences, Ankara Bilkent City Hospital, Ankara, Turkey.
A Seval Ozgu-ErdincDepartment of Obstetrics and Gynecology, University of Health Sciences, Ankara Bilkent City Hospital, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to evaluate the role of serum Glucagon-Like Peptide-1 (GLP-1), Glucagon-Like Peptide-2 (GLP-2), and Glucose-Dependent Insulinotropic Polypeptide (GIP) levels in relation to obesity and gestational diabetes mellitus (GDM) in pregnancy.

methodsA case-control study was conducted, including 96 pregnant women with singleton pregnancies who underwent the Oral Glucose Tolerance Test (OGTT) for GDM diagnosis during the 24th-28th weeks of gestation. Blood samples were collected for measuring GLP-1, GLP-2, GIP, and fasting glucose. Statistical analyses included receiver operating characteristic (ROC) curves and correlation analysis.

resultsAmong the 96 women, no significant difference in age was observed between the groups, but Body Mass Index (BMI) was significantly higher in GDM-O (Gestational Diabetes Mellitus-Obese) and non-GDM-O groups (p < 0.001). GLP-1 had an area under the curve (AUC) of 0.666 (95% CI: 0.553-0.778, p = 0.005) for diagnosing GDM. The optimal GLP-1 cutoff was 815.86 ng/mL, with 65% sensitivity and 77% specificity. A significant correlation was found between GLP-2 and GIP (r = 0.289, p = 0.004), but no significant correlations were observed between GLP-1 and other peptides or gestational age (p > 0.05).

conclusionsImpaired secretion of GLP-1, GLP-2, and GIP likely contributes to the pathogenesis of GDM. GLP-1 may serve as a potential biomarker for diagnosing GDM.

Indexed as

Gestational diabetes mellitusGIPGLP-1GLP-2Incretin

Identifiers

PMID39420427
PMCPMC11487933

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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.