Evidence map›Paper›PMID 39031189›Full record

Observational studyActa diabetologica2025

Fetal size monitoring in women with gestational diabetes and normal glucose tolerance.

Kaat Beunen, Frederik Van den Abbeele, Paul Van Crombrugge, Johan Verhaeghe, Sofie Vandeginste, Hilde Verlaenen, Toon Maes, Els Dufraimont, Nele Roggen, Christophe De Block and 9 more

Registry-linked trialAbstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study in Acta diabetologica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02036619 (Prospective and Multi-centric Study on Diabetes During Pregnancy in Belgium), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

NCT02036619 completednot on this map

Prospective and Multi-centric Study on Diabetes During Pregnancy in Belgium

TypeobservationalSponsorUniversitaire Ziekenhuizen KU LeuvenRan2014 to 2018Enrolled2,006ConditionsGestational Diabetes, Diabetes
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Kaat BeunenDepartment of Endocrinology, UZ Leuven, KU Leuven, Herestraat 49, Leuven, 3000, Belgium. kaat.beunen@kuleuven.be.ORCID http://orcid.org/0000-0003-3557-0022
Frederik Van den AbbeeleMedicine, KU Leuven, Herestraat 49, Leuven, 3000, Belgium.
Paul Van CrombruggeDepartment of Endocrinology, Onze Lieve Vrouw (OLV) Hospital Aalst-Asse-Ninove, Moorselbaan 164, Aalst, 9300, Belgium.
Johan VerhaegheDepartment of Obstetrics and Gynecology, UZ Leuven, KU Leuven, Herestraat 49, Leuven, 3000, Belgium.
Sofie VandeginsteDepartment of Obstetrics and Gynecology, Onze Lieve Vrouw (OLV) Hospital Aalst-Asse-Ninove, Moorselbaan, Aalst, 164, 9300, Belgium.
Hilde VerlaenenDepartment of Obstetrics and Gynecology, Onze Lieve Vrouw (OLV) Hospital Aalst-Asse-Ninove, Moorselbaan, Aalst, 164, 9300, Belgium.
Toon MaesDepartment of Endocrinology, Imelda Hospital Bonheiden, Imeldalaan 9, Bonheiden, 2820, Belgium.
Els DufraimontDepartment of Obstetrics and Gynecology, Imelda Hospital Bonheiden, Imeldalaan 9, Bonheiden, 2820, Belgium.
Nele RoggenDepartment of Obstetrics and Gynecology, Imelda Hospital Bonheiden, Imeldalaan 9, Bonheiden, 2820, Belgium.
Christophe De BlockDepartment of Endocrinology-Diabetology-Metabolism, Antwerp University Hospital, Drie Eikenstraat 655, Edegem, 2650, Belgium.
Yves JacquemynDepartment of Obstetrics and Gynecology, Antwerp University Hospital, Drie Eikenstraat 655, Edegem, 2650, Belgium.
Farah MekahliDepartment of Endocrinology, Hospital St Jan Brussel, Kruidtuinlaan 32, Brussel, 1000, Belgium.
Katrien De ClippelDepartment of Obstetrics and Gynecology, Hospital St Jan Brussel, Kruidtuinlaan 32, Brussel, 1000, Belgium.
Annick Van den BruelDepartment of Endocrinology, General Hospital St Jan Brugge, Ruddershove 10, Brugge, 8000, Belgium.
Anne LoccufierDepartment of Obstetrics and Gynecology, General Hospital St Jan Brugge, Ruddershove 10, Brugge, 8000, Belgium.
Annouschka LaenenCenter of Biostatics and Statistical bioinformatics, KU Leuven, Kapucijnenvoer 35 bloc d - box 7001, Leuven, 3000, Belgium.
Roland DevliegerDepartment of Obstetrics and Gynecology, UZ Leuven, KU Leuven, Herestraat 49, Leuven, 3000, Belgium.
Chantal MathieuDepartment of Endocrinology, UZ Leuven, KU Leuven, Herestraat 49, Leuven, 3000, Belgium.
Katrien BenhalimaDepartment of Endocrinology, UZ Leuven, KU Leuven, Herestraat 49, Leuven, 3000, Belgium. katrien.benhalima@uzleuven.be.ORCID http://orcid.org/0000-0002-3325-0263

Funding

Belgian National Lottery Belgian National LotteryFonds Wetenschappelijk Onderzoek Fonds Wetenschappelijk OnderzoekFund of the Academic studies of UZ Leuven Fund of the Academic studies of UZ LeuvenFund Yvonne and Jacques François-de Meurs of the King Baudouin Foundation Fund Yvonne and Jacques François-de Meurs of the King Baudouin Foundation
6 · The paper itself

Abstract

aimsTo monitor fetal size and identify predictors for birthweight in women with gestational diabetes (GDM) and normal glucose tolerance (NGT).

methodsCohort study of 1843 women universally screened for GDM, with routine ultrasounds each trimester. Women with GDM and NGT were categorized in subgroups by birthweight centile.

resultsOf the total cohort, 231 (12.5%) women were diagnosed with GDM. Fetal size, incidence of large-for-gestational age (LGA: 12.3% of GDM vs. 12.9% of NGT, p = 0.822) and small-for-gestational age (SGA) neonates (4.8% of GDM vs. 5.1% of NGT, p = 0.886) were similar between GDM and NGT. GDM women with LGA neonates were more insulin resistant at baseline and had more often estimated fetal weight (EFW) ≥ P90 on the 28-33 weeks ultrasound (p = 0.033) than those with AGA (appropriate-for-gestational age) neonates. Compared to NGT women with AGA neonates, those with LGA neonates were more often obese and multiparous, had higher fasting glycemia, a worse lipid profile, and higher insulin resistance between 24 -28 weeks, with more often excessive gestational weight gain. On the 28-33 weeks ultrasound, abdominal circumference ≥ P95 had a high positive predictive value for LGA neonates in GDM (100%), whereas, in both GDM and NGT, EFW ≥ P90 and ≤ P10 had a high negative predictive value for LGA and SGA neonates (> 88%), respectively.

conclusionsThere were no differences in fetal size throughout pregnancy nor in LGA incidence between GDM and NGT women. EFW centile at 28-33 weeks correlated well with birthweight. This indicates that GDM treatment is effective and targeted ultrasound follow-up is useful. TRIAL REGISTRATION CLINICALTRIALS.GOV: NCT02036619. Registration date: January 15, 2014. https://clinicaltrials.gov/ct2/show/NCT02036619 .

Indexed as

Diabetes, GestationalAdultBirth WeightBlood GlucoseCohort StudiesFemaleFetal MacrosomiaFetal WeightGlucose Tolerance TestHumansInfant, NewbornInfant, Small for Gestational AgeInsulin ResistancePregnancyUltrasonography, PrenatalBlood GlucoseFetal biometryFetal sizeGestational diabetes mellitusLarge-for-gestational ageObstetric ultrasoundPregnancy

Identifiers

PMID39031189

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.