Evidence map›Paper›PMID 40912713›Full record

ArticleBMJ open2025

Pancreatic beta-cell secretory products in the diagnosis and risk stratification of gestational diabetes mellitus: a prospective longitudinal cohort study.

Gareth Dunseath, Michael Atkinson, Wai-Yee Cheung, Stephen Luzio, Rajesh Peter

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Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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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

5 authors.

Gareth DunseathDiabetes Research Group, Swansea University Faculty of Medicine Health and Life Science, Swansea, Wales, UK g.j.dunseath@swansea.ac.uk.ORCID http://orcid.org/0000-0001-6022-862X
Michael AtkinsonNeath Port Talbot Hospital, Port Talbot, Wales, UK.
Wai-Yee CheungDiabetes Research Group, Swansea University Faculty of Medicine Health and Life Science, Swansea, Wales, UK.ORCID http://orcid.org/0000-0002-0915-9312
Stephen LuzioDiabetes Research Group, Swansea University Faculty of Medicine Health and Life Science, Swansea, Wales, UK.ORCID http://orcid.org/0000-0002-7206-6530
Rajesh PeterNeath Port Talbot Hospital, Port Talbot, Wales, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGestational diabetes mellitus (GDM) is common in pregnancy and is increasing in prevalence. It is associated with an increased risk of maternal and perinatal complications if not diagnosed and managed early. Most guidelines suggest making a diagnosis of GDM using an oral glucose tolerance test (OGTT) between 24 and 28 weeks of pregnancy at which stage there still is an increased risk of complications. Increased beta-cell secretory product concentrations have been observed prior to changes in glycaemia and can potentially be used as an early marker to diagnose and assess risk of developing GDM.

methodsThe study was a prospective, longitudinal cohort study. OGTTs were carried out at visit one: 16-18 weeks and visit two: 24-28 weeks gestation in pregnant women with at least one risk factor for GDM [Body Mass Index >30 kg/m

resultsUnfortunately, a smaller than planned sample size was recruited due to the start of COVID-19 pandemic midway through the study. 83 pregnant women had OGTT at visit 1. Of these, 12 reached the threshold for GDM at visit 1 and were excluded. In total, data from 66 patients were included for analysis (5 Did Not Attend). Visit 1 hormone comparisons were carried out between 51 who remained NGT and 15 who progressed to GDM at visit 2. There were no significant differences at each time point in ROC AUC between the two groups for total and intact proinsulin and insulin. However, there were significant differences observed in C-peptide ROC AUC at 30 (p=0.041) and 60 min (p=0.003) between the two groups.

conclusionsThis study did not demonstrate significant increase in early proinsulin concentrations in patients that developed GDM. However, there were differences in C-peptide concentrations. The COVID-19 pandemic restricted the recruitment of patient numbers and further studies in a larger cohort will be needed to validate these findings. TRIAL REGISTRATION NUMBER: ISRCTN16416602.

Indexed as

Diabetes, GestationalInsulin-Secreting CellsProinsulinAdultBiomarkersBlood GlucoseCOVID-19C-PeptideFemaleGlucose Tolerance TestHumansInsulinLongitudinal StudiesPregnancyProspective StudiesRisk AssessmentBiomarkersBlood GlucoseC-PeptideInsulinProinsulinDiabetes & endocrinologyDiabetes in pregnancyPregnancy

Identifiers

PMID40912713
PMCPMC12414196

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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.