Evidence map›Paper›PMID 41338933›Full record

ArticleBMJ open diabetes research & care2025

Examining the impact of gestational diabetes genetic susceptibility variants on maternal glucose levels during and post pregnancy.

Aminata H Cissé, Alan Kuang, Catherine Allard, Justiina Ronkainen, Robin N Beaumont, Sylvain Sebert, Denise M Scholtens, Andrew T Hattersley, Marja Vääräsmäki, Eero Kajantie and 7 more

Abstract read
In one paragraph

Article in BMJ open diabetes research & care, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

17 authors.

Aminata H CisséDepartment of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK a.h.cisse@exeter.ac.uk.ORCID http://orcid.org/0000-0003-4984-8494
Alan KuangDepartment of Preventive Medicine, Northwestern University Feinberg School of Medicine, Northwestern University, Evanston, Illinois, USA.
Catherine AllardCentre de Recherche du Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Quebec, Canada.ORCID http://orcid.org/0000-0002-8829-4984
Justiina RonkainenResearch Unit of Population Health, University of Oulu, Oulu, Finland.
Robin N BeaumontDepartment of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.
Sylvain SebertResearch Unit of Population Health, University of Oulu, Oulu, Finland.
Denise M ScholtensDepartment of Preventive Medicine, Northwestern University Feinberg School of Medicine, Northwestern University, Evanston, Illinois, USA.
Andrew T HattersleyDepartment of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.ORCID http://orcid.org/0000-0001-5620-473X
Marja VääräsmäkiResearch Unit of Clinical Medicine, Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.
Eero KajantieResearch Unit of Clinical Medicine, Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.
Luigi BouchardCentre de Recherche du Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Quebec, Canada.ORCID http://orcid.org/0000-0002-7852-0722
Patrice PerronCentre de Recherche du Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Quebec, Canada.ORCID http://orcid.org/0000-0003-4413-6199
Elina KeikkalaResearch Unit of Clinical Medicine, Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.ORCID http://orcid.org/0000-0002-4401-213X
Marie-France HivertCentre de Recherche du Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Quebec, Canada.
William L LoweDepartment of Medicine, Northwestern University Feinberg School of Medicine, Northwestern University, Evanston, Illinois, USA.ORCID http://orcid.org/0000-0001-9467-3422
Alice E HughesDepartment of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.ORCID http://orcid.org/0000-0003-1352-4447
Rachel M FreathyDepartment of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.ORCID http://orcid.org/0000-0003-4152-2238

Funding

Hyperglycemia and Adverse Pregnancy Outcome (HAPO)R01HD034243 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI METZGER, BOYD E · 1999 to 2010
$16.2M
HAPO: DATA COORDINATING CENTERR01HD034242 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DYER, ALAN R · 1999 to 2007
$3.0M
Predicting Newborn and Childhood Adiposity: An Integrated Omics ApproachR01DK117491 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOWE, WILLIAM L, SCHOLTENS, DENISE M · 2018 to 2022
$2.8M
Maternal Obesity and Gestational Diabetes: Impact on MetabolomeR01DK095963 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOWE, WILLIAM L · 2013 to 2016
$1.7M
GWA Mapping: Maternal Metabolism-Birth Weight InteractionsU01HG004415 · NHGRI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOWE, WILLIAM L · 2007 to 2009
$1.1M
NHGRI NIH HHS U01 HG004415NICHD NIH HHS R01 HD034242NICHD NIH HHS R01 HD034243NIDDK NIH HHS R01 DK095963NIDDK NIH HHS R01 DK117491Wellcome Trust
6 · The paper itself

Abstract

aimGenetic variants associated with gestational diabetes mellitus (GDM, n=14 SNPs) were recently classified into two groups: type 2 diabetes predominant effects (Class-T, three SNPs) and GDM-predominant effects (Class-G, eight SNPs; three SNPs unclassified). We aimed to compare the effects of GDM-associated variants on glucose levels (fasting glucose and 2-hour post-OGTT) measured during versus post pregnancy. RESEARCH DESIGN AND

methodsWe calculated genetic scores (GS) by class (T_GS and G_GS) and overall (All_GS) in 10 225 pregnant women and 4763 women post pregnancy (mean 10.5 years post pregnancy) from eight datasets representing four ancestrally-diverse cohorts: Exeter Family Study of Childhood Health, Genetics of Glucose Regulation in Gestation and Growth, Hyperglycaemia and Adverse Pregnancy Outcome, and Finnish Gestational Diabetes. We used linear regression models adjusted for ancestry principal components to investigate associations between standardized GS and glucose levels during or post pregnancy. Analyses were performed separately in each dataset and then combined using inverse-variance weighted random-effects meta-analyses.

resultsAll_GS was associated with fasting glucose both during and post pregnancy (β (95% CI), in mmol/L per 1 SD higher GS=0.06 (0.04 to 0.08) during vs 0.06 (0.04 to 0.07) post pregnancy). All_GS was also associated with 2-hour post-OGTT glucose levels during pregnancy but not after (0.10 (0.04 to 0.15) during vs 0.01 (-0.04 to 0.07) post pregnancy). Both G_GS and T_GS showed consistent associations with fasting glucose during and post pregnancy (0.06 (0.04 to 0.08) during and 0.05 (0.03 to 0.07) post pregnancy for G_GS; 0.02 (0.01 to 0.02) during and 0.02 (-0.001; 0.05) post pregnancy for T_GS). G_GS showed weak evidence of association with 2-hour glucose levels during pregnancy (0.06 (-0.002 to 0.11)) and no association with 2-hour glucose levels post pregnancy (-0.03 (-0.08 to 0.03)). However, T_GS was associated with 2-hour glucose during pregnancy and post pregnancy (0.10 (0.04 to 0.16) and 0.06 (0.01 to 0.12)).

conclusionConsistent associations with fasting glucose levels during and after pregnancy may suggest that biological pathways underlying GDM genetic susceptibility to fasting hyperglycemia are not pregnancy specific. However, the results for All_GS and 2-hour glucose provide evidence that some genetic associations with postprandial glucose may be stronger in pregnancy and should be followed up in larger samples.

Indexed as

BiomarkersBlood GlucoseDiabetes, GestationalGenetic Predisposition to DiseasePolymorphism, Single NucleotidePostpartum PeriodAdultFemaleFollow-Up StudiesGlucose Tolerance TestHumansPregnancyBiomarkersBlood GlucoseCohort StudiesDiabetes, GestationalGeneticsMeta-Analysis

Identifiers

PMID41338933
PMCPMC12682201

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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.