Evidence mapPaperPMID 41369738Full record

ArticleDiabetologia2026

Gestational glycaemia reflects lifelong glycaemia: the Pune Maternal Nutrition Study.

Chittaranjan S Yajnik, Souvik Bandyopadhyay, Dattatray S Bhat, Rucha S H Wagh, Pallavi C Yajnik, Rasika Ladkat, Kurus Coyaji, Caroline H D Fall

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Article in Diabetologia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3 citing papers in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Chittaranjan S YajnikDiabetes Unit, KEM Hospital Research Centre, Pune, India. csyajnik@gmail.com.
Souvik BandyopadhyayCytel Inc., Cambridge, MA, USA.
Dattatray S BhatDiabetes Unit, KEM Hospital Research Centre, Pune, India.
Rucha S H WaghDiabetes Unit, KEM Hospital Research Centre, Pune, India.
Pallavi C YajnikDiabetes Unit, KEM Hospital Research Centre, Pune, India.
Rasika LadkatDiabetes Unit, KEM Hospital Research Centre, Pune, India.
Kurus CoyajiDiabetes Unit, KEM Hospital Research Centre, Pune, India.
Caroline H D FallMRC Lifecourse Epidemiology Centre, University of Southampton, Southampton, UK.

Funding

Department of Biotechnology, Ministry of Science and Technology, India BT/PR-6870/PID/20/268/2005Indian Council of Medical Research 58/1/8/MRC-ICMR/2009/NCD-IIMedical Research Council, UK MR/J000094/1Wellcome Trust, UK 038128/Z/93Wellcome Trust, UK 059609/Z/99Wellcome Trust, UK 079877/Z/06/ZWellcome Trust, UK 083460/Z/07/ZWellcome Trust, UK 098575/B/12/Z
6 · The paper itself

Abstract

aims/hypothesisTraditionally, gestational diabetes mellitus (GDM) (defined here as hyperglycaemia first detected during pregnancy) has been considered to be a transient condition of pregnancy, but evidence suggests it is often a pre-existing chronic condition. Studies have reported that women diagnosed with GDM were hyperglycaemic, obese and insulin-resistant from before pregnancy. However, little is known about the life-course evolution of glycaemia before pregnancy. Participants in the Pune Maternal Nutrition Study (PMNS) birth cohort underwent serial measurements of glycaemia from early childhood, through puberty, young adulthood, pregnancy and later, providing a unique opportunity to test the hypothesis that pregnancy glycaemia (fasting plasma glucose and/or OGTT AUC) is only a window on a lifetime glycaemic trajectory.

methodsFemale participants in the PMNS birth cohort, established in 1993, underwent serial glucose measurements at ages 6, 12 and 18 years, and during pregnancy and post-delivery follow-up. Of 366 female cohort members, 171 became pregnant and delivered by February 2020. Given the small number of GDM cases (n=20, IADPSG criteria), we divided women into quartiles of fasting plasma glucose (FPG) and AUC during an OGTT at 28 weeks' gestation to study life-course tracking of pregnancy glycaemia.

resultsAt 28 weeks' gestation, the women (mean age 20.9 years) had a median BMI of 21.7 kg/m CONCLUSIONS/

interpretationIn this cohort of rural lean Indian women, higher pregnancy glycaemia reflects persistently higher glycaemia since childhood. Coupled with the existing evidence that women with GDM have higher glycaemia from before pregnancy, our results suggest that pregnancy hyperglycaemia is only a window on a life-course of hyperglycaemia and not a de novo phenomenon. This has implications for the timing of diagnosis and management of pregnancy hyperglycaemia (GDM).

Indexed as

Blood GlucoseDiabetes, GestationalHyperglycemiaMaternal Nutritional Physiological PhenomenaAdolescentAdultChildCohort StudiesFastingFemaleGlucose Tolerance TestHumansPregnancyYoung AdultBlood GlucoseGestational glycaemiaIndian subcontinentLife-course glycaemic trajectory

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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 Socratic graph.