Relationship Between Early-Pregnancy Glycemia and Adverse Outcomes: Findings From the TOBOGM Study.


Journal

Diabetes care
ISSN: 1935-5548
Titre abrégé: Diabetes Care
Pays: United States
ID NLM: 7805975

Informations de publication

Date de publication:
31 Jul 2024
Historique:
received: 17 11 2023
accepted: 30 05 2024
medline: 31 7 2024
pubmed: 31 7 2024
entrez: 31 7 2024
Statut: aheadofprint

Résumé

We evaluated associations between early-pregnancy oral glucose tolerance test (OGTT) glucose and complications in the Treatment of Booking Gestational Diabetes Mellitus (TOBOGM) cohort to inform prognostic OGTT thresholds. Individuals with risk factors for hyperglycemia were recruited for an international, multicenter, randomized controlled gestational diabetes mellitus (GDM) (World Health Organization 2013 criteria) treatment trial. A 2-h 75-g OGTT was performed at <20 weeks' gestation. Individuals with early treated hyperglycemia in pregnancy were excluded from the primary analysis. Early OGTT glucose concentrations were analyzed continuously and in glycemic categories (normal, low band, and high band). Overall, 3,645 individuals had an OGTT at (mean ± SD) 15.6 ± 2.5 weeks. For each 1-SD increase in fasting, 1-h, and 2-h glucose values, there were continuous positive associations with late GDM: adjusted odds ratio (aOR) 2.04 (95% CI 1.82-2.27), 3.05 (2.72-3.43), and 2.21 (1.99-2.45), respectively. There were continuous positive associations between 1-h and 2-h glucose and the perinatal composite (birth <37 + 0 weeks, birth trauma, birth weight ≥4,500 g, respiratory distress, phototherapy requirement, stillbirth/neonatal death, and shoulder dystocia), with aOR 1.15 (95% CI 1.04-1.26) and 1.14 (1.04-1.25), respectively, and with large-for-gestational-age offspring, with aOR 1.18 (1.06-1.31) and 1.26 (1.01-1.25), respectively. Significant associations were also observed between 1-h glucose and cesarean section and between fasting and 2-h glucose and neonatal hypoglycemia. In categorical analysis, only the high-band 1-h glucose (≥10.6 mmol/L [191 mg/dL]) predicted the perinatal composite. There is a continuous positive association between early-pregnancy OGTT glucose and complications. In individuals with hyperglycemia risk factors, only the high-glycemic-band 1-h glucose corresponded to increased risk of major perinatal complications.

Identifiants

pubmed: 39083673
pii: 157032
doi: 10.2337/dc23-2214
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Western Sydney University Ainsworth Trust Grant 2019
Organisme : Region Örebro Research Committee
ID : OLL-942177
Organisme : Medical Scientific Fund of the Mayor of Vienna
ID : 15205
Organisme : South Western Sydney Local Health District Academic Unit 2016
Organisme : National Health and Medical Research Council
ID : 1104231
Organisme : Australian Diabetes Association Skip Martin Early Career Fellowship

Informations de copyright

© 2024 by the American Diabetes Association.

Auteurs

Arianne Sweeting (A)

Department of Endocrinology, Royal Prince Alfred Hospital and University of Sydney, Sydney, New South Wales, Australia.

Joanne Enticott (J)

Monash University, Melbourne, Victoria, Australia.

Jincy Immanuel (J)

Western Sydney University, Campbelltown, New South Wales, Australia.

William M Hague (WM)

Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.

Helena Teede (H)

Monash University, Melbourne, Victoria, Australia.

Christopher J Nolan (CJ)

Canberra Hospital and Australian National University, Canberra, Australia Capital Territory, Australia.

Michael J Peek (MJ)

Australian National University, Canberra, Australia Capital Territory, Australia.

Jeff R Flack (JR)

Bankstown-Lidcombe Hospital, Sydney, New South Wales, Australia.

Mark McLean (M)

Blacktown Hospital, Blacktown, New South Wales, Australia.

Vincent W Wong (VW)

Liverpool Hospital and University of New South Wales, Sydney, New South Wales, Australia.

Emily J Hibbert (EJ)

Nepean Clinical School, University of Sydney, and Nepean Hospital, Sydney, New South Wales, Australia.

Alexandra Kautzky-Willer (A)

Gender Medicine Unit, Division of Endocrinology and Metabolism, Department of Medicine III, Medical University of Vienna, Vienna, Austria.

Jürgen Harreiter (J)

Gender Medicine Unit, Division of Endocrinology and Metabolism, Department of Medicine III, Medical University of Vienna, Vienna, Austria.
Department of Medicine, Landesklinikum Scheibbs, Scheibbs, Austria.

Helena Backman (H)

Department of Obstetrics and Gynecology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.

Emily Gianatti (E)

Department of Endocrinology, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.

Viswanathan Mohan (V)

Dr. Mohan's Diabetes Specialities Centre and Madras Diabetes Research Foundation, Chennai, India.

N Wah Cheung (NW)

Westmead Hospital and University of Sydney, Sydney, New South Wales, Australia.

David Simmons (D)

Western Sydney University, Campbelltown, New South Wales, Australia.

Classifications MeSH