Association Between Glycemia, Glycemic Variability, and Pregnancy Complications in Early GDMRobinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.
Monash University, Melbourne, Victoria, Australia.
Canberra Hospital and Australian National University, Canberra, New South Wales, Australia.
Nepean Clinical School, Faculty of Medicine and Health, University of Sydney and Nepean Hospital, Sydney, New South Wales, Australia.
Bankstown-Lidcombe Hospital, Sydney, New South Wales, Australia.
Blacktown Hospital, Sydney, New South Wales, Australia.
Liverpool Hospital, Sydney and University of New South Wales, Sydney, New South Wales, Australia.
Nepean Clinical School, Faculty of Medicine and Health, University of Sydney and Nepean Hospital, Sydney, New South Wales, Australia.
Gender Medicine Unit, Division of Endocrinology and Metabolism, Department of Medicine III, Medical University of Vienna, Vienna, Austria.
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.
Department of Endocrinology, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.
Department of Endocrinology, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.
Dr. Mohan's Diabetes Specialities Centre and Madras Diabetes Research Foundation, Chennai, India.
Western Sydney University, Campbelltown, New South Wales, Australia.
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2025 (English)In: Diabetes Care, ISSN 0149-5992, E-ISSN 1935-5548, Vol. 48, no 2, p. 285-291Article in journal (Refereed) Published
Abstract [en]
OBJECTIVE: To investigate the association of timing of commencing glucose management with glycemia, glycemic variability, and pregnancy outcomes among women with early gestational diabetes mellitus (GDM).
RESEARCH DESIGN AND METHODS: In this substudy among participants of a trial of immediate vs delayed treatment of early GDM diagnosed by 2013 World Health Organization criteria, all women treated immediately and those with delayed diagnosis at 24-28 weeks' gestation (treated as if late GDM) were instructed to monitor capillary blood glucose (BG) four times a day (fasting and 2-h postprandial) until delivery. Optimal glycemia was defined as ≥95% of BG measurements between 70 and 140 mg/dL (3.9-7.8 mmol/L).
RESULTS: Overall, 107,716 BG values were obtained from 329 of 549 (59.9%) women (mean age 32.3 ± 4.9 years, BMI 32.0 ± 8.0 kg/m2, 35% European, gestation at GDM diagnosis 15.2 ± 2.4 weeks). Women treated early (n = 213) showed lower mean glucose (MG) and mean fasting glucose (MFG) compared with those treated late (n = 116) (MG: 5.7 ± 0.4 vs. 5.9 ± 0.5, P < 0.001; MFG: 5.2 ± 0.3 vs. 5.3 ± 0.4, P = 0.004), with greater optimal glycemia (74.6% vs. 59.5%, P = 0.006) and similar glycemic variability. MG was similar from 30 weeks' gestation. Overall, optimal glycemia was achieved in 69% of women and associated with lower birth weight, fewer large-for-gestational-age infants (14.4% vs. 26.7%, P = 0.01), more small-for-gestational-age infants (15.3% vs. 5.9%, P = 0.02), and lower gestational weight gain (4.9 ± 6.4 vs. 7.6 ± 6.2 kg, P = 0.001). Suboptimal glycemia was associated with non-European ethnicity, prior GDM, 1-h glucose at booking oral glucose tolerance test, and insulin use.
CONCLUSIONS: Both early and delayed treatment of early GDM resulted in similar glycemia toward the end of pregnancy. Early treatment was associated with improved glycemia overall.
Place, publisher, year, edition, pages
American Diabetes Association , 2025. Vol. 48, no 2, p. 285-291
National Category
Gynaecology, Obstetrics and Reproductive Medicine Endocrinology and Diabetes
Identifiers
URN: urn:nbn:se:oru:diva-117799DOI: 10.2337/dc24-1199ISI: 001407467600020PubMedID: 39666576Scopus ID: 2-s2.0-85216715944OAI: oai:DiVA.org:oru-117799DiVA, id: diva2:1921042
Funder
Region Örebro County, OLL-970566Region Örebro County, OLL-942177
Note
Funding:
This study is Supported by the National Health and Medical Research Council (grants 1104231 and 2009326), the Region Örebro Research Committee (grants Dnr OLL-970566 and OLL-942177), Medical Scientific Fund of the Mayor of Vienna (project numbers 15205 and 23026), the South Western Sydney Local Health District Academic Unit (grant 2016), and a Western Sydney University Ainsworth Trust Grant (2019). Roche Diagnostics provided the meters and funding to cover the expenses associated with meter data extraction.
2024-12-132024-12-132025-02-14Bibliographically approved