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Association Between Glycemia, Glycemic Variability, and Pregnancy Complications in Early GDM

dc.contributor.authorImmanuel, Jincyen
dc.contributor.authorWah Cheung, N.en
dc.contributor.authorMohajeri, Mahtaen
dc.contributor.authorSimmons, Daniel J.en
dc.contributor.authorHague, William M.en
dc.contributor.authorTeede, Helenaen
dc.contributor.authorNolan, Christopher J.en
dc.contributor.authorPeek, Michael J.en
dc.contributor.authorFlack, Jeff R.en
dc.contributor.authorMcLean, Marken
dc.contributor.authorWong, Vincenten
dc.contributor.authorHibbert, Emily J.en
dc.contributor.authorKautzky-Willer, Alexandraen
dc.contributor.authorHarreiter, Jüurgenen
dc.contributor.authorBackman, Helenaen
dc.contributor.authorGianatti, Emilyen
dc.contributor.authorSweeting, Arianneen
dc.contributor.authorMohan, Viswanathanen
dc.contributor.authorSimmons, Daviden
dc.date.accessioned2025-12-24T08:40:30Z
dc.date.available2025-12-24T08:40:30Z
dc.date.issued2025en
dc.description.abstractOBJECTIVE 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. Over-all, 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 ges-tational 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.en
dc.description.sponsorshipThis study was supported by National Health and Medical Research Council grants 1104231 and 2009326, Region \u00D6Orebro Research Committee grants OLL-970566 and OLL-942177, Medical Scientific Fund of the Mayor of Vienna project numbers 15205 and 23026, South Western Sydney Local Health District Academic Unit grant 2016, and Western Sydney University Ainsworth Trust Grant 2019. Roche Diagnostics provided the glucose meters and funding to cover the expenses associated with meter data extraction. Neither the funding sources nor the author-affiliated institutions took part in the trial de-sign; the collection, analysis, and interpretation of the data; manuscript writing; or decision to submit the manuscript for publication.en
dc.description.statusPeer-revieweden
dc.format.extent7en
dc.identifier.issn0149-5992en
dc.identifier.otherPubMed:39666576en
dc.identifier.otherORCID:/0000-0002-6964-3819/work/195663546en
dc.identifier.otherORCID:/0000-0001-6055-5129/work/195682722en
dc.identifier.scopus85216715944en
dc.identifier.urihttps://hdl.handle.net/1885/733797106
dc.language.isoenen
dc.rights © 2024 by the American Diabetes Association.en
dc.sourceDiabetes Careen
dc.titleAssociation Between Glycemia, Glycemic Variability, and Pregnancy Complications in Early GDMen
dc.typeJournal articleen
dspace.entity.typePublicationen
local.bibliographicCitation.lastpage291en
local.bibliographicCitation.startpage285en
local.contributor.affiliationImmanuel, Jincy; Western Sydney Universityen
local.contributor.affiliationWah Cheung, N.; Westmead Hospitalen
local.contributor.affiliationMohajeri, Mahta; Western Sydney Universityen
local.contributor.affiliationSimmons, Daniel J.; Tectonic Softwareen
local.contributor.affiliationHague, William M.; University of Adelaideen
local.contributor.affiliationTeede, Helena; Monash Universityen
local.contributor.affiliationNolan, Christopher J.; The Australian National Universityen
local.contributor.affiliationPeek, Michael J.; The University of Sydneyen
local.contributor.affiliationFlack, Jeff R.; Bankstown-Lidcombe Hospitalen
local.contributor.affiliationMcLean, Mark; Blacktown Hospitalen
local.contributor.affiliationWong, Vincent; University of New South Walesen
local.contributor.affiliationHibbert, Emily J.; The University of Sydneyen
local.contributor.affiliationKautzky-Willer, Alexandra; Medical University of Viennaen
local.contributor.affiliationHarreiter, Jüurgen; Medical University of Viennaen
local.contributor.affiliationBackman, Helena; Örebro  Universityen
local.contributor.affiliationGianatti, Emily; Fiona Stanley Hospitalen
local.contributor.affiliationSweeting, Arianne; Royal Prince Alfred Hospitalen
local.contributor.affiliationMohan, Viswanathan; Dr. Mohan’s Diabetes Specialities Centre and Madras Diabetes Research Foundationen
local.contributor.affiliationSimmons, David; Western Sydney Universityen
local.identifier.citationvolume48en
local.identifier.doi10.2337/dc24-1199en
local.identifier.pured552c5fd-56af-4643-90ab-5bc124c8ec2een
local.identifier.urlhttps://www.scopus.com/pages/publications/85216715944en
local.type.statusPublisheden

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