Perinatal Outcomes in Early and Late Gestational Diabetes Mellitus After Treatment From 24–28 Weeks’ Gestation: A TOBOGM Secondary Analysis

dc.contributor.authorSimmons, Daviden
dc.contributor.authorImmanuel, Jincyen
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, J€Urgenen
dc.contributor.authorBackman, Helenaen
dc.contributor.authorGianatti, Emilyen
dc.contributor.authorSweeting, Arianneen
dc.contributor.authorMohan, Viswanathanen
dc.contributor.authorCheung, N. Wahen
dc.date.accessioned2025-05-23T14:25:05Z
dc.date.available2025-05-23T14:25:05Z
dc.date.issued2024-12-01en
dc.description.abstractIn most gestational diabetes mellitus (GDM) studies, cohorts have included women combined into study populations without regard to whether hyperglycemia was present earlier in pregnancy. In this study we sought to compare perinatal outcomes between groups: women with early GDM (EGDM group: diagnosis before 20 weeks’ gestation but no treatment until 24–28 weeks’ gestation if GDMstill present), with late GDM (LGDM group: present only at 24–28 weeks’ gestation), and with normoglycemia at 24–28 weeks’ gestation (control participants). RESEARCH DESIGN AND METHODS This is a secondary analysis of a randomized controlled treatment trial where we studied, among women with risk factors, early (<20 weeks’ gestation) GDM defined according to World Health Organization 2013 criteria. Those receiving early treatment for GDM treatment were excluded. GDM was treated if present at 24–28 weeks’ gestation. The primary outcome was a composite of birth before 37 weeks’ gestation, birth weight $4,500 g, birth trauma, neonatal respiratory distress, phototherapy, stillbirth/neonatal death, and shoulder dystocia. Comparisons included adjustment for age, ethnicity, BMI, site, smoking, primigravity, and education. RESULTS Women with EGDM(n = 254) and LGDM (n = 467) had shorter pregnancy duration than control participants (n = 2,339). BMI was lowest with LGDM. The composite was increased with EGDM (odds ratio [OR] 1.59, 95% CI 1.18–2.12) but not LGDM (OR 1.19, 95% CI 0.94–1.50). Induction of labor was higher in both GDM groups. In comparisons with control participants there were higher birth centile, higher preterm birth rate, and higher rate of neonatal jaundice for the EGDM group (but not the LGDMgroup). The greatest need for insulin and/or metformin was with EGDM. CONCLUSIONS Adverse perinatal outcomes were increased with EGDM despite treatment from 24–28 weeks’ gestation, suggesting the need to initiate treatment early, and more aggressively, to reduce the effects of exposure to the more severe maternal hyperglycemia from early pregnancy.en
dc.description.sponsorshipThe authors thank the study participants involved in TOBOGM; the trial coordinators, research midwives, and nurses at each site; the maternity service and laboratory staff who assisted with the project; and the trial coordination staff. A full list of members of the TOBOGM Research Group can be found in the APPENDIX below. This study is supported by the National Health and Medical Research Council (grants 1104231 and 2009326), the Region \u20ACOrebro Research Committee (grants Dnr OLL- 970566 and OLL-942177), Medical Scientific Fund of the Mayor of Vienna (project nos. 15205 and 23026), the South Western Sydney Local Health District Academic Unit (grant 2016), and a Western Sydney University Ainsworth Trust Grant (2019). The authors thank the personnel at Roche for the donation of the glucose monitoring meters used by the trial participants.en
dc.description.statusPeer-revieweden
dc.format.extent9en
dc.identifier.issn1935-5548en
dc.identifier.otherPubMed:38421672en
dc.identifier.otherORCID:/0000-0002-6964-3819/work/184100757en
dc.identifier.otherORCID:/0000-0001-6055-5129/work/184103468en
dc.identifier.scopus85197421689en
dc.identifier.urihttp://www.scopus.com/inward/record.url?scp=85197421689&partnerID=8YFLogxKen
dc.identifier.urihttps://hdl.handle.net/1885/733752499
dc.language.isoenen
dc.rightsPublisher Copyright: © 2024 by the American Diabetes Association.en
dc.sourceDiabetes Careen
dc.titlePerinatal Outcomes in Early and Late Gestational Diabetes Mellitus After Treatment From 24–28 Weeks’ Gestation: A TOBOGM Secondary Analysisen
dc.typeJournal articleen
dspace.entity.typePublicationen
local.bibliographicCitation.lastpage2101en
local.bibliographicCitation.startpage2093en
local.contributor.affiliationSimmons, David; Western Sydney Universityen
local.contributor.affiliationImmanuel, Jincy; Western Sydney Universityen
local.contributor.affiliationHague, William M.; University of Adelaideen
local.contributor.affiliationTeede, Helena; Monash Universityen
local.contributor.affiliationNolan, Christopher J.; School of Medicine and Psychology Director's Office, School of Medicine and Psychology, ANU College of Science and Medicine, The Australian National Universityen
local.contributor.affiliationPeek, Michael J.; School of Medicine and Psychology Director's Office, School of Medicine and Psychology, ANU College of Science and Medicine, The Australian National Universityen
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.; University of Sydneyen
local.contributor.affiliationKautzky-Willer, Alexandra; Medical University of Viennaen
local.contributor.affiliationHarreiter, J€Urgen; 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.affiliationCheung, N. Wah; Westmead Hospitalen
local.identifier.citationvolume47en
local.identifier.doi10.2337/dc23-1667en
local.identifier.puref4e433b7-1b65-4c18-86f3-cdbb29cae2cben
local.identifier.urlhttps://www.scopus.com/pages/publications/85197421689en
local.type.statusPublisheden

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