Early Metformin in Gestational Diabetes

Author:

Dunne Fidelma123,Newman Christine123,Alvarez-Iglesias Alberto2,Ferguson John2,Smyth Andrew123,Browne Marie2,O’Shea Paula1,Devane Declan14,Gillespie Paddy5,Bogdanet Delia126,Kgosidialwa Oratile17,Egan Aoife18,Finn Yvonne123,Gaffney Geraldine123,Khattak Aftab2,O’Keeffe Derek123,Liew Aaron19,O’Donnell Martin123

Affiliation:

1. College of Medicine Nursing and Health Sciences, University of Galway, Co Galway, Ireland

2. HRB Clinical Research Facility Galway, University of Galway, Co Galway, Ireland

3. Galway University Hospital, Co Galway, Ireland

4. HRB Trials Methodology Research Network, University of Galway, Co Galway, Ireland

5. School of Business and Economics, University of Galway, Co Galway, Ireland

6. Mayo University Hospital, Castlebar, Co Mayo, Ireland

7. Cork University Hospital, Co Cork, Ireland

8. Mayo Clinic, Rochester, Minnesota

9. Portiuncula University Hospital, Portiuncula, Co Galway, Ireland

Abstract

ImportanceGestational diabetes is a common complication of pregnancy and the optimal management is uncertain.ObjectiveTo test whether early initiation of metformin reduces insulin initiation or improves fasting hyperglycemia at gestation weeks 32 or 38.Design, Setting, and ParticipantsDouble-blind, placebo-controlled trial conducted in 2 centers in Ireland (one tertiary hospital and one smaller regional hospital). Participants were enrolled from June 2017 through September 2022 and followed up until 12 weeks’ postpartum. Participants comprised 510 individuals (535 pregnancies) diagnosed with gestational diabetes based on World Health Organization 2013 criteria.InterventionsRandomized 1:1 to either placebo or metformin (maximum dose, 2500 mg) in addition to usual care.Main Outcomes And MeasuresThe primary outcome was a composite of insulin initiation or a fasting glucose level of 5.1 mmol/L or greater at gestation weeks 32 or 38.ResultsAmong 510 participants (mean age, 34.3 years), 535 pregnancies were randomized. The primary composite outcome was not significantly different between groups and occurred in 150 pregnancies (56.8%) in the metformin group and 167 pregnancies (63.7%) in the placebo group (between-group difference, −6.9% [95% CI, −15.1% to 1.4%]; relative risk, 0.89 [95% CI, 0.78-1.02]; P = .13). Of 6 prespecified secondary maternal outcomes, 3 favored the metformin group, including time to insulin initiation, self-reported capillary glycemic control, and gestational weight gain. Secondary neonatal outcomes differed by group, with smaller neonates (lower mean birth weights, a lower proportion weighing >4 kg, a lower proportion in the >90% percentile, and smaller crown-heel length) in the metformin group without differences in neonatal intensive care needs, respiratory distress requiring respiratory support, jaundice requiring phototherapy, major congenital anomalies, neonatal hypoglycemia, or proportion with 5-minute Apgar scores less than 7.Conclusion and relevanceEarly treatment with metformin was not superior to placebo for the composite primary outcome. Prespecified secondary outcome data support further investigation of metformin in larger clinical trials.Trial RegistrationClinicalTrials.gov Identifier: NCT02980276; EudraCT: 2016-001644-19

Publisher

American Medical Association (AMA)

Subject

General Medicine

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