Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Randomized Controlled Trial
. 2023 Oct 24;330(16):1547-1556.
doi: 10.1001/jama.2023.19869.

Early Metformin in Gestational Diabetes: A Randomized Clinical Trial

Affiliations
Randomized Controlled Trial

Early Metformin in Gestational Diabetes: A Randomized Clinical Trial

Fidelma Dunne et al. JAMA. .

Abstract

Importance: Gestational diabetes is a common complication of pregnancy and the optimal management is uncertain.

Objective: To test whether early initiation of metformin reduces insulin initiation or improves fasting hyperglycemia at gestation weeks 32 or 38.

Design, setting, and participants: Double-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.

Interventions: Randomized 1:1 to either placebo or metformin (maximum dose, 2500 mg) in addition to usual care.

Main outcomes and measures: The 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.

Results: Among 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 relevance: Early 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 registration: ClinicalTrials.gov Identifier: NCT02980276; EudraCT: 2016-001644-19.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest Disclosures: Dr Dunne reported nonfinancial support from Merck and matched placebo and nonfinancial support from Ascensia blood glucose–monitoring equipment during the conduct of the study. Dr Devane reported grants from the Health Research Board (HRB). The trial was funded by the HRB of Ireland; coordinated by the HRB-Clinical Research Facility Galway; and nonfinancial support from Merck Healthcare KGaA. Metformin and matched placebo were provided by Merck Healthcare KGaA, Darmstadt, Germany and blood glucose monitoring strips by Ascensia during the conduct of the study. Dr Kgosidialwa reported grants from HRB during the conduct of the study. Dr Finn reported grants from HRB during the conduct of the study. Dr Liew reported receipt of an educational grant to attend international diabetes conference from Novo Nordisk. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. Flow of Patients With Gestational Diabetes Randomized to Metformin vs Placebo
aNumeric values indicating reasons for exclusion are approximate. bSee eBox in Supplement 2 for more information regarding exclusion criteria. cFollow-up information until delivery is not shown for 2 pregnancies because delivery took place outside of Ireland.
Figure 2.
Figure 2.. Time to Insulin Initiation and Fasting Blood Glucose Between Metformin and Placebo Groups
A, Time to first insulin was computed for each patient as the difference in days between the date of randomization and the earlier of the dates of initiation and delivery. Patients who did not receive insulin over this time period were censored at their date of delivery. Significantly fewer patients in the metformin group required insulin over the course of the study (P value calculated using the log-rank test). B, Fasting glucose (approximate distribution) levels were compared between the metformin and placebo groups at randomization, 32 weeks’ gestation, 38 weeks’ gestation, and 12 weeks’ postpartum. The horizontal lines in the boxes indicate the mean, lower and upper ends of the boxes indicate the first and third quartiles, whiskers indicate values within 1.5× the IQR from the upper or lower quartile, and data more extreme than the whiskers are plotted individually as circles. Mean fasting glucose at randomization was very similar between groups. However, the mean fasting glucose level decreased faster in the metformin group than the placebo group resulting in significant differences at 32 and 38 weeks. These differences were small compared with the standard deviation/IQR of fasting glucose at each time point. To convert glucose levels to mg/dL, divide values by 0.0555.

Comment in

References

    1. World Health Organization . Diagnostic criteria and classification of hyperglycaemia first detected in pregnancy. Published January 1, 2013. Accessed July 1, 2023. https://www.who.int/publications/i/item/WHO-NMH-MND-13.2 - PubMed
    1. Yuen L, Saeedi P, Riaz M, et al. Projections of the prevalence of hyperglycaemia in pregnancy in 2019 and beyond: results from the International Diabetes Federation Diabetes Atlas, 9th edition. Diabetes Res Clin Pract. Published online September 10, 2019. doi: 10.1016/j.diabres.2019.107841 - DOI - PubMed
    1. O’Sullivan EP, Avalos G, O’Reilly M, Dennedy MC, Gaffney G, Dunne F; Atlantic DIP Collaborators . Atlantic Diabetes in Pregnancy (DIP): the prevalence and outcomes of gestational diabetes mellitus using new diagnostic criteria. Diabetologia. 2011;54(7):1670-1675. doi: 10.1007/s00125-011-2150-4 - DOI - PubMed
    1. Metzger BE, Lowe LP, Dyer AR, et al. ; HAPO Study Cooperative Research Group . Hyperglycemia and adverse pregnancy outcomes. N Engl J Med. 2008;358(19):1991-2002. doi: 10.1056/NEJMoa0707943 - DOI - PubMed
    1. Fu J, Retnakaran R. The life course perspective of gestational diabetes: an opportunity for the prevention of diabetes and heart disease in women. EClinicalMedicine. 2022;45:101294. doi: 10.1016/j.eclinm.2022.101294 - DOI - PMC - PubMed

Publication types

Associated data