Abstract

BackgroundAnnually in the US, over 100,000 pregnant women with overt type 2 diabetes give birth. Strict maternal glycemic control is the key to optimizing infant outcomes. Medical treatment of type 2 diabetes in pregnancy is generally restricted to insulin, as data on the safety and efficacy of oral hypoglycemic agents in pregnancy are limited. However, over one-third of infants born to women with type 2 diabetes experience an adverse outcome, such as premature delivery, large-for-gestational age, hypoglycemia, hyperbilirubinemia, or birth trauma, suggesting that current treatment regimens fall short of optimizing outcomes. Metformin is the pharmacologic treatment of choice for type 2 diabetes outside of pregnancy. Metformin is favored over insulin because it results in less weight gain, fewer hypoglycemic episodes, and is administered orally rather than injected. However, metformin is not typically used for treatment of type 2 diabetes complicating pregnancy, mainly because no large clinical studies have been conducted to examine its use in this context.Methods/designThis is a randomized double-blind multi-center clinical trial of insulin plus metformin versus insulin plus placebo for the treatment of type 2 diabetes complicating pregnancy. A total of 1200 women with type 2 diabetes will be randomized between 10 weeks 0 days’ and 20 weeks 6 days’ gestation and followed until 30 days after delivery. Neonate outcomes will be followed until 30 days of age. The primary aim is to compare the effect of insulin and metformin versus insulin and placebo on composite adverse neonatal outcomes, comprising perinatal mortality, preterm delivery, neonatal hypoglycemia, hyperbilirubinemia, large-for-gestational age small for gestational age, low birth weight, and/or birth trauma. Key secondary aims are to compare treatment groups for neonatal fat mass and rate of maternal hypoglycemia. Additional aims are to assess the side effects and safety of insulin and metformin among pregnant women with overt type 2 diabetes and to compare gestational weight gain among women treated with metformin plus insulin versus insulin alone.DiscussionSuccessful completion of this study will result in high-quality, contemporary evidence for management of overt type 2 diabetes complicating pregnancy to improve neonatal outcomes.Trial registrationNCT02932475 (05/17/2016).

Highlights

  • In the United States (US), over 100,000 pregnant women with overt type 2 diabetes give birth

  • Successful completion of this study will result in high-quality, contemporary evidence for management of overt type 2 diabetes complicating pregnancy to improve neonatal outcomes

  • Complications associated with Type 2 diabetes mellitus (T2DM) in pregnancy include preeclampsia (20%), early delivery secondary to medical necessity or spontaneous preterm birth (33%), and small or large-for-gestational age (LGA) infants (30%) [2]

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Summary

Background

Type 2 diabetes mellitus (T2DM) is the most common type of diabetes [1]. In the United States (U.S.), T2DM affects approximately 29.1 million people (9.3%), and, of those 29.1 million, 21.0 million are diagnosed and 8.1 million are undiagnosed [1]. Insulin resistance in T2DM significantly complicates pregnancy, and optimal maternal glucose control is challenging. Complications associated with T2DM in pregnancy include preeclampsia (20%), early delivery secondary to medical necessity or spontaneous preterm birth (33%), and small or large-for-gestational age (LGA) infants (30%) [2]. Additional exploratory secondary outcomes for the mother include maternal weight gain, defined as a change in weight from randomization until time of delivery, adjusted for GA at time of randomization; maternal side-effects such as nausea, vomiting, and diarrhea; maternal compliance determined by pill counts; maternal intention to breast or formula feed; adverse maternal outcomes including death, diabetic ketoacidosis, intensive care unit (ICU) admission, intubation, or renal failure; and maternal obstetrical complications including placental abruption or preeclampsia. Other analyses will assess the role and interactions of clinical, biological, and biophysical factors on the occurrence and severity of maternal and neonatal outcomes

Methods
Hours Postprandial
Findings
Discussion
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