This is a randomized controlled trial of different glycemic targets during tratment of women with GDM with assessement of epygenetic aspects of their effects on the fetus and pregnancy outcomes. This study is interventional, randomised controlled trial, open-label.
The study aims to clarify the effect of hyperglycemia and its correction, the level of physical activity and consumption of major macro- and micronutrients by women during pregnancy on DNA methylation and expression of genes involved in neuroendocrine regulation and development of metabolic diseases in offspring, as well as functional characteristics of human umbilical vein endothelial cells (HUVECs). For the purpose of the study women with GDM are randomised to 2 treatment groups per glycemic targets ( very tight and tight-moderate glycemic targets). Data on glycenmic levels during the study and consumption of major macro- and micronutrients will be collected using a mobile application with electronic dairies report forms. This clinical trial record primarily describes the overarching observational cohort study "Genetic and Epigenetic Mechanisms of Developing Gestational Diabetes Mellitus and Its Effects on the Fetus" including women with GDM and healthy pregnant women. Substudy Protocol: A key predefined component of this larger study is an interventional, randomized controlled substudy entitled "Tight versus less tight glycaemic targets for women with gestational diabetes mellitus: a randomised controlled trial" (also known as the GEM GDM Trial). The GEM GDM Trial is an open-label, randomized controlled trial (RCT) that compares the effects of tight (very tight) versus less tight (tight-moderate) glycemic control on maternal and neonatal outcomes in women diagnosed with Gestational Diabetes Mellitus (GDM). Participants from the main GEM cohort who are diagnosed with GDM according to International Association of the Diabetes and Pregnancy Study Groups (IADPSG) criteria are eligible for screening and subsequent randomization into this substudy. The substudy aims to enroll 650 pregnant women with a singleton pregnancy and GDM, randomly assigning them in a 1:1 ratio to one of two glycemic target groups. * Tight Target Group: Fasting capillary glucose \<5.1 mmol/L (\<92 mg/dL); 1-hour postprandial glucose \<7.0 mmol/L (\<126 mg/dL). * Less Tight Target Group: Fasting capillary glucose \<5.3 mmol/L (\<95 mg/dL); 1-hour postprandial glucose \<7.8 mmol/L (\<140 mg/dL).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
850
All patients are assigned to life-style modification (diet and physical exercise). If target glucose levels (\<5.1 mmol/L fasting and \<7.0 mmol/L postprandial) are not achieved insulin therapy is started
All patients are assigned to life-style modification (diet and physical exercise). If target glucose levels (\<5.3 mmol/L fasting and \<7.8 mmol/L postprandial) are not achieved insulin therapy is started
Almazov NMRC
Saint Petersburg, Russia
LGA newborns
Number (%) of large for gestational age (LGA) newborns
Time frame: within 24 hours after delivery
TRIB1
Level of expression of TRIB1 gene
Time frame: within 24 hours after delivery
LEP
Level of expression of LEP gene
Time frame: within 24 hours after delivery
ADIPOQ
Level of expression of ADIPOQ gene
Time frame: within 24 hours after delivery
ANGPTL4
Level of expression of ANGPTL4 gene
Time frame: within 24 hours after delivery
NR3C1
Level of expression of NR3C1 gene
Time frame: within 24 hours after delivery
Cesarian sections
Number (%) of deliveries by Cesarian sections
Time frame: within 24 hours after delivery
SGA newborns
Number (%) of small for gestationa age (SGA) newborns
Time frame: within 24 hours after delivery
Methylation of candidate genes
Levels of methylation (%) of candidate genes with confirmed differences in the expression in HUVECs isolated within 24 hours after delivery
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Time frame: within 24 hours after delivery
rate of macrosomia
birth weight ≥4000 g
Time frame: delivery
birthweight
birth weight (g)
Time frame: delivery
length at birth
length at birth (cm)
Time frame: delivery
rate of stillbirth
Foetal death in utero \> 20 weeks
Time frame: > 20 weeks
rate of neonatal death
death \<1 months after delivery
Time frame: 1 month after delivery
rate of shoulder dystocia
vaginal cephalic delivery in which, after the head is delivered and gentle traction proves unsuccessful, additional obstetric maneuvers are required to complete the delivery of the fetus
Time frame: delivery
rate of birth trauma
bone fracture, damage to nerves
Time frame: delivery
rate of preterm birth
babies born at \<37 weeks gestational age
Time frame: delivery
gestational age
gestational age at delivery
Time frame: delivery
rate of neonatal hypoglycemia
plasma glucose level below 2.6 mmol/L within the first 48 hours of age
Time frame: first 48 hours of age
rate of neonatal respiratory distress syndrome
respiratory failure or distress
Time frame: delivery
rate of jaundice
jaundice necessitating phototherapy and/or exchange transfusion
Time frame: delivery
Rate of neonates with Apgar score <7 at 5 minutes
A measure of the health of a newborn infant done at 5 min. The newborn is given points (0, 1, 2) for heart rate, respiratory effort, muscle tone, response to stimulation and skin coloration. A score of 10 points indicates excellent health.
Time frame: delivery
rate of NICU admission
neonatal intensive care unit (NICU) admission
Time frame: within 72 hours postpartum
length of stay of infants admitted to neonatal intensive care unit
length of stay of infants admitted to neonatal intensive care unit, days
Time frame: up to 30 days after delivery
cord blood C-peptide
cord blood C-peptide levels
Time frame: delivery
rate of composite neonatal outcome
infant death, shoulder dystocia, bone fracture, and nerve palsy
Time frame: delivery
rate of maternal death
death of a woman while pregnant or within 42 days of termination of pregnancy
Time frame: within 42 days of termination of pregnancy
rate of eclampsia
generalized convulsions and/or coma
Time frame: from 20 weeks to delivery
rate of placental abruption
premature separation of the placenta from the uterine wall before delivery
Time frame: before delivery
rate of postpartum hemorrhage
requiring or offered blood transfusion or an operative procedure
Time frame: delivery
rate of preeclampsia
onset of new hypertension and proteinuria and/or end-organ dysfunction after 20 weeks of gestation
Time frame: from 20 weeks to delivery
rate of gestational hypertension
new-onset hypertension (140/90 mmHg or higher), without proteinuria after 20 weeks of gestation
Time frame: from 20 weeks to delivery
rate of induction of labor
the use of medications or other methods to bring on (induce) labour
Time frame: delivery
rate of perineal trauma
perineal or deep vaginal laceration
Time frame: delivery
rate of operative vaginal delivery (vacuum extraction)
application of vacuum to the foetal head
Time frame: delivery
gestational weight gain
Weight from preconception until last weight measured within 4 weeks before delivery.
Time frame: delivery
blood pressure at admission to the birth unit
blood pressure at admission to the birth unit, mm Hg
Time frame: at admission to the birth unit
rate of maternal hypoglycemia
typical symptoms with capillary glucose \<3.9 mmol/L, or, if asymptomatic, by capillary glucose \<3.3 mmol/L
Time frame: during pregnancy
insulin therapy requirements
Prescription of insulin treatment
Time frame: from 12 weeks to delivery
rate of stroke
Maternal sudden loss of brain function due to blocked or burst blood vessels during pregnancy or postpartum.
Time frame: during pregnancy or within 42 days after delivery
rate of acute pulmonary oedema
Maternal acute pulmonary oedema
Time frame: During pregnancy of within 42 days after delivery
rate of cardiac arrest
Maternal cardiac arrest
Time frame: During pregnancy or within 42 days after delivery
rate of maternal respiratory arrest
Time frame: During pregnancy or within 42 days after delivery
rate of maternal respiratory distress syndrome
Time frame: During pregnancy or within 42 days after delivery
rate of maternal deep vein thrombosis or pulmonary embolus requiring anticoagulant therapy
Time frame: During pregnancy or within 42 days after delivery
rate of maternal haemolysis
Time frame: During pregnancy or within 42 days after delivery