Genetic and Epigenetic Mechanisms of Developing Gestational Diabetes Mellitus and Its Effects on the Fetus
Primary Purpose
Gestational Diabetes Mellitus
Status
Unknown status
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
Life-style modification, insulin therapy if needed
Life-style modification, insulin therapy if needed
Sponsored by
About this trial
This is an interventional basic science trial for Gestational Diabetes Mellitus
Eligibility Criteria
Inclusion Criteria:
- Pregnant women with GDM diagnosed according to the Russian national consensus and the recommendations of the International Association of Diabetes and Pregnancy Study Groups (fasting glucose of ≥5.1 mmol/L, and/or ≥10.0 mmol/L after 1 h, and/or ≥8.5 mmol/L after 2 h in oral glucose tolerance test (OGTT) with 75 g of glucose).
- Gestational age at the time of inclusion in the study 12 weeks 0 days - 31 weeks 6 days
- For control group: pregnant women with normal glucose tolerance confirmed by OGTT at 24-31 weeks of gestation.
Exclusion Criteria:
- Diabetes mellitus type 1 and tipe 2
- Other deseases that affect methabolism of carbohydrates
- Use of drugs that affect methabolism of carbohydrates
- Malformations of the fetus identifired prior to inclusion to the study.
Sites / Locations
- Almazov NMRCRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
No Intervention
Arm Label
very tight glycemic targets
tight-moderate glycemic targets
Control group
Arm Description
Only observation in women with normal glucose tolerance
Outcomes
Primary Outcome Measures
LGA newborns
Number (%) of large for gestational age (LGA) newborns
TRIB1
Level of expression of TRIB1 gene
LEP
Level of expression of LEP gene
ADIPOQ
Level of expression of ADIPOQ gene
ANGPTL4
Level of expression of ANGPTL4 gene
NR3C1
Level of expression of NR3C1 gene
Secondary Outcome Measures
Cesarian sections
Number (%) of deliveries by Cesarian sections
SGA newborns
Number (%) of small for gestationa age (SGA) newborns
Methylation of candidate genes
Levels of methylation (%) of candidate genes with confirmed differences in the expression in HUVECs isolated within 24 hours after delivery
Full Information
NCT ID
NCT03610178
First Posted
November 13, 2017
Last Updated
February 11, 2020
Sponsor
Federal State Budgetary Institution, V. A. Almazov Federal North-West Medical Research Centre, of the Ministry of Health
1. Study Identification
Unique Protocol Identification Number
NCT03610178
Brief Title
Genetic and Epigenetic Mechanisms of Developing Gestational Diabetes Mellitus and Its Effects on the Fetus
Official Title
Genetic and Epigenetic Mechanisms of Developing Gestational Diabetes Mellitus and Its Effects on the Fetus: a Randomised Controlled Trial of Different Glycemic Targets During Pregnancy
Study Type
Interventional
2. Study Status
Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
August 2015 (Actual)
Primary Completion Date
May 2020 (Anticipated)
Study Completion Date
July 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Federal State Budgetary Institution, V. A. Almazov Federal North-West Medical Research Centre, of the Ministry of Health
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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 trialr, open-label.
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Diabetes Mellitus
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Women with GDM are randomised to 2 treatment groups: group 1 - treatment group with very tight glycemic targets (<5.1 mmol / L fasting glucose and <7.0 mmol / l hour after a meal) and group 2 - treatment group with tight-moderate glycemic targets (<5.3 mmol / L fasting glucose and <7.8 mmol / l in an hour after a meal).
Masking
Investigator
Allocation
Randomized
Enrollment
850 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
very tight glycemic targets
Arm Type
Active Comparator
Arm Title
tight-moderate glycemic targets
Arm Type
Active Comparator
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Only observation in women with normal glucose tolerance
Intervention Type
Other
Intervention Name(s)
Life-style modification, insulin therapy if needed
Intervention Description
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
Intervention Type
Other
Intervention Name(s)
Life-style modification, insulin therapy if needed
Intervention Description
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
Primary Outcome Measure Information:
Title
LGA newborns
Description
Number (%) of large for gestational age (LGA) newborns
Time Frame
within 24 hours after delivery
Title
TRIB1
Description
Level of expression of TRIB1 gene
Time Frame
within 24 hours after delivery
Title
LEP
Description
Level of expression of LEP gene
Time Frame
within 24 hours after delivery
Title
ADIPOQ
Description
Level of expression of ADIPOQ gene
Time Frame
within 24 hours after delivery
Title
ANGPTL4
Description
Level of expression of ANGPTL4 gene
Time Frame
within 24 hours after delivery
Title
NR3C1
Description
Level of expression of NR3C1 gene
Time Frame
within 24 hours after delivery
Secondary Outcome Measure Information:
Title
Cesarian sections
Description
Number (%) of deliveries by Cesarian sections
Time Frame
within 24 hours after delivery
Title
SGA newborns
Description
Number (%) of small for gestationa age (SGA) newborns
Time Frame
within 24 hours after delivery
Title
Methylation of candidate genes
Description
Levels of methylation (%) of candidate genes with confirmed differences in the expression in HUVECs isolated within 24 hours after delivery
Time Frame
within 24 hours after delivery
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Gestation
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Pregnant women with GDM diagnosed according to the Russian national consensus and the recommendations of the International Association of Diabetes and Pregnancy Study Groups (fasting glucose of ≥5.1 mmol/L, and/or ≥10.0 mmol/L after 1 h, and/or ≥8.5 mmol/L after 2 h in oral glucose tolerance test (OGTT) with 75 g of glucose).
Gestational age at the time of inclusion in the study 12 weeks 0 days - 31 weeks 6 days
For control group: pregnant women with normal glucose tolerance confirmed by OGTT at 24-31 weeks of gestation.
Exclusion Criteria:
Diabetes mellitus type 1 and tipe 2
Other deseases that affect methabolism of carbohydrates
Use of drugs that affect methabolism of carbohydrates
Malformations of the fetus identifired prior to inclusion to the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Polina Popova, MD, PhD
Phone
+78127550595
Email
pvpopova@yandex.ru
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Griniva Elena, MD, PhD
Organizational Affiliation
Almazov NMRC
Official's Role
Study Director
Facility Information:
Facility Name
Almazov NMRC
City
Saint Petersburg
ZIP/Postal Code
197341
Country
Russian Federation
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Polina Popova, MD, PhD
Phone
+78127025595
Email
pvpopova@yandex.ru
12. IPD Sharing Statement
Plan to Share IPD
No
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Genetic and Epigenetic Mechanisms of Developing Gestational Diabetes Mellitus and Its Effects on the Fetus
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