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Gestational Diabetes Mellitus and Cardiometabolic Syndrome in Offspring

Is Gestational Diabetes Mellitus (GDM) an Independent Risk Factor for Cardiometabolic Syndrome in Offspring?

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01490372
Acronym
DG3
Enrollment
41
Registered
2011-12-13
Start date
2011-08-31
Completion date
2013-05-31
Last updated
2018-05-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gestational Diabetes Mellitus

Brief summary

Gestational Diabetes Mellitus (GDM) has long been known as leading to macrosomias, neonatal hypoglycemias and other complications which are treatable and preventable. Nowadays, GDM is recognized as an entity with long-term serious sequels to the mother (GDM is considered a forerunner of type 2 diabetes) and her offspring. Indeed, according to the programming hypothesis, GDM sets the stage for metabolic syndrome, obesity, type 2 diabetes and hypertension. However, these cross-sectional studies failed to control for maternal disease history and genetic background although heredity is a major epidemiology risk factor of type 2 diabetes. Also, studies usually refer to traditional markers such as BMI, blood pressure, lipids profile and oral glucose tolerance test (OGTT); none explored inflammatory biomarkers and adipokines in-depth, despite the possible link between their presence and the development of metabolic and cardiovascular diseases in GDM offsprings. Exclusion of genetic confounding factors will help establish the role of GDM as an independent marker of cardiometabolic risk in GDM offspring. It is highly relevant to identify GDM as a risk factor for cardiometabolic diseases, given the worldwide obesity epidemic, the alarming prevalence increase of GDM and its serious sequels to both mother and offspring.

Interventions

None listed

Sponsors

Eli Lilly and Company
CollaboratorINDUSTRY
Université de Sherbrooke
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
4 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* age 4 to 12 years * Tanner stage \< 2 * to understand French or English

Exclusion criteria

* Type 1 diabetes * weight \< 10 kg * placenta abnormalities * gestational age \< 34 weeks * illness affecting growth and metabolism * taking medications

Design outcomes

Primary

MeasureTime frameDescription
Metabolic syndrome4 to 12 years after birth.Prevalence of metabolic syndrome

Secondary

MeasureTime frameDescription
Inflammatory markersAssessed only once 4 to 12 years after birth4 to 12 years after birth.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026