Gestational Diabetes
Conditions
Keywords
gestational diabetes, postpartum, vascular
Brief summary
The purpose of this investigation is to examine the mechanisms mediating vascular dysfunction in women who have had gestational diabetes and how metformin may be a valuable treatment tool to improve microvascular function in these women before the onset of disease.
Detailed description
Women with a history of gestational diabetes mellitus (GDM) are at a 2-fold greater risk for the development of overt cardiovascular disease (CVD) following the effected pregnancy. While subsequent development of type II diabetes elevates this risk, prior GDM is an independent risk factor for CVD morbidity, particularly within the first decade postpartum. GDM is associated with impaired endothelial function during pregnancy and decrements in macro- and microvascular function persist postpartum, despite the remission of insulin resistance following delivery. Collectively, while the association between GDM and elevated lifetime CVD risk is clear, and available evidence demonstrates a link between GDM and vascular dysfunction in the decade following pregnancy, the mechanisms mediating this persistent dysfunction remain unexamined. The purpose of this investigation is to examine the mechanisms mediating vascular dysfunction in women who have had gestational diabetes and how metformin may be a valuable treatment tool to improve microvascular function in these women before the onset of disease. This study will give rise to a new line of research that will center around the goal of improving lifetime cardiovascular outcomes in women with a history of GDM. In this study, the investigators use the blood vessels in the skin as a representative vascular bed for examining mechanisms of microvascular dysfunction in humans. Using a minimally invasive technique (intradermal microdialysis for the local delivery of pharmaceutical agents) they examine the blood vessels in a dime-sized area of the skin in women who have had GDM. Local heating of the skin at the microdialysis sites is used to explore differences in mechanisms governing microvascular control. As a compliment to these measurements, the investigators also draw blood from the subjects and isolate the inflammatory cells.
Interventions
DRUGMetformin Hydrochloride
12 weeks: 850mg metformin once daily for first 7 days then twice daily for the remaining 11 weeks.
OTHERplacebo
12 weeks: placebo tablet once daily for the first 7 days then twice daily for the remaining 11 weeks.
Sponsors
Anna Stanhewicz, PhD
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
* ≥12 weeks and ≤5 years postpartum * history of GDM or healthy pregnancy
Exclusion criteria
* prediabetes or diabetes (HbA1c ≥5.7%) * current tobacco use * cardiovascular or metabolic disease * cardiovascular or metabolic medication * history of hypertension during pregnancy * current pregnancy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| blood flow response to acetylcholine | baseline | cutaneous microvascular dilation (cutaneous conductance ; %max) response to acetylcholine |
| blood flow response to insulin | baseline | cutaneous microvascular dilation (cutaneous conductance ; %max) response to insulin |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Percentage of nitric oxide-dependent dilation | baseline | NO-dependent (%) cutaneous microvascular dilation response to acetylcholine |
| Percentage nitric oxide-dependent dilation | 1 week of treatment | NO-dependent (%) cutaneous microvascular dilation response to acetylcholine |
Countries
United States
Contacts
Primary ContactAnna Stanhewicz, PhD
Outcome results
None listed