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Metformin for the Treatment of Microvascular Dysfunction After Gestational Diabetes

Early Phase 1
Recruiting
Conditions
Gestational Diabetes
Interventions
Registration Number
NCT05917587
Lead Sponsor
Anna Stanhewicz, PhD
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.

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
30
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
placeboplacebo-
metforminMetformin Hydrochloride-
Primary Outcome Measures
NameTimeMethod
blood flow response to insulin12 weeks of treatment

cutaneous microvascular dilation (cutaneous conductance ; %max) response to insulin

blood flow response to acetylcholine12 weeks of treatment

cutaneous microvascular dilation (cutaneous conductance ; %max) response to acetylcholine

Secondary Outcome Measures
NameTimeMethod
Percentage nitric oxide-dependent dilation1 week of treatment

NO-dependent (%) cutaneous microvascular dilation response to acetylcholine

Percentage of nitric oxide-dependent dilation12 weeks of treatment

NO-dependent (%) cutaneous microvascular dilation response to acetylcholine

Trial Locations

Locations (1)

University of Iowa

🇺🇸

Iowa City, Iowa, United States

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