Mode
Text Size
Log in / Sign up
Phase 4 N=17 Randomized Double-blind Treatment

Effect of Metformin on Vascular and Mitochondrial Function in Type 1 Diabetes

Type 1 Diabetes

Enrolled (actual)
17
Serious AEs
0.0%
Results posted
Jan 2022
Primary outcome: Primary: Insulin Sensitivity by Hyperinsulinemic Euglycemic Clamp — 3.27; 3.46 mg/kg/min

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Metformin (Drug); Placebo (Drug)
Age
Adult · 25+ yrs
Sex
All
Sponsor
University of Colorado, Denver
Primary completion
Mar 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Insulin Sensitivity by Hyperinsulinemic Euglycemic Clamp
3.27; 3.46
PRIMARY
Flow-mediated Brachial Artery Dilation
8.19; 7.45
SECONDARY
Arterial Stiffness by PWV
8.64; 8.56
SECONDARY
Arterial Stiffness by AI@75
15.89; 14.96
SECONDARY
Mitochondrial Measures: Oxygen Consumption
28.3; 29.7; 44.3; 41.5; 14.6; 14.0
SECONDARY
Mitochondrial Measures: Protein Expression Levels of Electron Transport Chain Complexes
1436; 1084; 4375; 4201; 10361; 9001
SECONDARY
Inflammatory Marker: hsCRP
2.13; 2.95
SECONDARY
Heart Rate Variability
1.55; 1.42
SECONDARY
Continuous Glucose Monitor Measures of Mean Glucose
162; 163; 64; 68
SECONDARY
Continuous Glucose Monitor Measures of Hypoglycemia
8.4; 7.9
SECONDARY
Metabolic Markers: Glucagon
95.5; 90.2
SECONDARY
Metabolic Markers: Glucose, Triglycerides, Cholesterol
135; 124; 98; 78; 156; 154
SECONDARY
Metabolic Markers: Fatty Acids
531; 446
SECONDARY
Metabolic Markers: Glycerol
95; 87
SECONDARY
Metabolic Markers: Insulin
33.9; 49.1
SECONDARY
Metabolic Markers: Lactate
0.79; 0.75
SECONDARY
Metabolic Markers: Adiponection
13.5; 15.1
SECONDARY
Vascular Markers: Endothelin-1 (pg/ml)
6.3; 5.8
SECONDARY
In Vivo Mitochondrial Function: Ratio of the Amount of ATP Generated Per Unit of Oxygen Consumed
0.152; 0.116
SECONDARY
In Vivo Mitochondrial Function: Time Constants
18.4; 23.3; 32.9; 32.8
SECONDARY
In Vivo Mitochondrial Function: QMax, VPCr
0.42; 0.38; 0.24; 0.19
SECONDARY
In Vivo Mitochondrial Function: Oxidative Phosphorylation
0.19; 0.13
SECONDARY
In Vivo Mitochondrial Function:AnGly
0.22; 0.29
SECONDARY
Cardiac Function
5.52; 4.92

Summary

Insulin resistance (IR) is an important contributor to increased cardiovascular disease risk in type 1 diabetes (T1D). The purpose of this study is to measure the effect of metformin on insulin sensitivity, vascular function and compliance, and mitochondrial function in T1D. The long term goal is to identify novel non-glycemic approaches to managing cardiovascular disease risk in T1D. The results of this study may validate a novel approach to T1D treatment that could significantly improve current management of cardiovascular disease risk in this high risk population.

Eligibility Criteria

Inclusion Criteria

  • Age 20-59 years of age,
  • Type 1 diabetes based on antibody-positivity, rapid persistent conversion to insulin requirement after diagnosis, absent C-peptide, or DKA at diagnosis, or a clinical course consistent with T1D,
  • HbA1c 6.0 - 9.5, and
  • Willing and able to commit to two 6 week-long periods of blinded medication followed by hyperinsulinemic euglycemic clamp, vascular testing, and muscle biopsies.

Exclusion Criteria

  • Any comorbid condition associated with:
  • inflammation,
  • insulin Resistance, or
  • dyslipidemia including:
  • cancer,
  • heart failure,
  • active or end stage liver disease,
  • kidney disease, or
  • rheumatological disease;
  • Tobacco use;
  • Pregnancy or women who are breastfeeding;
  • Steroid use;
  • Scheduled strenuous physical activity >3 days a week;
  • Angina, known CAD, or any other cardiovascular or pulmonary disease;
  • A history of COPD or asthma;
  • Presence of systolic blood pressure >190 at rest or >250 with exercise, or diastolic pressure >95 at rest or >105 with exercise;
  • Untreated thyroid disease;
  • Proteinuria (urine protein >200 mg/dl) or a creatinine > 1.5 mg/dl (males) or 1.4 mg/dL (females), suggestive of severe renal disease;
  • Severe Proliferative retinopathy;
  • Niacin treatment;
  • Administration of experimental agent for T1D within 30 days prior to screening;
  • Recent (prior 6 months) or current metformin or thiazolidenedione use;
  • Hypoglycemia unawareness or recurrent severe hypoglycemia (no symptoms of hypoglycemia with FSBS 1 per week);
  • Weight instability (weight change >5% in last 6 months);
  • History of any organ transplant, including islet cell transplant;
  • Current or prior infection with HIV, hepatitis B or hepatitis C or hepatic -insufficiency (AST or ALT > 2x the upper limits of normal);
  • Any condition, medical or otherwise that would, in the opinion of the investigator, prevent complete participation in the study, or that would pose a significant hazard to the subject;
  • History of substance abuse within the 12 months prior to screening.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01813929). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search