Phase 4
N=17
Effect of Metformin on Vascular and Mitochondrial Function in Type 1 Diabetes
Type 1 Diabetes
Bottom Line
View on ClinicalTrials.gov: NCT01813929 ↗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
| Outcome | Result | p-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.
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.