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Effect of Metformin on Vascular and Mitochondrial Function in Type 1 Diabetes (MeT1)

21 de diciembre de 2021 actualizado por: University of Colorado, Denver
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.

Descripción general del estudio

Estado

Terminado

Condiciones

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Actual)

23

Fase

  • Fase 4

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Colorado
      • Aurora, Colorado, Estados Unidos, 80045
        • University of Colorado Denver

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

25 años a 59 años (Adulto)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

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:

      1. cancer,
      2. heart failure,
      3. active or end stage liver disease,
      4. kidney disease, or
      5. 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<40 and episodes of this severity >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.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Comparador de placebos: Placebo
Six-week intervention: Study drug/placebo will be given in a forced uptitration with 500 mg once daily for one week, 500 mg twice daily for one week, and then the higher dose (850 mg) for the remainder of the 6 week intervention.
Experimental: Metformina
Six week intervention: Study drug/placebo will be given in a forced uptitration with 500 mg once daily for one week, 500 mg twice daily for one week, 500/1000 for one week, and then 1000mg twice daily for the remainder of the 6 week intervention. If uptitration is not tolerated, max dose will be max tolerated dose of at least 500 mg twice daily.
Otros nombres:
  • glucófago

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Insulin Sensitivity by Hyperinsulinemic Euglycemic Clamp
Periodo de tiempo: End of each 6 week intervention period
Determine the effect of metformin on insulin sensitivity in T1D. Reported measure is glucose infusion rate during hyperinsulinemic euglycemic clamp normalized to total body weight. For this measure, insulin was infused at 40 mU/m2 surface area. Blood sugar wass checked every 5 minutes and glucose infusion adjusted to maintain glucose level at 90 mg/dL for 2 hours. The glucose infusion rate for the final 30 minutes is reported as GIR (aka M-value or glucose disposal rate) in mg glucose/kg*min. A higher value corresponds to greater sensitivity to insulin. There is no strictly defined normal range.
End of each 6 week intervention period
Flow-mediated Brachial Artery Dilation
Periodo de tiempo: End of each 6 week intervention period
Measure of endothelial function by brachial ultrasound of the percent dilation after 5 minutes of occlusion.
End of each 6 week intervention period

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Arterial Stiffness by PWV
Periodo de tiempo: End of each 6 week intervention period
Pulse wave velocity by Sphygmacor as a measure of aortic stiffness in m/sec.
End of each 6 week intervention period
Arterial Stiffness by AI@75
Periodo de tiempo: End of each 6 week intervention period
Augmentation index by Sphygmacor is a measure of aortic arterial stiffness. AI@75 is the ratio of augmented pressure/pulse pressure adjusted to a heart rate of 75.
End of each 6 week intervention period
Mitochondrial Measures: Oxygen Consumption
Periodo de tiempo: End of each 6 week intervention period

Oxygen consumption rate with various substrates and max uncoupled O2 consumption.

Measure is performed on permeabilized muscle fibers from biopsy tissue from the vastus lateralis using the Oroboros OxygraphO2k high resolution respirometer. State 3 is full coupled oxygen flux using PMG or PMGS (pyruvate, malate, glutamate, +/- succinate) or OCMS (octanyl carnitine, malate, +/- succinate) as substrates. state 4 is after addition of oligomycin to inhibit the ATP synthase and thus corresponds to the maximum leak state where O2 consumption is limited by the buildup of the proton gradient and can only proceed as fast as the protons can leak back across the membrane. FCCP is added as an uncoupler, allowing free leakage of protons across the inner membrane, and thus measures maximum possible O2 flux. There are no defined normal ranges, but higher state 3 and uncoupled flux indicate better mitochondrial function, while state 4 is needed to correct state 3 to the fully coupled flux.

End of each 6 week intervention period
Mitochondrial Measures: Protein Expression Levels of Electron Transport Chain Complexes
Periodo de tiempo: End of each 6 week intervention period
Mito content by Western Blotting of electron transport chain complexes I, II, III, and V. complex 1 utilizes NADH from pyruvate/malate/glutamate while complex II utilizes FADH from succinate. complex III is the cytochrome c reductase while complex V is the ATP synthase.
End of each 6 week intervention period
Inflammatory Marker: hsCRP
Periodo de tiempo: End of each 6 week intervention period
hsCRP (mg/L) by Beckman Coulter assay
End of each 6 week intervention period
Heart Rate Variability
Periodo de tiempo: End of each 6 week intervention period
measure of autonomic function: ratio of fastest to slowest heart rate during valsalva maneuver
End of each 6 week intervention period
Continuous Glucose Monitor Measures of Mean Glucose
Periodo de tiempo: Last Week of each 6 Week Intervention Period (over 7 days)
Mean Glucose & Glucose Standard Deviation (Glycemic Variability) by Dexcom CGM
Last Week of each 6 Week Intervention Period (over 7 days)
Continuous Glucose Monitor Measures of Hypoglycemia
Periodo de tiempo: Last Week of each 6 Week Intervention Period (over 7 days)
Percent of time less than 70 mg/dL during the final week of each phase by Dexcom CGM.
Last Week of each 6 Week Intervention Period (over 7 days)
Metabolic Markers: Glucagon
Periodo de tiempo: End of each 6 week intervention period
Glucagon (pg/ml); baseline on AM of each phase final study visit.
End of each 6 week intervention period
Metabolic Markers: Glucose, Triglycerides, Cholesterol
Periodo de tiempo: End of each 6 week intervention period
Glucose (mg/dL), triglycerides (mg/dL), cholesterol (mg/dL) at baseline after each phase
End of each 6 week intervention period
Metabolic Markers: Fatty Acids
Periodo de tiempo: End of each 6 week intervention period
fatty acids (microeq/L) at baseline after each phase in the AM of the final visit
End of each 6 week intervention period
Metabolic Markers: Glycerol
Periodo de tiempo: End of each 6 week intervention period
glycerol (micromol/L) at baseline after each phase in the AM of the final phase visit
End of each 6 week intervention period
Metabolic Markers: Insulin
Periodo de tiempo: End of each 6 week intervention period
insulin (microIU/ml) at baseline after each phase in the AM of the final phase visit
End of each 6 week intervention period
Metabolic Markers: Lactate
Periodo de tiempo: End of each 6 week intervention period
lactate (mmol/L) at baseline after each phase in the AM of the final phase visit
End of each 6 week intervention period
Metabolic Markers: Adiponection
Periodo de tiempo: End of each 6 week intervention period
adiponection (microg/ml) at baseline after each phase in the AM of the final phase visit
End of each 6 week intervention period
Vascular Markers: Endothelin-1 (pg/ml)
Periodo de tiempo: End of each 6 week intervention period
endothelin-1 at baseline after each phase in the AM of the final phase visit by peninsula labs radioimmunoassay
End of each 6 week intervention period
In Vivo Mitochondrial Function: Ratio of the Amount of ATP Generated Per Unit of Oxygen Consumed
Periodo de tiempo: End of each 6 week intervention period
Measured by 31P-mass spec. This ratio measures mitochondrial efficiency. The higher the ratio, the more efficiently the individual converts metabolic substrates into ATP, with the ATP then available for energy-demanding cellular processes such as protein synthesis and biomass production
End of each 6 week intervention period
In Vivo Mitochondrial Function: Time Constants
Periodo de tiempo: End of each 6 week intervention period
Measured by 31P-mass spec. ADP time constant and phosphocreatine time constant. ADP time constant is a measure of the time required to convert ADP → ATP and is a measure of muscle mitochondrial health (energy metabolism). A faster recovery is a better outcome; a slower recovery is a worse outcome. Similarly for phosphocreatine.
End of each 6 week intervention period
In Vivo Mitochondrial Function: QMax, VPCr
Periodo de tiempo: End of each 6 week intervention period

Measured by 31P-mass spec. For each measure, a higher value indicates better mitochondrial function. All re calculated from multiple measures from the MRS spectra. These are relatively new research measures and normal values are not known or generally accepted.

  • QMax is theoretical maximum activity.
  • VPCr measures the rate at which PCr is regenerated.
End of each 6 week intervention period
In Vivo Mitochondrial Function: Oxidative Phosphorylation
Periodo de tiempo: End of each 6 week intervention period
Measured by 31P-mass spec. A higher value indicates better mitochondrial function. All re calculated from multiple measures from the MRS spectra. These are relatively new research measures and normal values are not known or generally accepted. Oxidative Phosphorylation measures the rate at which electron transport activity generates phosphorylated energy sources (ATP and PCr)
End of each 6 week intervention period
In Vivo Mitochondrial Function:AnGly
Periodo de tiempo: End of each 6 week intervention period
Measured by 31P-mass spec. Anaerobic glycolysis measures the amount of anaerobic ATP generation for energy. It is generally felt that a higher value here reflects impaired mitochondrial function necessitating greater reliance on anaerobic metabolism.
End of each 6 week intervention period
Cardiac Function
Periodo de tiempo: End of each 6 week intervention period
Cardiac output
End of each 6 week intervention period

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Vascular Markers: PAI-1
Periodo de tiempo: End of each 6 week intervention period
PAI-1 exploratory thromobotic marker.
End of each 6 week intervention period
Vascular Markers: Exploratory
Periodo de tiempo: End of each 6 week intervention period
ICAM
End of each 6 week intervention period
Oxidative Stress Markers
Periodo de tiempo: End of each 6 week intervention period
TBARs, GSSG:GSH ratio
End of each 6 week intervention period
Mitochondrial Measures: Oxidant Generation
Periodo de tiempo: End of each 6 week intervention period
oxidant generation
End of each 6 week intervention period
Inflammatory Markers: Exploratory
Periodo de tiempo: End of each 6 week intervention period
IL6, TNF alpha
End of each 6 week intervention period
Mitochondrial Oxidant Generation
Periodo de tiempo: after each 6 week intervention
exploratory measure looking at H2O2 production. not performed due to equipment not available.
after each 6 week intervention

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Investigador principal: Irene Schauer, MD, PhD, University of Colorado, Denver

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de junio de 2011

Finalización primaria (Actual)

24 de marzo de 2017

Finalización del estudio (Actual)

24 de marzo de 2017

Fechas de registro del estudio

Enviado por primera vez

28 de septiembre de 2012

Primero enviado que cumplió con los criterios de control de calidad

14 de marzo de 2013

Publicado por primera vez (Estimar)

19 de marzo de 2013

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

21 de enero de 2022

Última actualización enviada que cumplió con los criterios de control de calidad

21 de diciembre de 2021

Última verificación

1 de diciembre de 2021

Más información

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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