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- Ensayo clínico NCT02344186
Effects of Liraglutide on ER Stress in Obese Patients With Type 2 Diabetes
Effects of Liraglutide on Endoplasmic (ER) Stress in Obese Patients With Type 2 Diabetes
The main objective of the study will be to test the hypothesis that treatment with Liraglutide will decrease ER stress and adipose tissue in obese patients with type 2 diabetes. Experimental Approach: The investigators will use a prospective, single blind, placebo controlled study design to study 12 obese patients with type 2 diabetes mellitus (T2DM). 6 patients will first receive Liraglutide for 24 weeks followed by placebo for 12 weeks. The other 6 patients will first receive placebo for 12 weeks followed by Liraglutide for 24 weeks.
Measurements: The investigators will determine glycemic control (with HbA1c), body composition (bioelectric impedance analysis), insulin sensitivity (with hyperinsulinemic-euglycemic clamps), insulin secretion (with oral glucose tolerance testing), energy balance (calories in vs. calories out), plasma lipid levels and obtain subcutaneous fat biopsies to determine ER stress response markers before and after placebo and before and after Liraglutide treatment.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
This will be a prospective, single-blind, placebo-controlled study with a crossover design.
Visit Procedures: After a 1 month run-in period during which there will be no changes in medications, physical activity or diet, patients will be randomly divided into 2 groups of 6 patients each. Subjects have a 50:50 chance of being randomized to either group 1 or group 2.
In Group 1, (n=6), liraglutide will be started first with 0.6 mg/d for 1 week, then increased to 1.2 mg/d from week 2 to week 12, followed by 1.8 mg/d from week 12 to week 24. Group 1 patients will then be switched from liraglutide to placebo injections for another 12 weeks. For subjects in Group 1 the placebo period (weeks 24 to 36 will be the washout period.
Group 2 patients (n=6) will be started with placebo for 12 weeks and then switched to liraglutide for the next 24 weeks (0.6 mg/d for 1 week, 1.2 mg/d for 11 weeks and 1.8 mg/d for 12 weeks).
Assessment of Efficacy
Outpatient visits:
During the entire study, all patients (Groups 1 and 2) will perform home glucose monitoring 7 times/day (pre and ~ 2 h post breakfast, lunch and dinner and bedtime) and will be seen at Temple University Hospital as outpatients at 4 week intervals.
One week before the first, second or third and final inpatient visit, patients will undergo a 75, gram 2-hour oral glucose tolerance test.
Inpatient visits:
All patients (Groups 1 and 2) will be studied in our Clinical Research Center (CRC) at Temple University Hospital in the morning after an overnight fast, at the end of the run-in period (Week 0 ) and again at Weeks 12, 24 and 36. All study patients will be admitted to the CRC the evening before their study and discharged in the afternoon of the following day.
During the inpatient visits, the following procedures will be performed.
- At baseline and again at weeks 12 and 36, subcutaneous fat biopsies will be obtained from the lateral aspect of one thigh by a surgeon as described (8) for determination of ER stress markers. In brief, the skin will be cleaned with betadine and anesthetized with 1% lidocaine without epinephrine in a field block pattern (at 2 X 3 in). (We have found that injection of lidocaine too close to the biopsy site interfered with the measurement of acetyl-CoA). After an incision (~ 1 in.) will be made through the skin, ~ 300 mg of fat will be mobilized and excised. The fat will be dropped immediately into isopentane, kept at its freezing point (-160°C) by liquid nitrogen. The frozen fat will be stored at -70°. To screen for changes in unfolded protein response (UPR) genes, we will first perform an UPR PCR microarray (SA Biosciences, Frederick, MD) using pooled fat biopsy extracts. This array profiles expression of 84 key genes recognizing and responding to misfolded protein accumulation in the ER. Significant changes (> 1.5 fold comparing post vs. pre drug biopsies) will then be confirmed by real time reverse transcription (RT)-PCR of the UPR messenger RNAs (mRNAs). Thus, mRNAs of the identified UPR markers (for instance, GRP78, X-box-binding-protein 1 (XBP-1), activating transcription factor 4 (ATF4), activating transcription factor 6 (ATF6), protein disulfide isomerase (PDI), calreticulin, calnexin) will be measured by real time RT-PCR in triplicate and normalized against 18s and β-actin mRNAs and will be expressed as arbitrary units. The respective proteins will be analyzed by Western blots.
Glycemic control will be assessed by
- measurement of HbA1c
- patients home glucose monitoring records
- Determination of insulin resistance will be determined (with euglycemic-hyperinsulinemic clamping with use of stable isotopes for determination of peripheral (GRd) and hepatic (GRa) insulin action as described (18).
- . Determination of energy balance, which will be calculated as change in fat mass (by bioelectric impedance analysis) plus total energy expenditure (determined with indirect calorimetry and the doubly labeled water method) (17).
- Postabsorptive blood samples will be obtained for determination of plasma lipids (total cholesterol, LDL, HDL and triglycerides).
- Assessment of changes in insulin secretion will be determined with Oral Glucose Tolerance Testing.
Tipo de estudio
Inscripción (Anticipado)
Fase
- Fase 4
Contactos y Ubicaciones
Ubicaciones de estudio
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Pennsylvania
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Philadelphia, Pennsylvania, Estados Unidos, 19140
- Temple University Hospital
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Patients with established type 2 diabetes, BMI 27-35, Age - 18-75 years, HbA1c 7-10%, patients treated with exercise, diet, metformin and/or alpha glucosidase inhibitors (all up to ½ of their maximal dose) or pioglitazone (up to 30 mg/d), ability to provide informed consent before any trial-related activities.
Exclusion Criteria:
- Patients with pancreatitis or a history of pancreatitis, patients with HbA1c < 7% or > 10%, type 2 diabetic patients treated with insulin, sulfonylureas, meglitinides, dipeptidyl peptidase-4 (DPP4) inhibitors, glucagon-like peptide-1 (GLP1) agonists or corticosteroids, patients with hypoglycemia unawareness and with impaired liver functions (≥ 2.5 times the upper normal limit), known or suspected allergy against liraglutide or contraindications to liraglutide (as specified in the product prescribing information), pregnancies, breastfeeding or intention of becoming pregnant or not using adequate contraceptive measures, patients with a personal or family history of medullary thyroid cancer and patients with Multiple Endocrine Neoplasia type 2.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Otro
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación cruzada
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
---|---|
Experimental: Liraglutide
Liraglutide will be started first with 0.6 mg/d for 1 week, then increased to 1.2 mg/d from week 2 to week 12, followed by 1.8 mg/d from week 12 to week 24.
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Crossover design - 24 weeks on active drug and 12 weeks daily placebo
Otros nombres:
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Comparador de placebos: Placebo
Subjects will receive placebo for 12 weeks.
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Crossover design - 24 weeks on active drug and 12 weeks daily placebo
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Changes in unfolded protein response markers
Periodo de tiempo: baseline, 6 months, 9 months
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Changes in unfolded protein response markers in adipose tissue biopsy samples.
Specifically, the investigators will determine changes in mRNA (by RT-PCR) and protein (by Western blots) levels of the following ER stress markers: GRP78, ATF4, XBP-1s, PDI, calreticulin and calnexin.
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baseline, 6 months, 9 months
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Insulin sensitivity
Periodo de tiempo: baseline, 3 months, 6 months and 9 months
|
Changes in insulin resistance will be determined by measuring changes in total body glucose uptake and in plasma free fatty acid (FFA) levels during euglycemic-hyperinsulinemic clamping.
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baseline, 3 months, 6 months and 9 months
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Glucose control
Periodo de tiempo: baseline, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months
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Glucose control will be assessed by monthly A1c determinations.
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baseline, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months
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Energy expenditure
Periodo de tiempo: baseline, 3 months, 6 months, 9 months
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Changes in energy expenditure will be assessed by indirect calorimetry
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baseline, 3 months, 6 months, 9 months
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Body weight
Periodo de tiempo: baseline, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months
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Patients will be weighed monthly
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baseline, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months
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Body composition
Periodo de tiempo: baseline, 3 months, 6 months and 9 months
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Body composition will be determined using bioelectrical impedance.
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baseline, 3 months, 6 months and 9 months
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Beta cell function
Periodo de tiempo: baseline, 6 months, 9 months
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Subjects will undergo an oral glucose tolerance tests(OGTT) to assess beta cell function.
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baseline, 6 months, 9 months
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Ajaykumar D Rao, MD, Temple University
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Anticipado)
Finalización del estudio (Anticipado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 21440
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