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- Ensayo clínico NCT00639613
The Role of Small Intestinal Endocrine Cells in Type 2 Diabetic Hyperglucagonemia (T2DM-PC1-2)
25 de junio de 2015 actualizado por: Filip Krag Knop, University Hospital, Gentofte, Copenhagen
Exspression of Prohormone Convertase 1 and 2 in Small Intestinal Endocrine Mucosa Cells in Patients With Type 2 Diabetes
The purpose of this study is to determine whether excessive secretion of glucagon in type 2 diabetes originates from the pancreatic alpha-cells or endocrine cells in the mucosa of the small intestinal.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Descripción detallada
Hyperglucagonemia contributes significantly to the hyperglycemia characterizing patients with Type 2 diabetes.
Fasting hyperglucagonemia induces hepatic glucose release resulting in elevated fasting levels of plasma glucose.
Furthermore, lack of postprandial suppression of glucagon secretion - exchanged for a paradoxical postprandial hypersecretion of glucagon - results in increased levels of postprandial plasma glucose.
Additionally, type 2 diabetes is characterized by decreased postprandial responses of the insulinotropic (and glucagonostatic) peptide hormone glucagon-like peptide-1 (GLP-1).
Recent studies from our group suggest that the intestines are involved in the diminshed suppression of glucagon following ingestion of nutrients.
Thus, suppression of glucagon during oral glucose ingestion diminishes and reverses to stimulation while suppression during intravenous administered glucose sustains along with development of glucose intolerance.
In the small intestines mucosal endocrine L-cells secrete GLP-1, which is processed from its precursor, proglucagon, by prohormone convertase 1 (PC1).
In the pancreatic alpha-cells proglucagon is processed to glucagon via prohormone convertase 2 (PC2).
We plan to examine biopsies from the mucosa of the small intestines from patients with type 2 diabetes and from healthy subjects for glucagon production.
Furthermore, the volunteers will be subjected to a standard meal test in order to correlate the gene expression studies with the level of postprandial hyperglucagonemia of the subjects.
Tipo de estudio
De observación
Inscripción (Actual)
20
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
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Copenhagen County
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Hellerup, Copenhagen County, Dinamarca, 2900
- Department of Internal Medicine F' laboratory
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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
35 años y mayores (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
Sí
Géneros elegibles para el estudio
Todos
Método de muestreo
Muestra no probabilística
Población de estudio
Patients with type 2 diabetes
Descripción
Inclusion Criteria:
- Diagnosed with type 2 diabetes for at least 3 months
- Normal hemoglobin
- Informed consent
Exclusion Criteria:
- Liver disease (ALAT/ASAT > 2 x normal range)
- Diabetic nephropathy (se-creatinin > 130 µM and/or albuminuriu)
- Treatment with medication that can not be stopped for12 hours
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
Cohortes e Intervenciones
Grupo / Cohorte |
Intervención / Tratamiento |
|---|---|
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2
Sujetos sanos
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Double-balloon enteroscopy allows for the entire gastrointestinal tract to be visualized in real time.
The technique involves the use of a balloon at the end of a special enteroscope camera and an overtube, which is also fitted with a balloon.
The procedure is usually done with the use of conscious sedation.
The enteroscope and overtube are inserted through the mouth and passed in conventional fashion (that is, as with gastroscopy) into the small bowel.
Following this, the endoscope is advanced a small distance in front of the overtube and the balloon at the end is inflated.
Using the assistance of friction at the interface of the enteroscope and intestinal wall, the small bowel is accordioned back to the overtube.
The overtube balloon is then deployed, and the enteroscope balloon is deflated.
The process is then continued until the entire small bowel is visualized.
Double-balloon enteroscopy allows for the sampling or biopsying of small bowel mucosa.
Liquid meal consisting of 100 g "Ny NAN" dissolved in 300 ml water (ca.
5000 kJ) to be ingested over 5 minutes.
Blood will be sampled for 4 hours following ingestion.
Samples are centrifuges and plasma will be analysed for glucagon, GLP-1, GIP, insulin and C-peptide concentrations.
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1
Patients with type 2 diabetes
|
Double-balloon enteroscopy allows for the entire gastrointestinal tract to be visualized in real time.
The technique involves the use of a balloon at the end of a special enteroscope camera and an overtube, which is also fitted with a balloon.
The procedure is usually done with the use of conscious sedation.
The enteroscope and overtube are inserted through the mouth and passed in conventional fashion (that is, as with gastroscopy) into the small bowel.
Following this, the endoscope is advanced a small distance in front of the overtube and the balloon at the end is inflated.
Using the assistance of friction at the interface of the enteroscope and intestinal wall, the small bowel is accordioned back to the overtube.
The overtube balloon is then deployed, and the enteroscope balloon is deflated.
The process is then continued until the entire small bowel is visualized.
Double-balloon enteroscopy allows for the sampling or biopsying of small bowel mucosa.
Liquid meal consisting of 100 g "Ny NAN" dissolved in 300 ml water (ca.
5000 kJ) to be ingested over 5 minutes.
Blood will be sampled for 4 hours following ingestion.
Samples are centrifuges and plasma will be analysed for glucagon, GLP-1, GIP, insulin and C-peptide concentrations.
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Investigadores
- Investigador principal: Filip K Knop, MD PhD, Department of Internal Medicine
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 marzo de 2008
Finalización primaria (Actual)
1 de junio de 2015
Fechas de registro del estudio
Enviado por primera vez
12 de marzo de 2008
Primero enviado que cumplió con los criterios de control de calidad
12 de marzo de 2008
Publicado por primera vez (Estimar)
20 de marzo de 2008
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
26 de junio de 2015
Última actualización enviada que cumplió con los criterios de control de calidad
25 de junio de 2015
Última verificación
1 de junio de 2015
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- H-B-2007-031
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. .