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- Essai clinique NCT00639613
The Role of Small Intestinal Endocrine Cells in Type 2 Diabetic Hyperglucagonemia (T2DM-PC1-2)
25 juin 2015 mis à jour par: 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.
Aperçu de l'étude
Statut
Complété
Les conditions
Intervention / Traitement
Description détaillée
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.
Type d'étude
Observationnel
Inscription (Réel)
20
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
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Copenhagen County
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Hellerup, Copenhagen County, Danemark, 2900
- Department of Internal Medicine F' laboratory
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Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
35 ans et plus (Adulte, Adulte plus âgé)
Accepte les volontaires sains
Oui
Sexes éligibles pour l'étude
Tout
Méthode d'échantillonnage
Échantillon non probabiliste
Population étudiée
Patients with type 2 diabetes
La description
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 d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
|---|---|
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2
Sujets sains
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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.
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Les enquêteurs
- Chercheur principal: Filip K Knop, MD PhD, Department of Internal Medicine
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude
1 mars 2008
Achèvement primaire (Réel)
1 juin 2015
Dates d'inscription aux études
Première soumission
12 mars 2008
Première soumission répondant aux critères de contrôle qualité
12 mars 2008
Première publication (Estimation)
20 mars 2008
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
26 juin 2015
Dernière mise à jour soumise répondant aux critères de contrôle qualité
25 juin 2015
Dernière vérification
1 juin 2015
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- H-B-2007-031
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .