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Development of a glucagon sensitivity test in humans: Pilot data and the GLUSENTIC study protocol.
Kjeldsen, Sasha A S; Richter, Michael M; Jensen, Nicole J; Nilsson, Malin S D; Heinz, Niklas; Nybing, Janus D; Linden, Frederik H; Høgh-Schmidt, Erik; Boesen, Mikael P; Madsbad, Sten; Vilstrup, Hendrik; Schiødt, Frank Vinholt; Møller, Andreas; Nørgaard, Kirsten; Schmidt, Signe; Rashu, Elias B; Gluud, Lise L; Haugaard, Steen B; Holst, Jens J; Rungby, Jørgen; Wewer Albrechtsen, Nicolai J.
Afiliación
  • Kjeldsen SAS; Department of Clinical Biochemistry, Bispebjerg and Frederiksberg Hospital, Bispebjerg, Denmark; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Department of Biomedical Sciences, Faculty of Health and Medica
  • Richter MM; Department of Clinical Biochemistry, Bispebjerg and Frederiksberg Hospital, Bispebjerg, Denmark; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Jensen NJ; Department of Endocrinology, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Nilsson MSD; Department of Endocrinology, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Heinz N; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Nybing JD; Department of Radiology, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Linden FH; Department of Radiology, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Høgh-Schmidt E; Department of Radiology, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Boesen MP; Department of Radiology, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Madsbad S; Department of Endocrinology, Hvidovre University Hospital, Hvidovre, Denmark.
  • Vilstrup H; Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.
  • Schiødt FV; Department of Gastroenterology, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Møller A; Department of Gastroenterology and Gastrointestinal Surgery, Hvidovre University Hospital, Hvidovre, Denmark.
  • Nørgaard K; Institute of Clinical Medicine, Faculty of Health Science, University of Copenhagen, Denmark; Steno Diabetes Center Copenhagen, Herlev, Denmark.
  • Schmidt S; Steno Diabetes Center Copenhagen, Herlev, Denmark.
  • Rashu EB; Department of Gastroenterology and Gastrointestinal Surgery, Hvidovre University Hospital, Hvidovre, Denmark.
  • Gluud LL; Department of Gastroenterology and Gastrointestinal Surgery, Hvidovre University Hospital, Hvidovre, Denmark; Institute of Clinical Medicine, Faculty of Health Science, University of Copenhagen, Denmark.
  • Haugaard SB; Department of Endocrinology, Bispebjerg University Hospital, Copenhagen, Denmark; Institute of Clinical Medicine, Faculty of Health Science, University of Copenhagen, Denmark.
  • Holst JJ; Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Rungby J; Department of Endocrinology, Bispebjerg University Hospital, Copenhagen, Denmark; Steno Diabetes Center Copenhagen, Herlev, Denmark.
  • Wewer Albrechtsen NJ; Department of Clinical Biochemistry, Bispebjerg and Frederiksberg Hospital, Bispebjerg, Denmark; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark. Electronic address: nicolai.albrechtsen@sund.ku.dk.
Peptides ; 161: 170938, 2023 03.
Article en En | MEDLINE | ID: mdl-36596314
ABSTRACT
A physiological feedback system exists between hepatocytes and the alpha cells, termed the liver-alpha cell axis and refers to the relationship between amino acid-stimulated glucagon secretion and glucagon-stimulated amino acid catabolism. Several reports indicate that non-alcoholic fatty liver disease (NAFLD) disrupts the liver-alpha cell axis, because of impaired glucagon receptor signaling (glucagon resistance). However, no experimental test exists to assess glucagon resistance in humans. The objective was to develop an experimental test to determine glucagon sensitivity with respect to amino acid and glucose metabolism in humans. The proposed glucagon sensitivity test (comprising two elements 1) i.v. injection of 0.2 mg glucagon and 2) infusion of mixed amino acids 331 mg/hour/kg) is based on nine pilot studies which are presented. Calculation of a proposed glucagon sensitivity index with respect to amino acid catabolism is also described. Secondly, we describe a complete study protocol (GLUSENTIC) according to which the glucagon sensitivity test will be applied in a cross-sectional study currently taking place. 65 participants including 20 individuals with a BMI 18.6-25 kg/m2, 30 individuals with a BMI ≥ 25-40 kg/m2, and 15 individuals with type 1 diabetes with a BMI between 18.6 and 40 kg/m2 will be included. Participants will be grouped according to their degree of hepatic steatosis measured by whole-liver magnetic resonance imaging (MRI). The primary outcome measure will be differences in the glucagon sensitivity index between individuals with and without hepatic steatosis. Developing a glucagon sensitivity test and index may provide insight into the physiological and pathophysiological mechanism of glucagon action and glucagon-based therapies.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Glucagón / Enfermedad del Hígado Graso no Alcohólico Tipo de estudio: Diagnostic_studies / Guideline / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Peptides Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Glucagón / Enfermedad del Hígado Graso no Alcohólico Tipo de estudio: Diagnostic_studies / Guideline / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Peptides Año: 2023 Tipo del documento: Article