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Glucagon resistance in individuals with obesity and hepatic steatosis can be measured using the GLUSENTIC test and index.
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; Andersen, Thomas L; Johannesen, Helle H; Trammell, Samuel A J; Grevengoed, Trisha J; Madsbad, Sten; Vilstrup, Hendrik; Vinholt Schiødt, Frank; Møller, Andreas; Rashu, Elias B; Nørgaard, Kirsten; Schmidt, Signe; Gluud, Lise L; Haugaard, Steen B; Holst, Jens J; Rungby, Jørgen; Wewer Albrechtsen, Nicolai J.
Afiliación
  • Kjeldsen SAS; Department of Clinical Biochemistry, Copenhagen University Hospital Bispebjerg, Copenhagen, Denmark.
  • Richter MM; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Jensen NJ; Department of Clinical Biochemistry, Copenhagen University Hospital Bispebjerg, Copenhagen, Denmark.
  • Nilsson MSD; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Heinz N; Department of Endocrinology, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Nybing JD; Department of Endocrinology, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Linden FH; Department of Clinical Biochemistry, Copenhagen University Hospital Bispebjerg, Copenhagen, Denmark.
  • Høgh-Schmidt E; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Boesen MP; Department of Radiology, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Andersen TL; Department of Radiology, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Johannesen HH; Department of Radiology, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Trammell SAJ; Department of Radiology, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Grevengoed TJ; Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet, Copenhagen, Denmark.
  • Madsbad S; Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet, Copenhagen, Denmark.
  • Vilstrup H; Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Vinholt Schiødt F; Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Møller A; Department of Endocrinology, Hvidovre University Hospital, Hvidovre, Denmark.
  • Rashu EB; Department of Hepatology and Gastroenterology, Aarhus University Hospital, Aarhus, Denmark.
  • Nørgaard K; Department of Clinical Medicine, Bispebjerg University Hospital, Copenhagen, Denmark.
  • Schmidt S; Gastro unit, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
  • Gluud LL; Gastro unit, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
  • Haugaard SB; Steno Diabetes Center Copenhagen, Herlev, Denmark.
  • Holst JJ; Steno Diabetes Center Copenhagen, Herlev, Denmark.
  • Rungby J; Gastro unit, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
  • Wewer Albrechtsen NJ; Department of Endocrinology, Bispebjerg University Hospital, Copenhagen, Denmark.
Diabetes ; 2024 Jul 08.
Article en En | MEDLINE | ID: mdl-38976454
ABSTRACT
Increased plasma levels of glucagon (hyperglucagonaemia) promote diabetes development but is also observed in patients with metabolic dysfunction-associated steatotic liver disease (MASLD). This may reflect hepatic glucagon resistance towards amino acid catabolism. A clinical test for measuring glucagon resistance has not been validated. We evaluated our glucagon sensitivity (GLUSENTIC) test, consisting of two study days a glucagon injection and measurements of plasma amino acids, and an infusion of mixed amino acids and subsequent calculation of the GLUSENTIC index (primary outcome measure) from measurements of glucagon and amino acids. To distinguish glucagon-dependent from insulin-dependent actions on amino acid metabolism, we also studied patients with type 1 diabetes (T1D). The delta-decline in total amino acids was 49% lower in MASLD following exogenous glucagon (p=0.01), and the calculated GLUSENTIC index was 34% lower in MASLD (p<0.0001), but not T1D (p>0.99). In contrast, glucagon-induced glucose increments were similar in controls and MASLD (p=0.41). The GLUSENTIC test and index may be used to measure glucagon resistance in individuals with obesity and MASLD.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Diabetes Año: 2024 Tipo del documento: Article País de afiliación: Dinamarca

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Diabetes Año: 2024 Tipo del documento: Article País de afiliación: Dinamarca