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Acute effects on glucose tolerance by neprilysin inhibition in patients with type 2 diabetes.
Wewer Albrechtsen, Nicolai J; Møller, Andreas; Martinussen, Christoffer; Gluud, Lise L; Rashu, Elias B; Richter, Michael M; Plomgaard, Peter; Goetze, Jens P; Kjeldsen, Sasha; Hansen, Lasse Holst; Gustafsson, Finn; Deacon, Carolyn F; Holst, Jens J; Madsbad, Sten; Bojsen-Møller, Kirstine N.
Afiliação
  • Wewer Albrechtsen NJ; Department of Clinical Biochemistry, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Møller A; Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Martinussen C; NNF Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Gluud LL; Department of Clinical Biochemistry, Bispebjerg and Frederiksberg Hospital, University of Copenhagen, Copenhagen, Denmark.
  • Rashu EB; Department of Endocrinology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
  • Richter MM; Department of Endocrinology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
  • Plomgaard P; Gastrounit, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
  • Goetze JP; Gastrounit, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark.
  • Kjeldsen S; Department of Clinical Biochemistry, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Hansen LH; Department of Clinical Biochemistry, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Gustafsson F; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Deacon CF; Department of Clinical Biochemistry, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Holst JJ; Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Madsbad S; Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Bojsen-Møller KN; NNF Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Diabetes Obes Metab ; 24(10): 2017-2026, 2022 10.
Article em En | MEDLINE | ID: mdl-35676803
AIMS: Sacubitril/valsartan is a neprilysin-inhibitor/angiotensin II receptor blocker used for the treatment of heart failure. Recently, a post-hoc analysis of a 3-year randomized controlled trial showed improved glycaemic control with sacubitril/valsartan in patients with heart failure and type 2 diabetes. We previously reported that sacubitril/valsartan combined with a dipeptidyl peptidase-4 inhibitor increases active glucagon-like peptide-1 (GLP-1) in healthy individuals. We now hypothesized that administration of sacubitril/valsartan with or without a dipeptidyl peptidase-4 inhibitor would lower postprandial glucose concentrations (primary outcome) in patients with type 2 diabetes via increased active GLP-1. METHODS: We performed a crossover trial in 12 patients with obesity and type 2 diabetes. A mixed meal was ingested following five respective interventions: (a) a single dose of sacubitril/valsartan; (b) sitagliptin; (c) sacubitril/valsartan + sitagliptin; (d) control (no treatment); and (e) valsartan alone. Glucose, gut and pancreatic hormone responses were measured. RESULTS: Postprandial plasma glucose increased by 57% (incremental area under the curve 0-240 min) (p = .0003) and increased peak plasma glucose by 1.7 mM (95% CI: 0.6-2.9) (p = .003) after sacubitril/valsartan compared with control, whereas postprandial glucose levels did not change significantly after sacubitril/valsartan + sitagliptin. Glucagon, GLP-1 and C-peptide concentrations increased after sacubitril/valsartan, but insulin and glucose-dependent insulinotropic polypeptide did not change. CONCLUSIONS: The glucose-lowering effects of long-term sacubitril/valsartan treatment reported in patients with heart failure and type 2 diabetes may not depend on changes in entero-pancreatic hormones. Neprilysin inhibition results in hyperglucagonaemia and this may explain the worsen glucose tolerance observed in this study. CLINICALTRIALS: gov (NCT03893526).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos de Bifenilo / Glicemia / Neprilisina / Diabetes Mellitus Tipo 2 / Antagonistas de Receptores de Angiotensina / Valsartana / Aminobutiratos / Insuficiência Cardíaca / Hipoglicemiantes Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Aged / Humans / Male / Middle aged Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos de Bifenilo / Glicemia / Neprilisina / Diabetes Mellitus Tipo 2 / Antagonistas de Receptores de Angiotensina / Valsartana / Aminobutiratos / Insuficiência Cardíaca / Hipoglicemiantes Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Aged / Humans / Male / Middle aged Idioma: En Ano de publicação: 2022 Tipo de documento: Article