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Hemodynamic Effects of Glucagon - A Literature Review

Kasper Meidahl Petersen, Søren Bøgevig, Jens Juul Holst, Filip Krag Knop, Mikkel Bring Christensen

53 Citations (Scopus)

Abstract

Context: Glucagon's effects on hemodynamic parameters - most notably heart rate and cardiac contractility - are overlooked. The glucagon receptor is a central target in novel and anticipated type 2 diabetes therapies and hemodynamic consequences of glucagon signaling have therefore become increasingly important. In this review we summarize and evaluate published studies on glucagon pharmacology with focus on clinical hemodynamic effects in humans.

Evidence acquisition: PubMed, EMBASE and the Cochrane library were searched for clinical studies concerning hemodynamic effects of glucagon (no year restriction). Papers reporting effects of a defined glucagon dose on any hemodynamic parameter were included. Reference searches were conducted in retrieved articles.

Evidence synthesis: Hemodynamic effects of glucagon have been investigated mainly in cohort-studies of heart failure patients receiving large glucagon bolus injections. The identified studies had shortcomings related to restricted patient groups, lack of a control group, randomization or blinding. We identified no properly conducted randomized clinical trials. The majority of human studies report stimulating effects of pharmacological glucagon doses on heart rate, cardiac contractility and blood pressure. The effects were characterized by short duration, inter-individual variation and rapid desensitization. Some studies reported no measurable effects of glucagon.

Conclusions: The level of evidence regarding hemodynamic effects of glucagon is low and observations in published studies are inconsistent. Actual effects, inter-individual variation, dose-response relationships and possible long-term effects of supra-physiological glucagon levels warrant further investigation.

Original languageEnglish
JournalThe Journal of clinical endocrinology and metabolism
Volume103
Issue number5
Pages (from-to)1804-1812
Number of pages8
ISSN0021-972X
DOIs
Publication statusPublished - 1 May 2018

Keywords

  • Journal Article

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