Excellent blood sugar control by liraglutide in diabetics on beta-blockers
The glucagon-like peptide-1 (GLP-1) agonist drug, liraglutide, seems to
provide excellent blood sugar control in patients with type 2 diabetes who are
also taking a beta-blocker, specifically propranolol, to prevent bleeding from
esophageal varices due to cirrhosis, but it seems to hamper the pharmacological
effects of beta-blockers.
A case report has been published
in Annals of Internal Medicine.
Cirrhosis is the leading cause of portal hypertension with an increased
risk of developing esophageal varices.Beta-blockers are used to lower portal
pressure and decrease the risk of bleeding from esophageal varices and decrease
mortality.
When using beta-blockers to prevent bleeding from esophageal varices,
clinicians use the resting heart rate as a guide, as these therapies lower
heart rate. GLP-1s are used to treat diabetes because they lower blood sugar
levels and are especially useful when the patient is obese and has nonalcoholic
fatty liver disease, but they are known to increase heart rate, although not significantly.
No data are available on the concomitant treatment with GLP-1 analogues and
β-blockers in patients with cirrhosis and diabetes.
Researchers from University of Bologna, Policlinico Sant'Orsola-Malpighi, Bologna, Italy studied 18 consecutive patients with cirrhosis who were receiving propranolol to prevent variceal bleeding while also receiving liraglutide for uncontrolled type 2 diabetes. Liraglutide provided optimal control of blood sugar, HbA1c and body weight, but the researchers observed a lack of optimal effect of beta-blockers on heart rate after starting a GLP-1 receptor agonist. However, in this small cohort no increase in bleeding rate was observed. The researchers propose a mechanistic molecular explanation of how a GLP-1 receptor agonist might prevent beta-adrenergic receptor blockade.
Researchers from University of Bologna, Policlinico Sant'Orsola-Malpighi, Bologna, Italy studied 18 consecutive patients with cirrhosis who were receiving propranolol to prevent variceal bleeding while also receiving liraglutide for uncontrolled type 2 diabetes. Liraglutide provided optimal control of blood sugar, HbA1c and body weight, but the researchers observed a lack of optimal effect of beta-blockers on heart rate after starting a GLP-1 receptor agonist. However, in this small cohort no increase in bleeding rate was observed. The researchers propose a mechanistic molecular explanation of how a GLP-1 receptor agonist might prevent beta-adrenergic receptor blockade.
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