Abstract

BackgroundImpaired coronary microcirculation is associated with a poor prognosis in patients with type 2 diabetes. In the absence of stenosis of major coronary arteries, coronary flow reserve (CFR) reflects coronary microcirculation. Studies have shown beneficial effects of glucagon-like peptide-1 (GLP-1) on the cardiovascular system. The aim of the study was to explore the short-term effect of GLP-1 treatment on coronary microcirculation estimated by CFR in patients with type 2 diabetes.MethodsPatients with type 2 diabetes and no history of coronary artery disease were treated with either the GLP-1 analogue liraglutide or received no treatment for 10 weeks, in a randomized, single-blinded, cross-over setup with a 2 weeks wash-out period. The effect of liraglutide on coronary microcirculation was evaluated using non-invasive trans-thoracic Doppler-flow echocardiography during dipyridamole induced stress. Peripheral microvascular endothelial function was assessed by Endo-PAT2000®. Interventions were compared by two-sample t-test after ensuring no carry over effect.ResultsA total of 24 patients were included. Twenty patients completed the study (15 male; mean age 57 ± 9; mean BMI 33.1 ± 4.4, mean baseline CFR 2.35 ± 0.45). There was a small increase in CFR following liraglutide treatment (change 0.18, CI95% [-0.01; 0.36], p = 0.06) but no difference in effect in comparison with no treatment (difference between treatment allocation 0.16, CI95% [-0.08; 0.40], p = 0.18). Liraglutide significantly reduced glycated haemoglobin (HbA1c) (-10.1 mmol/mol CI95% [-13.9; -6.4], p = 0.01), systolic blood pressure (-10 mmHg CI95% [-17; -3], p = 0.01) and weight (-1.9 kg CI95% [-3.6; -0.2], p = 0.03) compared to no treatment. There was no effect on peripheral microvascular endothelial function after either intervention.ConclusionsIn this short-term treatment study, 10 weeks of liraglutide treatment had no significant effect on neither coronary nor peripheral microvascular function in patients with type 2 diabetes. Further long-term studies, preferably in patients with more impaired microvascular function and using a higher dosage of GLP-1 analogues, are needed to confirm these findings.Trial registrationClinicalTrials.gov: NCT01931982.Electronic supplementary materialThe online version of this article (doi:10.1186/s12933-015-0206-3) contains supplementary material, which is available to authorized users.

Highlights

  • Patients with type 2 diabetes often suffer from both macro- and microvascular disease with cardiovascular disease being the most important contributor to mortality

  • Study population We assessed 621 patients who were followed for type 2 diabetes in outpatient clinics for eligibility (Figure 3). 213 patients were excluded due to co-morbidity, primarily previous coronary artery disease (CAD) (37%, including AMI, PCI and CABG), reduced renal function (13%) and gastrointestinal disease (12%, including inflammatory bowel disease, previous pancreatitis and gastric bypass)

  • The main reason for reluctance to participating in the study was the concern for potential side-effects to the test drug liraglutide (Victoza®)

Read more

Summary

Introduction

Patients with type 2 diabetes often suffer from both macro- and microvascular disease with cardiovascular disease being the most important contributor to mortality. Myocardial microvascular dysfunction is caused by reduced vasodilator reserve of the small coronary arteries. Reduced CFR has been proven a strong predictor of poor prognosis in patients with suspected coronary artery disease (CAD) [3,4,5]. Studies have shown CFR to provide independent prognostic information on patients with type 2 diabetes and no history of CAD. Impaired coronary microcirculation is associated with a poor prognosis in patients with type 2 diabetes. Studies have shown beneficial effects of glucagon-like peptide-1 (GLP-1) on the cardiovascular system. The aim of the study was to explore the short-term effect of GLP-1 treatment on coronary microcirculation estimated by CFR in patients with type 2 diabetes

Objectives
Methods
Results
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call