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Combination GLP-1 and Insulin Treatment Fails to Alter Myocardial Fuel Selection vs. Insulin Alone in Type 2 Diabetes.

Citation
Mather, K. J., et al. “Combination Glp-1 And Insulin Treatment Fails To Alter Myocardial Fuel Selection Vs. Insulin Alone In Type 2 Diabetes.”. The Journal Of Clinical Endocrinology And Metabolism, pp. 3456-3465.
Center Indiana University
Author Kieren J Mather, Robert Considine V, LaTonya Hamilton, Niral A Patel, Carla Mathias, Wendy Territo, Adam G Goodwill, Johnathan D Tune, Mark A Green, Gary D Hutchins
Abstract

Context: It is unclear if effects of glucagon-like peptide-1 (GLP-1) and clinically available GLP-1 agonists on the heart occur at clinical doses in humans, possibly contributing to reduced cardiovascular disease risk.

Objective: To determine whether liraglutide, at clinical dosing, augments myocardial glucose uptake (MGU) alone or combined with insulin compared with insulin alone in metformin-treated type 2 diabetes mellitus (T2D).

Design: In a randomized clinical trial of patients with T2D treated with metformin plus oral agents or basal insulin, myocardial fuel use was compared after 3 months of treatment with insulin detemir, liraglutide, or combination detemir plus liraglutide added to background metformin.

Main Outcome Measures: Myocardial blood flow (MBF), fuel selection, and rates of fuel use were evaluated using positron emission tomography, powered to demonstrate large effects.

Results: MBF was greater in the insulin-treated groups [median (25th, 75th percentile): detemir, 0.64 mL/g/min (0.50, 0.69); liraglutide, 0.52 mL/g/min (0.46, 0.58); detemir plus liraglutide, 0.75 mL/g/min (0.55, 0.77); P = 0.035 comparing three groups, P = 0.01 comparing detemir groups to liraglutide alone]. There were no evident differences among groups in MGU [detemir, 0.040 µmol/g/min (0.013, 0.049); liraglutide, 0.055 µmol/g/min (0.019, 0.105); detemir plus liraglutide, 0.037 µmol/g/min (0.009, 0.046); P = 0.68 comparing three groups]. There were no treatment-group differences in measures of myocardial fatty acid uptake or handling, and no differences in total oxidation rate.

Conclusion: These observations argue against large effects of GLP-1 agonists on myocardial fuel metabolism as mediators of beneficial treatment effects on myocardial function and ischemia protection.

Year of Publication
2018
Journal
The Journal of clinical endocrinology and metabolism
Volume
103
Issue
9
Number of Pages
3456-3465
Date Published
12/2018
ISSN Number
1945-7197
DOI
10.1210/jc.2018-00712
Alternate Journal
J. Clin. Endocrinol. Metab.
PMID
30020461
PMCID
PMC6126889
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