Abstract

BackgroundEnhancement of myocardial glucose uptake may reduce fatty acid oxidation and improve tolerance to ischemia. Hyperglycemia, in association with hyperinsulinemia, stimulates this metabolic change but may have deleterious effects on left ventricular (LV) function. The incretin hormone, glucagon-like peptide-1 (GLP-1), also has favorable cardiovascular effects, and has emerged as an alternative method of altering myocardial substrate utilization. In patients with coronary artery disease (CAD), we investigated: (1) the effect of a hyperinsulinemic hyperglycemic clamp (HHC) on myocardial performance during dobutamine stress echocardiography (DSE), and (2) whether an infusion of GLP-1(7-36) at the time of HHC protects against ischemic LV dysfunction during DSE in patients with type 2 diabetes mellitus (T2DM).MethodsIn study 1, twelve patients underwent two DSEs with tissue Doppler imaging (TDI)—one during the steady-state phase of a HHC. In study 2, ten patients with T2DM underwent two DSEs with TDI during the steady-state phase of a HHC. GLP-1(7-36) was infused intravenously at 1.2 pmol/kg/min during one of the scans. In both studies, global LV function was assessed by ejection fraction and mitral annular systolic velocity, and regional wall LV function was assessed using peak systolic velocity, strain and strain rate from 12 paired non-apical segments.ResultsIn study 1, the HHC (compared with control) increased glucose (13.0 ± 1.9 versus 4.8 ± 0.5 mmol/l, p < 0.0001) and insulin (1,212 ± 514 versus 114 ± 47 pmol/l, p = 0.01) concentrations, and reduced FFA levels (249 ± 175 versus 1,001 ± 333 μmol/l, p < 0.0001), but had no net effect on either global or regional LV function. In study 2, GLP-1 enhanced both global (ejection fraction, 77.5 ± 5.0 versus 71.3 ± 4.3%, p = 0.004) and regional (peak systolic strain −18.1 ± 6.6 versus −15.5 ± 5.4%, p < 0.0001) myocardial performance at peak stress and at 30 min recovery. These effects were predominantly driven by a reduction in contractile dysfunction in regions subject to demand ischemia.ConclusionsIn patients with CAD, hyperinsulinemic hyperglycemia has a neutral effect on LV function during DSE. However, GLP-1 at the time of hyperglycemia improves myocardial tolerance to demand ischemia in patients with T2DM.Trial Registration: http://www.isrctn.org. Unique identifier ISRCTN69686930

Highlights

  • Enhancement of myocardial glucose uptake may reduce fatty acid oxidation and improve tolerance to ischemia

  • It has a number of direct detrimental effects on the ischemic myocardium [2], hyperglycemia is representative of an acute metabolic stress characterised by high adrenergic-mediated levels of free fatty acids (FFA), insulin resistance and impaired glucose utilization [3]

  • Glucose concentrations at the steady state stage of the clamp were significantly higher than at baseline in the control study (13.3 ± 1.7 [hyperinsulinemic hyperglycemic clamp (HHC)] versus 4.9 ± 0.6 mmol/l [control], p < 0.0001). This was associated with elevated insulin (378 ± 174 [HHC] versus 86 ± 76 pmol/l [control], p = 0.0007) and reduced FFA concentrations (77 ± 74 [HHC] versus 429 ± 226umol/l [control], p = 0.0003)

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Summary

Introduction

Enhancement of myocardial glucose uptake may reduce fatty acid oxidation and improve tolerance to ischemia. Hyperglycemia is common in patients presenting with acute coronary syndromes (ACS) and a powerful predictor of morbidity and mortality [1] It has a number of direct detrimental effects on the ischemic myocardium [2], hyperglycemia is representative of an acute metabolic stress characterised by high adrenergic-mediated levels of free fatty acids (FFA), insulin resistance and impaired glucose utilization [3]. Attempts to modulate these metabolic derangements with insulinbased strategies have failed to demonstrate consistent clinical benefits [4, 5] and are yet to be established in the management of patients with ACS [6, 7]. GLP-1 appears attractive as a potential therapeutic adjunct for metabolic manipulation in patients with ischaemic heart disease (IHD)

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