Abstract

D-Ribose, a pentose sugar, has shown to improve myocardial high-energy phosphate stores depleted by ischemia. This study investigated the ability of D-Ribose with low dose dobutamine to improve the contractile response of viable myocardium to dobutamine and to assess the efficacy of D-ribose in reducing stress-induced ischemia. Twenty-six patients with ischemic cardiomyopathy completed a two-day, randomized, double blind crossover trial comparing the effects of D-Ribose and placebo on regional wall motion. On the first study day, either D-Ribose or placebo was infused for 4.5 hours. Low (5 and 10 μ/kg/min) and subsequently, high (up to 50 μ/kg/min) dose dobutamine echocardiography was then performed. On the second study day, patients crossed over to the alternative article for a similar 4.5 hours infusion time period and underwent a similar evaluation. The wall motion response during low dose dobutamine was the same with D-Ribose and placebo in 77% of segments (203/263, Kappa = 0.37). In segments with discordant responses, more segments improved with D-Ribose than with placebo (41 vs. 19 segments, p = 0.006). With high dose dobutamine infusion, the wall motion response (ischemia vs. no ischemia) was the same with D-Ribose and placebo in 83% of interpretable segments (301/363, kappa = 0.244). In segments with discordant responses, there were more ischemic segments with placebo compared to D-Ribose (36 vs. 26, p = 0.253). Nineteen patients developed ischemia during the dobutamine and placebo infusion and 13 patients had ischemia during dobutamine and D-ribose infusion (p = 0.109). D-Ribose improved contractile responses to dobutamine in viable myocardium with resting dysfunction but had no significant effect in reducing the frequency of stress-induced wall motion abnormalities.

Highlights

  • The maintenance of cellular integrity and contractility rely on adequate levels of adenosine triphosphate (ATP)

  • In the 62 myocardial segments with discordant results, there was no significant difference in the number of ischemic segments with placebo vs DR infusion (36 vs 26 segments, respectively, p = 0.253). This pilot study revealed that intravenous DR improved the contractile response of segments with resting dysfunction to low dose dobutamine infusion

  • DR improved the contractile response to dobutmaine in myocardial segments with resting dysfunction

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Summary

Introduction

The maintenance of cellular integrity and contractility rely on adequate levels of adenosine triphosphate (ATP). Myocardial ischemia alters oxidative metabolism resulting in lower tissue ATP levels along with an associated impairment in contractile function [1,2]. The repletion of ATP stores depends on the availability of the precursor phosphoribosyl-pyrophosphate (PRPP). Cardiovascular Ultrasound 2009, 7:5 http://www.cardiovascularultrasound.com/content/7/1/5 pentose monosaccharide, has been shown to accelerate ATP repletion in the ischemic myocardium by promoting the production of PRPP. DR enhanced the repletion of ATP after global and regional ischemia, resulting in an improvement in contractile function [3,4,5,6,7]. The effect of DR in ischemic contractile dysfunction in patients is unknown

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