Key result
Low-dose adenosine infusion significantly increased peak systolic velocity in ischemic left ventricular walls during maximal exercise compared to placebo, indicating an ischemic preconditioning effect.
Why the study?
Does intravenous low-dose adenosine reduce ischemic burden and improve regional left ventricular systolic function in patients with severe coronary artery disease?
RCT (n=9)
Double-blind
Randomized cross-over
No
Does intravenous low-dose adenosine reduce ischemic burden and improve regional left ventricular systolic function in patients with severe coronary artery disease?
Low-dose adenosine infusion prior to exercise reduces ischemic burden and improves regional left ventricular systolic function in patients with severe coronary artery disease, demonstrating a preconditioning effect.
Answers are grounded in this paper and cite their sources.
May support low-dose adenosine preconditioning before exercise in severe CAD; confirms ischemic preconditioning in RCT.
INTRODUCTION: In vivo and in vitro evidence suggests that adenosine and its agonists play key roles in the process of ischemic preconditioning. The effects of low-dose adenosine infusion on ischemic preconditioning have not been thoroughly studied in humans. AIMS: We hypothesised that a low-dose adenosine infusion could reduce the ischemic burden evoked by physical exercise and improve the regional left ventricular (LV) systolic function. MATERIALS AND METHODS: We studied nine severely symptomatic male patients with severe coronary artery disease. Myocardial ischemia was induced by exercise on two separate occasions and quantified by Tissue Doppler Echocardiography. Prior to the exercise test, intravenous low-dose adenosine or placebo was infused over ten minutes according to a randomized, double blind, cross-over protocol. The LV walls were defined as ischemic if a reduction, no increment, or an increment of < 15% in peak systolic velocity (PSV) was observed during maximal exercise compared to the baseline values observed prior to placebo-infusion. Otherwise, the LV walls were defined as non-ischemic. RESULTS: PSV increased from baseline to maximal exercise in non-ischemic walls both during placebo (P = 0.0001) and low-dose adenosine infusion (P = 0.0009). However, in the ischemic walls, PSV increased only during low-dose adenosine infusion (P = 0.001), while no changes in PSV occurred during placebo infusion (P = NS). CONCLUSION: Low-dose adenosine infusion reduced the ischemic burden and improved LV regional systolic function in the ischemic walls of patients with exercise-induced myocardial ischemia, confirming that adenosine is a potential preconditioning agent in humans.
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Sadigh et al. (2009) conducted an RCT in Severe coronary artery disease (n=9). Adenosine vs. Placebo (saline) was evaluated on Peak systolic velocity (PSV) in ischemic left ventricular walls during maximal exercise (p=<0.01). Low-dose adenosine infusion significantly increased peak systolic velocity in ischemic left ventricular walls during maximal exercise compared to placebo, indicating an ischemic preconditioning effect.
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