This study tests the hypothesis that allopurinol, a xanthine oxidase inhibitor, improves heart metabolism in patients with heart failure.
Xanthine oxidase have been reported to improve mechano-energetic coupling in failing hearts. The investigators developed a means to directly measure creatine kinase flux, the major energy reserve of the heart, in the human heart exploiting new magnetic resonance technologies. The investigators propose to study 10 healthy subjects and up to 25 with heart failure (dilated cardiomyopathy) before and after a single 300mg IV infusion of allopurinol.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
18
intravenous infusion of allopurinol (300mg)
intravenous infusion of 50 ml dose of 5% dextrose
Johns Hopkins Hospital
Baltimore, Maryland, United States
Myocardial Creatine Kinase (CK) Flux Pre Intravenous Allopurinol Infusion
Magnetic resonance spectroscopy (MRS) Measurement of Myocardial CK Flux Pre Intravenous Allopurinol Infusion
Time frame: Onset of imaging acquisition.
Myocardial CK Flux Post Intravenous Allopurinol Infusion.
The mean rate of adenosine triphosphate (ATP) flux through the creatine kinase reaction in the heart.
Time frame: acute (within 15 minutes of single infusion)
Cardiac PCr/ATP Pre Intravenous Infusion
The mean ratio of creatine phosphate (PCr) to ATP in the heart. This measure, as a ratio, is unitless.
Time frame: Onset of image acquisition.
Cardiac PCr/ATP Post Intravenous Infusion
The mean ratio of creatine phosphate (PCr) to ATP in the heart. This measure, as a ratio, is unitless.
Time frame: acute (within 15 minutes of single infusion)
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