Intravenous Allopurinol to Improve Heart Function in Individuals With Dilated Cardiomyopathy

Allopurinol and Cardiac Function Pilot Study in Idiopathic Dilated Cardiomyopathy

This study will determine whether an acute infusion of intravenous allopurinol improves the inotropic response to dobutamine in patients with idiopathic dilated cardiomyopathy (DCM) as measured by cardiac magnetic resonance imaging (CMR).

Study Overview

• Status: Withdrawn
• Conditions: Heart Diseases; Cardiovascular Diseases; Cardiomyopathy, Dilated; Heart Failure, Congestive
• Intervention / Treatment: Drug: Allopurinol; Drug: Dobutamine

Detailed Description

BACKGROUND:

DCM is a poorly understood cause of systolic heart failure and is the most common indication for heart transplantation in the United States. Despite advances in medical and device therapy, the 5-year mortality of patients with DCM remains near 50%.

Oxidative stress, an imbalance between the formation and degradation of free radicals within the myocardium, contributes to metabolic derangements in patients with DCM. The enzyme xanthine oxidase (XO), a potent source of oxidative stress, is expressed in the failing heart, and it uncouples cardiac energy consumption from cardiac contraction in the setting of chronic heart failure. These effects can be reversed by inhibiting XO with the XO inhibitor allopurinol, resulting in a marked increase in cardiac efficiency. These findings provide a rationale for using allopurinol to enhance cardiac function in DCM. However, there is little data on the effects of allopurinol therapy on cardiac function. Therefore, the primary aim of this study is to determine whether an acute infusion of intravenous allopurinol improves the inotropic response to beta-adrenergic stimulation in patients with idiopathic DCM.

Decreased beta-adrenergic responsiveness is a characteristic feature of DCM that is attributable in part to decreased expression of the beta 1-receptor in chronic heart failure, as well as dysregulation of down-stream signaling pathways. Improvement in beta-adrenergic responsiveness is a useful surrogate marker for long-term improvement in cardiac structure, function, and decreased cardiac events. Traditionally, invasive hemodynamic monitoring using pressure and pressure/volume catheters has been the method of choice to quantify the inotropic response in heart failure. However, newly developed magnetic resonance imaging (MRI) techniques now allow precise assessment of the inotropic response non-invasively. Studies have shown that tagged CMR is a reproducible, noninvasive method to quantify the inotropic response to the beta 1 agonist dobutamine in individuals with structurally normal hearts. Specifically, radial strain (E1) and circumferential strain (E2) are measured at increasing doses of dobutamine using tagged CMR. Changes in these strain parameters, now referred to as delta E1 and delta E2, are precise measurements of the beta-inotropic response.

DESIGN NARRATIVE:

An estimated 20 patients with DCM will be randomized in a 1:1 ratio fashion to receive allopurinol or placebo. The primary aim of this investigation is to determine whether an acute infusion of intravenous allopurinol improves the inotropic response to dobutamine in patients with idiopathic DCM as measured by CMR. Specifically, the study will test the hypothesis that a single dose of intravenous allopurinol, compared to placebo, enhances delta E1 and delta E2. Secondary aims of this study are as follows: 1) to determine whether the response to allopurinol is associated with baseline XO activity and levels of natriuretic peptides (investigators predict that augmentation in delta E1 and delta E2 will correlate positively with baseline plasma uric acid and plasma B-type natriuretic peptide [BNP]); and 2) to demonstrate that tagged dobutamine CMR is a useful non-invasive technique to assess pharmacologic responses in patients with heart failure.

• Study Type: Interventional
• Phase: Phase 2; Phase 1

Contacts and Locations

Study Locations

• United States
  • Pennsylvania
    • Philadelphia, Pennsylvania, United States, 19104
      • University of Pennsylvania

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Diagnosis of idiopathic cardiomyopathy (defined by an ejection fraction less than or equal to 35% that has been assessed by any method within 6 months prior to study entry AND no evidence of coronary artery disease, as determined by coronary angiography or stress perfusion imaging within 2 years prior to study entry)
• New York Heart Association (NYHA) Class I - II heart failure
• Stable heart failure medication for at least 1 month prior to study entry
• Able to lie flat for 45 minutes

Exclusion Criteria:

• History of poorly controlled hypertension and concentric left ventricular hypertrophy on echocardiography suggesting hypertensive cardiomyopathy
• History of biopsy-proven myocarditis
• Peripartum cardiomyopathy
• Allopurinol therapy within the 6 months prior to study entry
• Allopurinol allergy
• Contraindication to allopurinol because of concomitant therapy with one of the following: azathioprine, cyclophosphamide, dicumarol, uricosuric agents (e.g., probenecid), ampicillin, amoxicillin, chlorpropamide, or cyclosporine
• Acute gout
• Estimated creatinine clearance less than 20 ml/min
• Total bilirubin greater than 2 times upper limit of normal
• Serum aspartate AST or alanine ALT greater than 3 times the upper limit of normal
• White blood cell count less than 2,000
• Platelet count less than 80,000
• Hemoglobin less than 8 mg/dl
• Use of intravenous inotropes
• History of untreated symptomatic ventricular tachycardia
• History of sustained ventricular tachycardia induced by dobutamine

• Contraindication to MRI because of one of the following:

  1. Starr-Edwards pre-6000 series prosthetic valves or prosthetic valves for which model can not be determined
  2. Implanted pacemaker
  3. Implanted cardioverter-defibrillator intracranial aneurysm clips
  4. Other implanted medical devices that are known to be MRI incompatible (e.g., cochlear implants and spinal stimulators)
  5. History of foundry-work that could create ocular metallic fragments
• Hospitalization at least 1 month prior to study entry

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Basic Science
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Quadruple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Placebo Comparator: placebo	Drug: Dobutamine
Experimental: allopurinol	Drug: Allopurinol; Drug: Dobutamine

What is the study measuring?

Primary Outcome Measures

Outcome Measure
radial and circumferential strain after infusion of allopurinol as measured by cardiac MRI (measured at Day 1)

Collaborators and Investigators

• Sponsor: University of Pennsylvania
• Collaborators: National Heart, Lung, and Blood Institute (NHLBI)
• Investigators: Study Chair: Thomas P. Cappola, University of Pennsylvania

Study record dates

Study Major Dates

• Study Start: June 1, 2003
• Primary Completion (Actual): June 1, 2013
• Study Completion (Actual): June 1, 2013

Study Registration Dates

• First Submitted: January 20, 2006
• First Submitted That Met QC Criteria: January 20, 2006
• First Posted (Estimate): January 24, 2006

Study Record Updates

• Last Update Posted (Estimate): June 19, 2013
• Last Update Submitted That Met QC Criteria: June 17, 2013
• Last Verified: June 1, 2013

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Genetic Diseases, Inborn; Cardiomegaly; Laminopathies; Heart Failure; Heart Diseases; Cardiovascular Diseases; Cardiomyopathies; Cardiomyopathy, Dilated; Physiological Effects of Drugs; Adrenergic Agents; Neurotransmitter Agents; Molecular Mechanisms of Pharmacological Action; Autonomic Agents; Peripheral Nervous System Agents; Enzyme Inhibitors; Antirheumatic Agents; Antimetabolites; Protective Agents; Adrenergic Agonists; Cardiotonic Agents; Antioxidants; Free Radical Scavengers; Gout Suppressants; Adrenergic beta-Agonists; Sympathomimetics; Adrenergic beta-1 Receptor Agonists; Allopurinol; Dobutamine
• Other Study ID Numbers: 353; K23HL071562 (U.S. NIH Grant/Contract)