HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

The APEX trial: Effects of allopurinol on exercise capacity, coronary and peripheral endothelial function, and natriuretic peptides in patients with cardiac syndrome X.

Abstract
The role of endothelial dysfunction and oxidative stress in the pathogenesis of cardiac syndrome X has recently been recognized. Allopurinol has previously been shown to improve endothelial dysfunction, reduce oxidative stress burden, and improve myocardial efficiency. In this "proof of concept" study, we investigated the effect of allopurinol on exercise capacity, coronary and peripheral endothelial function, and serum B-type natriuretic peptide (BNP: a marker of cardiac function and myocardial ischemia) in patients with cardiac syndrome X.
METHODS AND RESULTS:
This study was a randomized, double-blind, placebo-control crossover trial. Nineteen patients (mean age 59 ± 10 years, 11 women and 8 men) with cardiac syndrome X were randomized to a 6-week treatment with either allopurinol (600 mg/day) or placebo. After 4 weeks of washout period, they were crossed over to the other arm. Outcomes measured at baseline and after treatment were maximum exercise time (ET) derived from Bruce protocol exercise treadmill test, serum BNP measurement, coronary flow reserve (CFR) as assessed by measuring the response of flow velocity in the left anterior descending artery to adenosine, and flow-mediated vasodilatation of the brachial artery (FMD). Allopurinol significantly reduced serum uric acid levels when compared with placebo (-48 ± 24% vs 1.9 ± 11%, P < .001). There was no significant difference in maximum ET, CFR, and FMD between allopurinol and placebo. However, there was a trend that allopurinol reduced serum BNP when compared to placebo (-8% [interquartile range -22% to 65%] vs 44% [interquartile range -18% to 140%]; P = .07).
CONCLUSION:
In patients with cardiac syndrome X, high-dose allopurinol did not improve exercise capacity, and coronary or peripheral endothelial function.
AuthorsTiong Keng Lim, Awson Noman, Anna Maria J Choy, Faisel Khan, Allan D Struthers, Chim C Lang
JournalCardiovascular therapeutics (Cardiovasc Ther) Vol. 36 Issue 1 (Feb 2018) ISSN: 1755-5922 [Electronic] England
PMID29080386 (Publication Type: Journal Article, Randomized Controlled Trial)
Copyright© 2017 John Wiley & Sons Ltd.
Chemical References
  • Antioxidants
  • Biomarkers
  • Natriuretic Peptide, Brain
  • Allopurinol
Topics
  • Aged
  • Allopurinol (adverse effects, therapeutic use)
  • Antioxidants (adverse effects, therapeutic use)
  • Biomarkers (blood)
  • Blood Flow Velocity
  • Brachial Artery (drug effects, metabolism, physiopathology)
  • Coronary Circulation (drug effects)
  • Coronary Vessels (drug effects, metabolism, physiopathology)
  • Cross-Over Studies
  • Double-Blind Method
  • Endothelium, Vascular (drug effects, metabolism, physiopathology)
  • Exercise Tolerance (drug effects)
  • Female
  • Humans
  • Male
  • Microvascular Angina (blood, diagnosis, drug therapy, physiopathology)
  • Middle Aged
  • Natriuretic Peptide, Brain (blood)
  • Oxidative Stress (drug effects)
  • Recovery of Function
  • Scotland
  • Time Factors
  • Treatment Outcome
  • Vasodilation (drug effects)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: