Effect of Uric Acid-Lowering Agents on Cardiovascular Outcome in Patients With Heart Failure: A Systematic Review and Meta-Analysis of Clinical Studies

Author:

Kanbay Mehmet1ORCID,Afsar Baris2,Siriopol Dimitrie3ORCID,Dincer Neris4,Erden Nihan4,Yilmaz Onur4,Sag Alan A.5,Kuwabara Masanari6,Cherney David78,Rossignol Patrick9,Ortiz Alberto10,Covic Adrian3

Affiliation:

1. Department of Medicine, Division of Nephrology, Koc University School of Medicine, Istanbul, Turkey

2. Division of Nephrology, Department of Internal Medicine, Suleyman Demirel University School of Medicine, Isparta Turkey

3. Nephrology Clinic, Dialysis and Renal Transplant Center, ‘C.I. PARHON’ University Hospital, ‘Grigore T. Popa’ University of Medicine, Iasi, Romania

4. Department of Medicine, Koc University School of Medicine, Istanbul, Turkey

5. Division of Vascular and Interventional Radiology, Department of Radiology, Duke University Medical Center, Durham, NC, USA

6. Department of Cardiology, Toranomon Hospital, Tokyo, Japan

7. Toronto General Hospital Research Institute, UHN, Toronto, Canada

8. Departments of Physiology and Pharmacology and Toxicology, University of Toronto, Ontario, Canada

9. Université de Lorraine, INSERM CIC-P 1433, CHRU de Nancy, INSERM U1116, FCRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists), Nancy, France

10. Dialysis Unit, School of Medicine, IIS-Fundacion Jimenez Diaz, Universidad Autónoma de Madrid, Madrid, Spain

Abstract

Several trials have been completed in patients with heart failure (HF) treated with uric acid (UA)-lowering agents with inconsistent results. We aimed to investigate whether lowering UA would have an effect on mortality and cardiovascular (CV) events in patients with HF in a systematic review and meta-analysis. The primary outcome measures were all-cause mortality, CV mortality, CV events, and CV hospitalization in patients with HF. We included 11 studies in our final analysis. Overall, allopurinol treatment was associated with a significant increase in the risk for all-cause mortality (hazard ratio [HR]: 1.24, 95% confidence interval [CI]: 1.04-1.49, P = .02). The trial heterogeneity is high (heterogeneity χ2 = 37.3, I2 = 73%, P < .001). With regard to CV mortality, allopurinol treatment was associated with a 42% increased risk of CV mortality (HR: 1.42, 95% CI: 1.11-1.81, P = .005). There was a trend toward increased CV hospitalization in the same group (HR: 1.21, 95% CI: 0.95-1.53, P = .12). Uric acid-lowering treatments increase all-cause and CV mortality but did not increase CV hospitalization significantly in this study.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine

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