Journal of Cardiac Failure
Volume 16, Issue 3 , Pages 260-267, March 2010

The Effect of Renin-Angiotensin System Inhibitors on Mortality and Heart Failure Hospitalization in Patients With Heart Failure and Preserved Ejection Fraction: A Systematic Review and Meta-Analysis

  • Ravi V. Shah, MD

      Affiliations

    • Cardiology Division, Department of Medicine, Massachusetts General Hospital, Boston, MA
    • Harvard Medical School, Boston, MA
  • ,
  • Akshay S. Desai, MD, MPH

      Affiliations

    • Cardiovascular Division, Brigham and Women's Hospital, Boston, MA
    • Harvard Medical School, Boston, MA
  • ,
  • Michael M. Givertz, MD

      Affiliations

    • Cardiovascular Division, Brigham and Women's Hospital, Boston, MA
    • Harvard Medical School, Boston, MA
    • Corresponding Author InformationReprint requests: Michael M. Givertz, MD, Cardiovascular Division, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115. Tel: 617-732-7367; Fax: 617-264-5265.

Received 30 July 2009; received in revised form 25 November 2009; accepted 30 November 2009. published online 06 January 2010.

Abstract 

Background

Although renin-angiotensin system (RAS) inhibitors have little demonstrable effect on mortality in patients with heart failure and preserved ejection fraction (HF-PEF), some trials have suggested a benefit with regard to reduction in HF hospitalization.

Methods and Results

Here, we systematically review and evaluate prospective clinical studies of RAS inhibitors enrolling patients with HF-PEF, including the 3 major trials of RAS inhibition (Candesartan in Patients with Chronic Heart Failure and Preserved Left Ventricular Ejection Fraction [CHARM-Preserved], Irbesartan in Patients with Heart Failure and Preserved Ejection Fraction [I-PRESERVE], and Perindopril in Elderly People with Chronic Heart Failure [PEP-CHF]). We also conducted a pooled analysis of 8021 patients in the 3 major randomized trials of RAS inhibition in HF-PEF (CHARM-Preserved, I-PRESERVE, and PEP-CHF) in fixed-effect models, finding no clear benefit with regard to all-cause mortality (odds ratio [OR] 1.03, 95% confidence interval [CI], 0.92-1.15; P=.62), or HF hospitalization (OR 0.90, 95% CI 0.80-1.02; P=.09).

Conclusions

Although RAS inhibition may be valuable in the management of comorbidities related to HF-PEF, RAS inhibition in HF-PEF is not associated with consistent reduction in HF hospitalization or mortality in this emerging cohort.

Key Words: Heart failure, meta-analysis, drugs, renin-angiotensin system

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 R.V.S. has received fellowship support from the National Institutes of Health, National Heart, Lung and Blood Institute Heart Failure Clinical Research Network (U01 HL084904).

PII: S1071-9164(09)01194-4

doi:10.1016/j.cardfail.2009.11.007

Journal of Cardiac Failure
Volume 16, Issue 3 , Pages 260-267, March 2010