Journal of the American Society of Hypertension
Volume 3, Issue 1 , Pages 52-68, January 2009

Diastolic dysfunction and heart failure with preserved ejection fraction: rationale for RAAS antagonist/CCB combination therapy

  • Krishna K. Gaddam, MD

      Affiliations

    • Corresponding Author InformationCorresponding author: Krishna K. Gaddam, MD, 115 Community Health Services Building, 933 19th Street South, Birmingham, Alabama 35294. Tel: 205-934-9281; fax: 205-934-1302
  • ,
  • Suzanne Oparil, MD

Vascular Biology and Hypertension Program, University of Alabama at Birmingham, Birmingham, Alabama, USA

Received 3 December 2007; accepted 28 June 2008. published online 15 September 2008.

Abstract 

A large number of patients who present with signs or symptoms of heart failure (HF) do not have evidence of left ventricular systolic dysfunction. As a result, HF in the presence of normal or preserved ejection fraction, or diastolic HF, is increasingly recognized as a health care challenge. Guidelines have been issued for the classification, diagnosis, and prevention of HF from diastolic dysfunction, but treatment of this condition remains problematic. Antihypertensive agents that have been proven in clinical trials to improve outcomes in HF with systolic dysfunction, such as angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, and β-blockers, have not yet demonstrated comparable benefits in patients with diastolic dysfunction. Combination therapy using an antagonist of the renin-angiotensin-aldosterone system and a calcium-channel blocker has potential advantages over monotherapy and is being explored in several ongoing clinical trials.

Keywords: Angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, systolic dysfunction, left ventricular

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 Dr. Gaddam is a postdoctoral fellow supported by Grant NHLBI T32 HL007457. Dr. Oparil is the recipient of Grants-in-Aid from Abbott Laboratories, Astra Zeneca, Aventis, Biovail, Boehringer Ingelheim, Bristol Myers-Squibb, Forest Laboratories, GlaxoSmithKline, Novartis, Merck & Co, Pfizer, Daiichi-Sankyo Pharma, Sanofi-Aventis, and Schering-Plough. Dr. Oparil is a consultant for Bristol-Myers Squibb, Daiichi-Sankyo, Merck & Co., Novartis, Pfizer, Sanofi Aventis, and The Salt Institute.

PII: S1933-1711(08)00140-X

doi:10.1016/j.jash.2008.06.004

Journal of the American Society of Hypertension
Volume 3, Issue 1 , Pages 52-68, January 2009