European Society of Cardiology
Skip navigation links
Home
About the ESC
Membership
Communities
Congresses
Education
Guidelines & Surveys
Journals
Initiatives
Welcome to the European Society of Cardiology. Our mission: to reduce the burden of cardiovascular disease in Europe
 

The mechanistic effects of spironalactone in diastolic heart failure: the Aldo-DHF study 

Hotline I - Late Breaking Trials on Prevention of Heart Failure

Topics: Heart Failure (HF)
Date: 26 Aug 2012
Munich, Germany – 26 August 2012: Mineralocorticoid receptor antagonists should be considered as a treatment option in hypertensive patients with diastolic heart failure, said Professor Burkert Pieske presenting results today of the Aldosterone Receptor Blockade in Diastolic Heart Failure (Aldo-DHF) study at ESC Congress 2012.

Behind his conclusion lay results showing that mineralocorticoid receptor blockade with spironolactone improves cardiac function and structure, reduces neuroendocrine activation, and effectively reduces blood pressure in a patient population with symptomatic predominantly hypertensive diastolic heart failure. However, results also showed that spironolactone did not improve exercise capacity or symptoms of heart failure.

As background to the study Professor Pieske, Head of Cardiology at the Medical University Graz in Austria, explained that diastolic heart failure (DHF) - also known as heart failure with preserved ejection fraction - is a condition which increasingly affects millions of people in Europe. Today, he said, more than half of all heart failure patients have DHF, as opposed to classical systolic heart failure, and DHF is the dominant form of heart failure in elderly patients, especially women. Patients suffer from poor quality of life, impaired exercise capacity and a high rate of hospitalisation and mortality.

"Mechanistically," said Professor Pieske, "the main underlying pathology is thought to be impaired filling of the left ventricle, often as a consequence of long-standing hypertension, diabetes, and other lifestyle-associated cardiovascular risks factors. However, despite the large number of affected patients and the poor outcome, no therapy has so far demonstrated therapeutic benefit.

"The neuroendocrine hormone aldosterone mediates, through mineralocorticoid receptors, adverse effects on cardiac function and remodelling, as well as on vascular stiffness. In consequence, aldosterone induces myocardial hypertrophy, fibrosis and diastolic dysfunction, all potential mechanistic factors in the pathology of diastolic heart failure. However, despite this mechanistic evidence and convincing benefits in systolic heart failure, aldosterone antagonism has never been tested in a large randomised multicentre trial in patients with DHF."

The Aldo-DHF trial was designed to test the hypothesis that 12 months treatment with the mineralocorticoid receptor antagonist spironolactone would improve cardiac function and structure, as well as exercise capacity and quality of life in patients with DHF. The study was an international multicentre Phase IIb trial funded after peer review by the German government within the Clinical Trial Research Program. 

Aldo-DHF prospectively randomised 422 patients with symptomatic DHF to either spironolactone (target dose, 25 mg/day) or placebo over a treatment period of 12 months. The two co-primary endpoints were changes in diastolic function (filling pressure, assessed non-invasively by tissue-Doppler derived E/é, an established and validated echocardiographic estimate of left ventricular filling pressure) and changes in maximal exercise capacity (peak oxygen consumption, VO2), assessed by bicycle spiroergometry after 12 months.

Secondary endpoints included other parameters of echocardiographic functional and structural cardiac abnormalities, submaximal exercise capacity, quality of life and NYHA class. Safety including classical side effects such as increase in serum potassium or decreases in renal function were also assessed.

Results showed that spironolactone significantly improved diastolic function (assessed as a significant decline in E/é), but did not change maximal exercise capacity (peak V02) after one year. Spironolactone also induced reverse cardiac remodelling and reduced left ventricular hypertrophy, a known detrimental consequence of hypertension and diabetes), NTproBNP plasma levels, and systolic and diastolic blood pressure.

However, spironolactone did not improve other measures of exercise capacity, NYHA class, or quality of life, but was shown to be safe, without relevant adverse events.

Results from the NIH-funded TOPCAT trial will show if these beneficial effects of spironolactone translate into better clinical outcome.

* The Aldo-DHF study was an international multicentre Phase IIb trial (with leading centres in Göttingen, Germany, and Graz, Austria) funded after peer review by the Clinical Trial Research Program of the German Government.

Authors: Prof Burkert Mathias Pieske (Austria), Medical University Graz

ESC Press Office

For background information, please contact the ESC Press Office.
For independent comment on site, please contact Tanya Kenny, +4917610572544

Notes to editor

About the European Society of Cardiology
The European Society of Cardiology (ESC) represents more than 75,000 cardiology professionals across Europe and the Mediterranean. Its mission is to reduce the burden of cardiovascular disease in Europe.

About ESC Congress 2012
ESC Congress 2012 will take place from 25 to 29 August at the Messe München centre in Munich, Germany. Information on the scientific programme is available here. More information on ESC Congress 2012 is available from the ESC Press Office or contact us at press@escardio.org


References This press release accompanies both a presentation and an ESC press conference at the ESC Congress 2012. Edited by the ESC from material supplied by the investigator himself/herself, this press release does not necessarily reflect the opinion of the European Society of Cardiology. The content of the press release has been approved by the investigator.

Refers to session: Hot Line I: Late Breaking Trials on Prevention to Heart Failure

Refers to press conference:  Hotline I - Late Breaking Trials on Prevention of Heart Failure