Effects of spironolactone on ventricular-arterial coupling in patients with chronic systolic heart failure and mild symptoms

Clin Res Cardiol. 2015 Dec;104(12):1078-87. doi: 10.1007/s00392-015-0877-5. Epub 2015 Jun 10.

Abstract

Background: Several studies demonstrated that mineralocorticoid receptor antagonists (MRAs) are able to prevent myocardial and vascular fibrosis, and left ventricular (LV) remodeling in patients with systolic chronic heart failure (HF) and mild symptoms. Ventricular-arterial coupling (VAC) should be influenced by anti-fibrotic interventions. We have assessed the effects of spironolactone on VAC and its components, aortic elastance (Ea) and end-systolic LV elastance (Ees), in patients with HF.

Methods and results: Changes from baseline in VAC were compared between 65 patients treated with spironolactone and 32 controls not receiving MRAs. All patients had HF, reduced LVEF with reduced LV ejection fraction (LVEF) and New York Heart Association (NYHA) functional class I-II symptoms, and underwent transthoracic echocardiography at baseline and after 6 months. VAC was estimated by the modified single-beat method as Ea/Ees. Parameters of LV function improved after 6 month treatment with spironolactone with an increase in the LVEF from 34 ± 8 to 39 ± 8 % (p < 0.001). Spironolactone increased Ees from 1.32 ± 0.38 to 1.57 ± 0.42 mmHg/mL (p < 0.001) and reduced VAC from 2.03 ± 0.59 to 1.66 ± 0.31 (p < 0.001), but did not affect Ea and V0 (LV volume at end-systolic pressure of 0 mmHg). No change in any of these parameters occurred in the control group.

Conclusions: 6-month therapy with spironolactone improved VAC mainly through its effect on Ees in patients with mild HF.

Keywords: Heart failure; Mineralocorticoid receptor antagonists; Modified single-beat method; Ventricular-arterial coupling.

Publication types

  • Controlled Clinical Trial

MeSH terms

  • Aged
  • Echocardiography
  • Female
  • Follow-Up Studies
  • Heart Failure, Systolic / drug therapy*
  • Heart Failure, Systolic / physiopathology
  • Heart Ventricles / physiopathology
  • Humans
  • Male
  • Middle Aged
  • Mineralocorticoid Receptor Antagonists / pharmacology
  • Mineralocorticoid Receptor Antagonists / therapeutic use*
  • Prospective Studies
  • Spironolactone / pharmacology
  • Spironolactone / therapeutic use*
  • Ventricular Dysfunction, Left / drug therapy*
  • Ventricular Dysfunction, Left / physiopathology
  • Ventricular Function, Left / drug effects
  • Ventricular Remodeling / drug effects

Substances

  • Mineralocorticoid Receptor Antagonists
  • Spironolactone