Natural history of markers of collagen turnover in patients with early diastolic dysfunction and impact of eplerenone

J Am Coll Cardiol. 2009 Oct 27;54(18):1674-82. doi: 10.1016/j.jacc.2009.08.021.

Abstract

Objectives: This study was designed to evaluate the impact of eplerenone on collagen turnover in preserved systolic function heart failure (HFPSF).

Background: Despite growing interest in abnormal collagen metabolism as a feature of HFPSF with diastolic dysfunction, the natural history of markers of collagen turnover and the impact of selective aldosterone antagonism on this natural history remains unknown.

Methods: We evaluated 44 patients with HFPSF, randomly assigned to control (n = 20) or eplerenone 25 mg daily (n = 24) for 6 months, increased to 50 mg daily from 6 to 12 months. Serum markers of collagen turnover and inflammation were analyzed at baseline and at 6 and 12 months and included pro-collagen type-I and -III aminoterminal peptides, matrix metalloproteinase type-2, interleukin-6 and -8, and tumor necrosis factor-alpha. Doppler-echocardiographic assessment of diastolic filling indexes and tissue Doppler analyses were also obtained.

Results: The mean age of the patients was 80 +/- 7.8 years; 46% were male; 64% were receiving an angiotensin-converting enzyme inhibitor, 34% an angiotensin-II receptor blocker, and 68% were receiving beta-blocker therapy. Pro-collagen type-III and -I aminoterminal peptides, matrix metalloproteinase type-2, interleukin-6 and -8, and tumor necrosis factor-alpha increased with time in the control group. Eplerenone treatment had no significant impact on any biomarker at 6 months but attenuated the increase in pro-collagen type-III aminoterminal peptide at 12 months (p = 0.006). Eplerenone therapy was associated with modest effects on diastolic function without any impact on clinical variables or brain natriuretic peptide.

Conclusions: This study demonstrates progressive increases in markers of collagen turnover and inflammation in HFPSF with diastolic dysfunction. Despite high background utilization of renin-angiotensin-aldosterone modulators, eplerenone therapy prevents a progressive increase in pro-collagen type-III aminoterminal peptide and may have a role in management of this disease. (The Effect of Eplerenone and Atorvastatin on Markers of Collagen Turnover in Diastolic Heart Failure; NCT00505336).

Trial registration: ClinicalTrials.gov NCT00094302 NCT00505336.

Publication types

  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Biomarkers / blood
  • Collagen Type I / blood*
  • Collagen Type III / blood*
  • Echocardiography, Doppler
  • Eplerenone
  • Female
  • Follow-Up Studies
  • Heart Failure, Diastolic / blood*
  • Heart Failure, Diastolic / drug therapy
  • Heart Failure, Diastolic / physiopathology
  • Heart Ventricles / diagnostic imaging
  • Heart Ventricles / physiopathology*
  • Humans
  • Male
  • Mineralocorticoid Receptor Antagonists / administration & dosage*
  • Procollagen / blood*
  • Prospective Studies
  • Radioimmunoassay
  • Spironolactone / administration & dosage
  • Spironolactone / analogs & derivatives*
  • Treatment Outcome

Substances

  • Biomarkers
  • Collagen Type I
  • Collagen Type III
  • Mineralocorticoid Receptor Antagonists
  • Procollagen
  • Spironolactone
  • Eplerenone

Associated data

  • ClinicalTrials.gov/NCT00094302
  • ClinicalTrials.gov/NCT00505336