Limitation of Excessive Extracellular Matrix Turnover May Contribute to Survival Benefit of Spironolactone Therapy in Patients With Congestive Heart Failure
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- 28 November 2000
- journal article
- clinical trial
- Published by Wolters Kluwer Health in Circulation
- Vol. 102 (22) , 2700-2706
- https://doi.org/10.1161/01.cir.102.22.2700
Abstract
Background —In congestive heart failure (CHF), extracellular matrix turnover is a major determinant of cardiac remodeling. It has been suggested that spironolactone may decrease cardiac fibrosis. We investigated the interactions between serum markers of cardiac fibrosis and the effect of spironolactone on outcome in patients with CHF. Methods and Results —A sample of 261 patients from the Randomized Aldactone Evaluation Study (RALES) were randomized to placebo or spironolactone (12.5 to 50 mg daily). Serum procollagen type I carboxy-terminal peptide, procollagen type I amino-terminal peptide, and procollagen type III amino-terminal peptide (PIIINP) were assessed at baseline and at 6 months. Baseline PIIINP >3.85 μg/L was associated with an increased risk of death (relative risk [RR] 2.36, 95% CI 1.34 to 4.18) and of death+hospitalization (RR 1.83, 95% CI 1.18 to 2.83). At 6 months, markers decreased in the spironolactone group but remained unchanged in the placebo group. The spironolactone effect on outcome was significant only in patients with above-median baseline levels of markers. RR (95% CI) values for death among patients receiving spironolactone were 0.44 (0.26 to 0.75) and 1.11 (0.66 to 1.88) in subgroups of PIIINP levels above and below the median, respectively. Similarly, RR (95% CI) values for death+hospitalization among patients receiving spironolactone were 0.45 (0.29 to 0.71) and 0.85 (0.55 to 1.33), respectively. Conclusions —In patients with CHF, high baseline serum levels of markers of cardiac fibrosis synthesis are significantly associated with poor outcome and decrease during spironolactone therapy. The benefit from spironolactone was associated with higher levels of collagen synthesis markers. These results suggest that limitation of the excessive extracellular matrix turnover may be one of the various extrarenal mechanisms contributing to the beneficial effect of spironolactone in patients with CHF.Keywords
This publication has 28 references indexed in Scilit:
- Infarct scar: a dynamic tissueCardiovascular Research, 2000
- Aldosterone and Spironolactone in Heart FailureNew England Journal of Medicine, 1999
- The Effect of Spironolactone on Morbidity and Mortality in Patients with Severe Heart FailureNew England Journal of Medicine, 1999
- The aminoterminal propeptide of type III procollagen provides new information on prognosis after acute myocardial infarctionThe American Journal of Cardiology, 1995
- Temporal differences in fibroblast proliferation and phenotype expression in response to chronic administration of angiotensin II or aldosteroneJournal of Molecular and Cellular Cardiology, 1995
- Measuring extracellular matrix turnover in the serum of patients with idiopathic or ischemic dilated cardiomyopathy and impact on diagnosis and prognosisThe American Journal of Cardiology, 1995
- Increased cardiac types I and III collagen mRNAs in aldosterone-salt hypertension.Hypertension, 1994
- Mineralocorticoids, hypertension, and cardiac fibrosis.Journal of Clinical Investigation, 1994
- Quantitating coronary collateral flow velocity in patients during coronary angioplasty using a Doppler guidewireThe American Journal of Cardiology, 1993
- Studies on collagen in the experimental myocardial infarction.Japanese Circulation Journal, 1985