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Myocardial Effects of Aldosterone Antagonism in Heart Failure With Preserved Ejection Fraction.
McDiarmid, Adam K; Swoboda, Peter P; Erhayiem, Bara; Bounford, Katrina A; Bijsterveld, Petra; Tyndall, Keith; Fent, Graham J; Garg, Pankaj; Dobson, Laura E; Musa, Tarique A; Foley, James R J; Witte, Klaus K; Kearney, Mark T; Greenwood, John P; Plein, Sven.
Afiliación
  • McDiarmid AK; Multidisciplinary Cardiovascular Research Centre and Leeds Institute of Cardiovascular and Metabolic Medicine University of Leeds United Kingdom.
  • Swoboda PP; Department of Cardiology Freeman Hospital Newcastle-upon-Tyne United Kingdom.
  • Erhayiem B; Multidisciplinary Cardiovascular Research Centre and Leeds Institute of Cardiovascular and Metabolic Medicine University of Leeds United Kingdom.
  • Bounford KA; Multidisciplinary Cardiovascular Research Centre and Leeds Institute of Cardiovascular and Metabolic Medicine University of Leeds United Kingdom.
  • Bijsterveld P; Leeds Teaching Hospitals NHS Trust Leeds United Kingdom.
  • Tyndall K; Multidisciplinary Cardiovascular Research Centre and Leeds Institute of Cardiovascular and Metabolic Medicine University of Leeds United Kingdom.
  • Fent GJ; Leeds Teaching Hospitals NHS Trust Leeds United Kingdom.
  • Garg P; Multidisciplinary Cardiovascular Research Centre and Leeds Institute of Cardiovascular and Metabolic Medicine University of Leeds United Kingdom.
  • Dobson LE; Multidisciplinary Cardiovascular Research Centre and Leeds Institute of Cardiovascular and Metabolic Medicine University of Leeds United Kingdom.
  • Musa TA; Multidisciplinary Cardiovascular Research Centre and Leeds Institute of Cardiovascular and Metabolic Medicine University of Leeds United Kingdom.
  • Foley JRJ; Multidisciplinary Cardiovascular Research Centre and Leeds Institute of Cardiovascular and Metabolic Medicine University of Leeds United Kingdom.
  • Witte KK; Multidisciplinary Cardiovascular Research Centre and Leeds Institute of Cardiovascular and Metabolic Medicine University of Leeds United Kingdom.
  • Kearney MT; Multidisciplinary Cardiovascular Research Centre and Leeds Institute of Cardiovascular and Metabolic Medicine University of Leeds United Kingdom.
  • Greenwood JP; Multidisciplinary Cardiovascular Research Centre and Leeds Institute of Cardiovascular and Metabolic Medicine University of Leeds United Kingdom.
  • Plein S; Multidisciplinary Cardiovascular Research Centre and Leeds Institute of Cardiovascular and Metabolic Medicine University of Leeds United Kingdom.
J Am Heart Assoc ; 9(1): e011521, 2020 01 07.
Article en En | MEDLINE | ID: mdl-31852424
ABSTRACT
Background Spironolactone may have prognostic benefit in selected patients with heart failure with preserved ejection fraction. This study assessed the myocardial tissue effects of spironolactone in heart failure with preserved ejection fraction. Methods and Results A 11 randomized controlled study of 6 months of spironolactone versus control in heart failure with preserved ejection fraction. The primary outcome was change in myocardial extracellular volume fraction by cardiovascular magnetic resonance as a surrogate of diffuse fibrosis. Of 55 randomized patients, 40 (20 women; age, 75.2±5.9 years) completed follow-up (19 treatment, 21 control). A significant change in extracellular volume over the study period was not seen (treatment, 28.7±3.7% versus 27.7±3.4% [P=0.14]; controls, 27.6±3.4% versus 28.3±4.4% [P=0.14]); however, the rate of extracellular volume expansion was decreased by spironolactone (-1.0±2.4% versus 0.8±2.2%). Indexed left ventricular mass decreased with treatment (104.4±26.6 versus 94.0±20.6 g/m2; P=0.001) but not in controls (101.4±29.4 versus 104.0±32.8 g/m2; P=0.111). Extracellular mass decreased by 13.8% (15.1±4.8 versus 13.0±3.4 g/m2; P=0.003), and cellular mass decreased by 8.3% (37.6±10.0 versus 34.3±7.9 g/m2; P=0.001) with spironolactone, but was static in controls. Conclusions Spironolactone did not lead to significant change in extracellular volume. However, spironolactone did decrease rate of extracellular expansion, with a decrease in the mass of both cellular and extracellular myocardial compartments. These data point to the mechanism of action of spironolactone in heart failure with preserved ejection fraction, including a direct tissue effect with a reduction in rate of myocardial fibrosis.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Espironolactona / Volumen Sistólico / Función Ventricular Izquierda / Remodelación Ventricular / Antagonistas de Receptores de Mineralocorticoides / Insuficiencia Cardíaca / Miocardio Tipo de estudio: Clinical_trials / Prognostic_studies País/Región como asunto: Europa Idioma: En Revista: J Am Heart Assoc Año: 2020 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Espironolactona / Volumen Sistólico / Función Ventricular Izquierda / Remodelación Ventricular / Antagonistas de Receptores de Mineralocorticoides / Insuficiencia Cardíaca / Miocardio Tipo de estudio: Clinical_trials / Prognostic_studies País/Región como asunto: Europa Idioma: En Revista: J Am Heart Assoc Año: 2020 Tipo del documento: Article