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Modification of ventriculo-arterial coupling by spironolactone in nonischemic dilated cardiomyopathy.
Lawson, Mark A; Hansen, David E; Gupta, Deepak K; Bell, Susan P; Adkisson, Douglas W; Mallugari, Ravinder R; Sawyer, Douglas B; Ooi, Henry; Kronenberg, Marvin W.
Afiliação
  • Lawson MA; VA Tennessee Valley Health Care System, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
  • Hansen DE; VA Tennessee Valley Health Care System, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
  • Gupta DK; VA Tennessee Valley Health Care System, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
  • Bell SP; VA Tennessee Valley Health Care System, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
  • Adkisson DW; VA Tennessee Valley Health Care System, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
  • Mallugari RR; VA Tennessee Valley Health Care System, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
  • Sawyer DB; VA Tennessee Valley Health Care System, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
  • Ooi H; VA Tennessee Valley Health Care System, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
  • Kronenberg MW; VA Tennessee Valley Health Care System, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
ESC Heart Fail ; 8(2): 1156-1166, 2021 04.
Article em En | MEDLINE | ID: mdl-33403831
AIMS: We sought to clarify the role of ventriculo-arterial (V-A) coupling in the treatment of nonischemic dilated cardiomyopathy (NIDCM) by adding a mineralocorticoid receptor antagonist (MRA) to conventional anti-failure therapy. METHODS AND RESULTS: We employed cardiac magnetic resonance imaging to quantify left ventricular (LV) contractility and V-A coupling in normal subjects at rest (n = 11) and in patients with NIDCM (n = 12) before and after long term anti-failure therapy, in which MRA was added to conventional anti-failure therapy. After ≥6 months' treatment in NIDCM patients, LV volumes and mass decreased, and the LV ejection fraction increased from a median of 24% (17, 27) (interquartile range IQR) to 47 (42, 52) (P < 0.002), with a marked reduction in arterial elastance (Ea) from 2.89 mmHg/mL (2.34, 4.0) to 1.50 (1.29, 1.95) (P < 0.002), similar to Ea of normal subjects, 1.53 (1.34, 1.67) (P > 0.05). The V-A coupling ratio, Ea/end-systolic elastance (single-beat method), decreased by -1.08 (-1.96, -0.55), (P = 0.003), as did Ea/end-systolic pressure/end-systolic pressure ratio, -0.54 (0.35, 0.87), (P = 0.002). The preload recruitable stroke work (PRSW) increased as did PRSW indexed for Ea (both P = 0.002), which reflected 'total circulatory performance'. CONCLUSIONS: In NIDCM, adding MRA to conventional anti-failure therapy markedly improved LV ejection fraction and reduced peripheral vascular resistance, due to both improved LV contractility and especially to enhanced V-A coupling, as Ea decreased to normal. Total circulatory performance was a sensitive indicator of both LV pump performance and the arterial loading conditions.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espironolactona / Cardiomiopatia Dilatada Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espironolactona / Cardiomiopatia Dilatada Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article