Literature DB >> 24846808

Use of isosorbide dinitrate and hydralazine in African-Americans with heart failure 9 years after the African-American Heart Failure Trial.

Keith Copelin Ferdinand1, Uri Elkayam2, Donna Mancini3, Elizabeth Ofili4, Ileana Piña5, Inder Anand6, Arthur Michael Feldman7, Dennis McNamara8, Christopher Leggett9.   

Abstract

The 2013 American College of Cardiology Foundation/American Heart Association guidelines recommend combined isosorbide dinitrate (ISDN) and hydralazine to reduce mortality and morbidity for African-Americans with symptomatic heart failure (HF) and reduced ejection fraction, currently receiving optimal medical therapy (class I, level A). Nitrates can alleviate HF symptoms, but continuous use is limited by tolerance. Hydralazine may mitigate nitrate tolerance, and the ISDN-hydralazine combination in the Vasodilators in Heart Failure Trial (V-HeFT) I improved survival and exercise tolerance in men with dilated cardiomyopathy or HF with reduced ejection fraction, most notably in self-identified black participants. In the subsequent V-HeFT II, survival was greater with enalapril than with ISDN-hydralazine in the overall cohort, but mortality rate was similar in the enalapril and ISDN-hydralazine groups in the self-identified black patients. Consequently, in the African-American Heart Failure Trial (A-HeFT) in self-identified black patients with symptomatic HF, adding a fixed-dose combination ISDN-hydralazine to modern guideline-based care improved outcomes versus placebo, including all-cause mortality, and led to early trial termination. Hypertension underlies HF, especially in African-Americans; the A-HeFT and its substudies demonstrated not only improvements in echocardiographic parameters, morbidity, and mortality but also a decrease in hospitalizations, potentially affecting burgeoning HF health-care costs. Genetic characteristics may, therefore, determine response to ISDN-hydralazine, and the Genetic Risk Assessment in Heart Failure substudy demonstrated important hypothesis-generating pharmacogenetic data.
Copyright © 2014 Elsevier Inc. All rights reserved.

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Year:  2014        PMID: 24846808     DOI: 10.1016/j.amjcard.2014.04.018

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  6 in total

1.  The Role of Hypertension in Race-Ethnic Disparities in Cardiovascular Disease.

Authors:  Pelbreton C Balfour; Carlos J Rodriguez; Keith C Ferdinand
Journal:  Curr Cardiovasc Risk Rep       Date:  2015-04

Review 2.  Leveraging Signaling Pathways to Treat Heart Failure With Reduced Ejection Fraction.

Authors:  Miguel Pinilla-Vera; Virginia S Hahn; David A Kass
Journal:  Circ Res       Date:  2019-05-24       Impact factor: 17.367

3.  Direct Cα-heteroarylation of structurally diverse ethers via a mild N-hydroxysuccinimide mediated cross-dehydrogenative coupling reaction.

Authors:  Shihui Liu; Aoxia Liu; Yongqiang Zhang; Wei Wang
Journal:  Chem Sci       Date:  2017-03-24       Impact factor: 9.825

4.  Underuse of hydralazine and isosorbide dinitrate for heart failure in patients of African ancestry: a cross-European survey.

Authors:  Lizzy M Brewster
Journal:  ESC Heart Fail       Date:  2019-03-20

Review 5.  Heart Failure in Minority Populations - Impediments to Optimal Treatment in Australian Aborigines.

Authors:  Pupalan Iyngkaran; Nadarajan Kangaharan; Hendrik Zimmet; Margaret Arstall; Rob Minson; Merlin C Thomas; Peter Bergin; John Atherton; Peter MacDonald; David L Hare; John D Horowitz; Marcus Ilton
Journal:  Curr Cardiol Rev       Date:  2016

6.  Developing a roadmap to improve trial delivery for under-served groups: results from a UK multi-stakeholder process.

Authors:  Miles D Witham; Eleanor Anderson; Camille Carroll; Paul M Dark; Kim Down; Alistair S Hall; Joanna Knee; Rebecca H Maier; Gail A Mountain; Gary Nestor; Laurie Oliva; Sarah R Prowse; Amanda Tortice; James Wason; Lynn Rochester
Journal:  Trials       Date:  2020-08-01       Impact factor: 2.279

  6 in total

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