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Systolic blood pressure and cardiovascular outcomes in heart failure with preserved ejection fraction: an analysis of the TOPCAT trial.

Publication ,  Journal Article
Selvaraj, S; Claggett, B; Shah, SJ; Anand, I; Rouleau, JL; Desai, AS; Lewis, EF; Pitt, B; Sweitzer, NK; Pfeffer, MA; Solomon, SD
Published in: Eur J Heart Fail
March 2018

AIMS: Recent guidelines have advocated for stricter systolic blood pressure (SBP) control in heart failure with preserved ejection fraction (HFpEF), though data regarding the optimal SBP in HFpEF are sparse. METHODS AND RESULTS: We analysed participants from the Americas from the Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist (TOPCAT) study with available baseline and 8-week visit SBP data (n = 1645). We related baseline SBP to several efficacy and safety outcomes. To determine whether blood pressure lowering was responsible for the potential beneficial effects of spironolactone observed in the Americas, we assessed the randomized treatment adjusting for baseline and change in 8-week SBP. The average age was 71.7 ± 9.7 years, 50% were women, and 79% were White. Patients in the lowest baseline SBP quartile were less often female, more often White, had lower body mass index, lower baseline diastolic blood pressure and pulse pressure, and more often had atrial fibrillation. After multivariable adjustment, there was no relationship observed between baseline SBP quartiles and any outcome. Spironolactone reduced SBP by 4.4 ± 0.6 mmHg compared with placebo (and consistently across baseline SBP quartiles). There was minimal change in the treatment effect for all outcomes after adjusting for baseline SBP and 8-week change in SBP. CONCLUSION: No relationship was observed between baseline SBP quartiles and outcomes in TOPCAT. The anti-hypertensive effects of spironolactone did not account for the potential benefit in cardiovascular outcomes in the Americas.

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Published In

Eur J Heart Fail

DOI

EISSN

1879-0844

Publication Date

March 2018

Volume

20

Issue

3

Start / End Page

483 / 490

Location

England

Related Subject Headings

  • Treatment Outcome
  • Time Factors
  • Systole
  • Stroke Volume
  • Spironolactone
  • Retrospective Studies
  • Mineralocorticoid Receptor Antagonists
  • Middle Aged
  • Male
  • Humans
 

Citation

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Selvaraj, S., Claggett, B., Shah, S. J., Anand, I., Rouleau, J. L., Desai, A. S., … Solomon, S. D. (2018). Systolic blood pressure and cardiovascular outcomes in heart failure with preserved ejection fraction: an analysis of the TOPCAT trial. Eur J Heart Fail, 20(3), 483–490. https://doi.org/10.1002/ejhf.1060
Selvaraj, Senthil, Brian Claggett, Sanjiv J. Shah, Inder Anand, Jean L. Rouleau, Akshay S. Desai, Eldrin F. Lewis, et al. “Systolic blood pressure and cardiovascular outcomes in heart failure with preserved ejection fraction: an analysis of the TOPCAT trial.Eur J Heart Fail 20, no. 3 (March 2018): 483–90. https://doi.org/10.1002/ejhf.1060.
Selvaraj S, Claggett B, Shah SJ, Anand I, Rouleau JL, Desai AS, et al. Systolic blood pressure and cardiovascular outcomes in heart failure with preserved ejection fraction: an analysis of the TOPCAT trial. Eur J Heart Fail. 2018 Mar;20(3):483–90.
Selvaraj, Senthil, et al. “Systolic blood pressure and cardiovascular outcomes in heart failure with preserved ejection fraction: an analysis of the TOPCAT trial.Eur J Heart Fail, vol. 20, no. 3, Mar. 2018, pp. 483–90. Pubmed, doi:10.1002/ejhf.1060.
Selvaraj S, Claggett B, Shah SJ, Anand I, Rouleau JL, Desai AS, Lewis EF, Pitt B, Sweitzer NK, Pfeffer MA, Solomon SD. Systolic blood pressure and cardiovascular outcomes in heart failure with preserved ejection fraction: an analysis of the TOPCAT trial. Eur J Heart Fail. 2018 Mar;20(3):483–490.
Journal cover image

Published In

Eur J Heart Fail

DOI

EISSN

1879-0844

Publication Date

March 2018

Volume

20

Issue

3

Start / End Page

483 / 490

Location

England

Related Subject Headings

  • Treatment Outcome
  • Time Factors
  • Systole
  • Stroke Volume
  • Spironolactone
  • Retrospective Studies
  • Mineralocorticoid Receptor Antagonists
  • Middle Aged
  • Male
  • Humans