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Effect of Inorganic Nitrite vs Placebo on Exercise Capacity Among Patients With Heart Failure With Preserved Ejection Fraction The INDIE-HFpEF Randomized Clinical Trial

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  • 05/21/2025
Type of Material
Authors
    Barry A. Borlaug, Mayo ClinicKevin J. Anstrom, Duke UniversityGregory D. Lewis, Harvard Medical SchoolSanjiv J. Shah, Northwestern UniversityJames A. Levine, Mayo ClinicGabe A. Koepp, Mayo ClinicMichael M. Givertz, Harvard Medical SchoolG. Michael Felker, Duke UniversityMartin M. LeWinter, University of VermontDouglas L. Mann, Washington UniversityKenneth B. Margulies, University of PennsylvaniaAndrew L Smith, Emory UniversityW. H.Wilson Tang, Cleveland ClinicDavid J. Whellan, Thomas Jefferson UniversityHorng H. Chen, Mayo ClinicVictor G. Davila-Roman, Washington UniversitySteven McNulty, Duke UniversityPatrice Desvigne-Nickens, National Heart, Lung, and Blood InstituteAdrian F. Hernandez, Duke UniversityEugene Braunwald, Harvard Medical SchoolMargeret M. Redfield, Mayo Clinic
Language
  • English
Date
  • 2018-11-06
Publisher
  • American Medical Association (AMA): JAMA
Publication Version
Copyright Statement
  • © 2018 American Medical Association. All rights reserved.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0098-7484
Volume
  • 320
Issue
  • 17
Start Page
  • 1764
End Page
  • 1773
Grant/Funding Information
  • This work was funded by the Heart Failure Clinical Research Network, which is supported by the NHLBI/NIH (grants U10 HL084904 [awarded to the coordinating center]; U10 HL110312; U10 HL110337; U10 HL110342; U10 HL110262; U10 HL110297; U10 HL110302; U10 HL110309; U10 HL110336; and U10 HL110338 [awarded to the regional clinical centers]); and Savara Therapeutics.
Supplemental Material (URL)
Abstract
  • Importance: There are few effective treatments for heart failure with preserved ejection fraction (HFpEF). Short-term administration of inorganic nitrite or nitrate preparations has been shown to enhance nitric oxide signaling, which may improve aerobic capacity in HFpEF. Objective: To determine the effect of 4 weeks' administration of inhaled, nebulized inorganic nitrite on exercise capacity in HFpEF. Design, Setting, and Participants: Multicenter, double-blind, placebo-controlled, 2-treatment, crossover trial of 105 patients with HFpEF. Participants were enrolled from July 22, 2016, to September 12, 2017, at 17 US sites, with final date of follow-up of January 2, 2018. Interventions: Inorganic nitrite or placebo administered via micronebulizer device. During each 6-week phase of the crossover study, participants received no study drug for 2 weeks (baseline/washout) followed by study drug (nitrite or placebo) at 46 mg 3 times a day for 1 week followed by 80 mg 3 times a day for 3 weeks. Main Outcomes and Measures: The primary end point was peak oxygen consumption (mL/kg/min). Secondary end points included daily activity levels assessed by accelerometry, health status as assessed by the Kansas City Cardiomyopathy Questionnaire (score range, 0-100, with higher scores reflecting better quality of life), functional class, cardiac filling pressures assessed by echocardiography, N-terminal fragment of the prohormone brain natriuretic peptide levels, other exercise indices, adverse events, and tolerability. Outcomes were assessed after treatment for 4 weeks. Results: Among 105 patients who were randomized (median age, 68 years; 56% women), 98 (93%) completed the trial. During the nitrite phase, there was no significant difference in mean peak oxygen consumption as compared with the placebo phase (13.5 vs 13.7 mL/kg/min; difference, -0.20 [95% CI, -0.56 to 0.16]; P =.27). There were no significant between-treatment phase differences in daily activity levels (5497 vs 5503 accelerometry units; difference, -15 [95% CI, -264 to 234]; P =.91), Kansas City Cardiomyopathy Questionnaire Clinical Summary Score (62.6 vs 61.9; difference, 1.1 [95% CI, -1.4 to 3.5]; P =.39), functional class (2.5 vs 2.5; difference, 0.1 [95% CI, -0.1 to 0.2]; P =.43), echocardiographic E/e′ ratio (16.4 vs 16.6; difference, 0.1 [95% CI, -1.2 to 1.3]; P =.93), or N-terminal fragment of the prohormone brain natriuretic peptide levels (520 vs 533 pg/mL; difference, 11 [95% CI, -53 to 75]; P =.74). Worsening heart failure occurred in 3 participants (2.9%) during the nitrite phase and 8 (7.6%) during the placebo phase. Conclusions and Relevance: Among patients with HFpEF, administration of inhaled inorganic nitrite for 4 weeks, compared with placebo, did not result in significant improvement in exercise capacity. Trial Registration: ClinicalTrials.gov Identifier: NCT02742129.
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  • Health Sciences, Medicine and Surgery

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