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Beetroot Juice, Exercise and a Heart Drug Face Off in Hypertrophic Cardiomyopathy

A 168-patient trial pits lifestyle changes against sacubitril/valsartan to improve function and quality of life in HCM patients.

Tuesday, July 7, 2026 1 view
Published in Exercise & Cardiovascular Aging Trials
A glass of deep red beetroot juice next to a pill organizer and a heart rate monitor on a clinical desk, with an echocardiogram image in the background

Summary

Hypertrophic cardiomyopathy, the most common genetic cardiovascular disease, leaves many patients with limited exercise capacity and poor quality of life despite existing treatments. This completed Phase 2 pilot trial enrolled 168 patients across five centers using a three-arm design to compare lifestyle intervention (structured physical activity with dietary nitrate supplementation via concentrated beetroot juice) against the drug sacubitril/valsartan, an angiotensin receptor neprilysin inhibitor already proven to reduce hospitalizations in heart failure. Researchers wanted to know whether either strategy could meaningfully improve functional capacity, heart structure and function, and patient-reported quality of life. The trial was completed in June 2022, and results could inform how clinicians approach HCM management beyond conventional symptom control.

Detailed Summary

Hypertrophic cardiomyopathy is the most common genetic cardiovascular disease, with a broad spectrum of severity ranging from asymptomatic to severely limiting. Treatment options remain limited, focused mainly on symptom relief rather than modifying the underlying disease process. Finding interventions that genuinely improve exercise capacity and quality of life in HCM patients is a pressing clinical priority.

This five-center, open-label, three-arm Phase 2 pilot trial enrolled 168 patients with HCM to evaluate two distinct intervention strategies. One arm was a lifestyle intervention combining structured physical activity with inorganic nitrate supplementation in the form of concentrated nitrate-rich beetroot juice. Another arm was a pharmacological intervention using sacubitril/valsartan, an angiotensin receptor neprilysin inhibitor that has demonstrated mortality and hospitalization benefits in heart failure populations. The exact composition of the third arm is not specified in the available abstract.

The biological rationale for each arm is well grounded. Dietary nitrate improves vasodilation, cardiac output reserve, and reduces arterial wave reflections linked to left ventricular diastolic dysfunction and remodeling. Exercise training consistently raises exercise tolerance in HCM, even if it has limited effects on cardiac morphology or function. Sacubitril/valsartan has been shown to improve cardiac function and exercise tolerance in heart failure, mechanisms potentially relevant to HCM pathophysiology.

Primary outcomes focused on functional capacity, clinical phenotypic markers, and quality of life. Results from this completed trial have not yet been incorporated into major guidelines, and published outcome data were not available in the abstract reviewed here.

If either intervention proves effective, the implications are substantial. A safe, low-cost lifestyle protocol involving beetroot juice and exercise could be deployed broadly, while sacubitril/valsartan would represent a repurposed drug with a mechanistic rationale for HCM. Clinicians managing HCM patients should watch for full publication of these results.

Key Findings

  • Trial compared beetroot juice plus exercise against sacubitril/valsartan in 168 HCM patients across five centers.
  • Dietary nitrate targets vasodilation and diastolic dysfunction, both central defects in hypertrophic cardiomyopathy.
  • Sacubitril/valsartan reduces death and hospitalization in heart failure, providing a mechanistic rationale for HCM use.
  • Exercise training reliably boosts exercise tolerance in HCM even when it does not alter cardiac structure.
  • Study completed June 2022; full results could inform the first evidence-based lifestyle or drug protocol for HCM.

Methodology

Open-label, three-arm pilot randomized controlled trial conducted across five UK centers, enrolling 168 patients with confirmed hypertrophic cardiomyopathy. Interventions ran from 2019 through June 2022. The open-label design limits blinding, and the pilot scale means the study may not be fully powered for definitive efficacy conclusions.

Study Limitations

Summary is based on the abstract only; primary outcome data and full statistical results are not yet available for review. The open-label design introduces performance and detection bias. As a pilot trial, the 168-patient enrollment may limit statistical power to detect modest but clinically meaningful differences between arms.

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