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Effect of Dietary Nitrate Ingestion in Heart Failure

Investigation of Dietary Nitrate Optimisation by Hyperuricaemia Stratification in Heart Failure

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03511248
Acronym
DiNOmo-HF
Enrollment
2
Registered
2018-04-27
Start date
2018-06-01
Completion date
2025-01-07
Last updated
2025-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure, Heart Failure, Systolic

Keywords

Heart Failure, Heart Failure with Reduced Ejection Fraction, Nitric Oxide, Inorganic Nitrate

Brief summary

This study evaluates the addition of inorganic dietary nitrate to the optimal treatment of patients diagnosed with heart failure with reduced ejection fraction. Some vegetables contain large amounts of inorganic nitrate, and research suggests that this nitrate has beneficial effects on the heart and blood vessels. We have shown in lab experiments that nitrate has positive effects on the heart. We wish to test whether dietary nitrate might be useful in halting deterioration and/or improving heart function in patients with heart failure, with a specific focus on a marker of poor outcome in heart failure: high uric acid levels. Half of the patients will receive nitrate-rich beetroot juice, and the other half a nitrate-deplete placebo beetroot juice.

Detailed description

Background: Heart failure (HF) affects 1-2% of those under 70 years, and 10-20% of those over 70 years in developed countries; approximately 900,000 people in the UK suffer with HF. Despite several promising pre-clinical targets, clinical translation has been disappointing, with very few successful phase 3 studies of new HF therapeutics. Dysfunction of the classical pathways that underlie endothelial nitric oxide (NO) production, with deficient cardiac constitutive NO supply, are thought to play a major role in the pathogenesis of HF. It has been mooted that novel strategies that replace/restore this diminished NO have therapeutic potential. The organic nitrates, as a method of NO delivery, provide an efficacious treatment in the acute HF setting. However, the development of tolerance, tachyphylaxis, and endothelial dysfunction with long-term use severely limits their utility in chronic heart disease. Alternative methods for sustained NO delivery without tolerance are therefore of interest. Recent clinical research demonstrates that inorganic nitrate offers this possibility through sequential chemical reduction, first via the enterosalivary circuit to nitrite, and subsequently from nitrite to NO. In particular, pre-clinical research suggests that delivery of NO via this pathway imparts benefit in HF models. Dietary inorganic nitrate is known to provide a safe and non-invasive method to elevate NO in humans, and a once daily dose (5-6mmol), in the form of a beetroot juice, can improve vascular function and reduce blood pressure in hypertensives. Inorganic nitrate as a HF treatment is particularly exciting since a key pathway involved in the generation of NO from nitrate is xanthine oxidoreductase (XOR); an enzyme upregulated in HF. Conventionally, XOR is considered detrimental as it generates superoxide and uric acid; both exert negative effects on cardiac function, and are associated with worse outcomes in HF. However, XOR also plays an important role in the second step of nitrate bioactivation: conversion of nitrite to NO in the heart. Importantly, we have hypothesised that in an environment of elevated XOR activity, such as HF, delivery of inorganic nitrate to the body would result in reductions in superoxide/uric acid with concomitant elevations in NO. This might prove more efficacious than simply inhibiting the enzyme using classical inhibitors. Importantly, a recent study (EXACT-HF) has shown a trend for reduced HF re-hospitalisations in those with XOR inhibition via allopurinol; it has been suggested that greater benefits might be seen if these effects are coupled with NO delivery. Research Hypothesis and Aims: We aim to investigate whether dietary inorganic nitrate provides benefit in patients with HF. We will determine whether inorganic nitrate delivery by elevating nitrite, delivers substrate to XOR resulting in a two-fold benefit: increasing NO production, whilst concomitantly reducing superoxide and uric acid levels. Plan of Investigation: a randomised double-blind placebo-controlled parallel two-limb study in New York Heart Association (NHYA) class II-III HF patients. Patients with left ventricular ejection fraction (LVEF) \<50% and elevated NT-proBNP/ BNP levels will be enrolled and stratified by degree of hyperuricaemia. 92-patients will receive a once daily dose of nitrate-rich beetroot juice (versus nitrate-deplete beetroot juice) for 12-weeks. The study is powered for significant reductions in hyperuricaemia. Powered secondary outcomes include circulating nitrite/nitrate levels, nitrite reductase activity, and a difference in LVEF from baseline by contrast echocardiography. A number of mechanistic exploratory outcomes will also be reported, including assessments of oxidative stress, erythrocytic XOR activity, 6-minute walk test, quality of life questionnaire and levels of NT-proBNP/BNP as surrogate measures of cardiac dysfunction. Benefits: This trial if positive will identify a new, safe and easy-to-deliver therapeutic option for HF patients. The NHS would benefit by providing a new inexpensive pharmacotherapy for a disease with significant unmet need and increasing burden to the health service.

Interventions

DIETARY_SUPPLEMENTNitrate-rich Beetroot Juice

The beetroot juice contains approximately 100kcal per 100mL of juice, equivalent to a glass of orange juice; the volume of juice per day for the study is 70mL. Volunteers will be informed that an average woman weighing 65kg should not consume more than 2000kcal per day, and an average man of 75kg not more than 2500kcal per day.

The beetroot juice contains approximately 100kcal per 100mL of juice, equivalent to a glass of orange juice; the volume of juice per day for the study is 70mL. Volunteers will be informed that an average woman weighing 65kg should not consume more than 2000kcal per day, and an average man of 75kg not more than 2500kcal per day.

Sponsors

Queen Mary University of London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Double-blind study, with randomisation undertaken by Barts Cardiovascular Clinical Trials Unit

Intervention model description

Randomised double-blind placebo-controlled parallel two-limb study

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age ≥18 years 2. Diagnosed with heart failure with reduced ejection fraction on the basis of: 1. LVEF ≤50% as assessed by Echocardiography (or cardiac MRI) 2. raised BNP and/or NT-proBNP levels placing patients in the high risk category, to ensure heart failure is the cause of symptoms: * stable heart failure: NT-proBNP \>600pg/mL and BNP \>150pg/mL * hospitalisation within 12 months: NT-proBNP \>400pg/mL and BNP \>100pg/mL 3. NYHA Class II-III symptoms 4. On optimally-tolerated, stable (\>12 weeks) prognostic medical therapy (beta-blocker, ACE-inhibitor or ARB, mineralocorticoid therapy if deemed necessary) 5. No heart failure-related hospitalisation for \>12 weeks 6. Clinic systolic blood pressure ≥95mmHg 7. Able and willing to give written informed consent The intervention with dietary nitrate is intentionally designed to be in addition to the patient's own lifestyle. There will be no restrictions placed on diet, anti-oxidant supplements or prescription medications, other than those listed in the

Exclusion criteria

below.

Design outcomes

Primary

MeasureTime frameDescription
Change in serum uric acid levels12 +/- 2 weeksUric acid is a prognostic marker in patients with heart failure. The intervention proposed acts on the enzyme, xanthine oxidoreductase (XOR), that produces uric acid. We will therefore measure the change in serum uric acid level from baseline to assess whether dietary nitrate treatment decreases hyperuricaemia. We will stratify uric acid levels and undertake analysis between strata.

Secondary

MeasureTime frameDescription
Changes in plasma nitrate12 +/- 2 weeksWe will measure the change in nitrate levels in plasma using ozone chemiluminescence, which measures the consumed dose of inorganic nitrate consumed, as the first step in the enterosalivary circuit.
Changes in plasma nitrite12 +/- 2 weeksWe will measure the change in nitrite levels in plasma using ozone chemiluminescence, measuring the conversion of nitrate to nitrite which the enzyme XOR uses to form the biologically active metabolite, nitric oxide.
Changes in cGMP as a marker for Nitric Oxide12 +/- 2 weeksWe will measure the change in cGMP levels using an ELISA assay, as a stable and measurable surrogate of the biologically active product, nitric oxide.
Changes in cardiac pump function12 +/- 2 weeksUsing contrast Echocardiography, we will measure the change in left ventricular ejection fraction from baseline following intervention.

Other

MeasureTime frameDescription
Change in NT-proBNP12 +/- 2 weeksAnalysis of this important natriuretic peptide
Change in BNP12 +/- 2 weeksAnalysis of this important natriuretic peptide
Change in high sensitivity C-Reactive Protein12 +/- 2 weeksAnalysis of the highly sensitive marker of inflammation
Change in lipid levels (LDL, triglycerides, HDL, total cholesterol)12 +/- 2 weeksAnalysis of lipids
Contrast Echocardiography: ventricular function12 +/- 2 weeksMeasurement of cardiac ventricular function using cardiac MRI (ejection fraction)
Contrast Echocardiography: ventricular volumes12 +/- 2 weeksMeasurement of cardiac ventricular volumes using cardiac MRI
Changes in markers of oxidative stress: MDA12 +/- 2 weeksMeasured using ELISA and used collectively with oxidised LDL and TBAR assays to determine oxidative stress
Changes in resting cardiac electrical activity12 +/- 2 weeksAs determined by electrocardiogram analysis
6-minute Walk Test12 +/- 2 weeksFunctional assessment of exercise capacity
Minnesota Living with Heart Failure Quality of Life Questionnaire12 +/- 2 weeksQualitative analysis of quality of life
Stratification by Type II Diabetes Mellitus12 +/- 2 weeksAll results will be stratified by the pre-existing diagnosis of Type II Diabetes Mellitus to determine whether this additional cause of oxidative stress impacts on the ability of inorganic nitrate to recover function in patients with heart failure
Evidence of active dental caries12 +/- 2 weeksPre-specified sub-group analyses by dental disease
Measurement of methaemaglobinaemia12 +/- 2 weeksSafety measure
Contrast Echocardiography: wall stress12 +/- 2 weeksAssessment of left ventricular wall stress
Changes in markers of oxidative stress: oxidised LDL12 +/- 2 weeksMeasured using ELISA and used collectively with MDA and TBAR assays to determine oxidative stress
Changes in markers of oxidative stress: TBAR12 +/- 2 weeksMeasured using ELISA and used collectively with oxidised LDL and MDA assays to determine oxidative stress
Measure of red blood cell XOR activity12 +/- 2 weeksWe will measure expression and activity of XOR by red blood cells, as a marker of both nitrite reductase capacity as well as hyperuricaemia.
Changes in blood pressure12 +/- 2 weeksAnalysis of 24-hour blood pressure monitoring

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026