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Beet the Cold: The Effect of Inorganic Nitrate Supplementation in Individuals With Raynaud's Phenomenon

Beet the Cold: The Effect of Inorganic Nitrate Supplementation on Peripheral Blood Flow and Pain in Individuals With Raynaud's Phenomenon. A Pilot, Double-blind, Placebo Controlled, Randomised Crossover Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03129178
Enrollment
27
Registered
2017-04-26
Start date
2017-07-01
Completion date
2018-10-01
Last updated
2020-02-10

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

Conditions

Raynaud Phenomenon

Keywords

Nitrate, Nitric oxide, Microvascular

Brief summary

Individuals with Raynaud's phenomenon often experience episodes of reduced blood flow to their fingers and toes during times of stress or cold exposure, causing significant discomfort and pain. Typically, treatment for these individuals involves using drugs like Glyceryl Trinitrate (GTN), which increases blood flow to the fingers and toes by increasing a substance called nitric oxide in the blood. Unfortunately, repeated use of these drugs increases tolerance to them, meaning higher doses are required to produce the same effect. However, increasing the dose can cause more side effects like headaches, and is therefore not considered an ideal long-term therapy. Leafy green vegetables, especially beetroot, contain high amounts of nitrate and are beneficial to blood vessel health, since nitrate from the diet can also be turned into the important blood vessel relaxer, nitric oxide. Unlike GTN, people don't appear to develop a tolerance to dietary nitrate or experience negative side effects. Therefore, this study aims to see if short and longer term beetroot juice supplementation can improve blood flow to the hands and feet in individuals with Raynaud's phenomenon, as well as reduce their pain. This study will tell us how many people are needed for a definitive trial investigating whether beetroot juice can help treat Raynaud's phenomenon. Raynaud's phenomenon can cause significant discomfort and pain to individuals. Dietary nitrate appears to offer a simple, low cost means of improving blood flow to the hands and feet which should reduce both the discomfort and pain experienced characterising this condition. This study will advance our understanding of the causes of Raynaud's phenomenon, specifically the role that the nitrate-nitrite-nitric oxide pathway might play in changing Raynaud's phenomenon symptoms and identifying targets for intervention.

Detailed description

Raynaud's phenomenon (RP) is characterised by a recurrent transient vasospasm of the fingers or toes in response to a cold or stressful stimulus. Nitric oxide (NO•) is a known vasodilator and NO• donors, such as Glyceryl Trinitrate (GTN), improve blood flow in patients with RP and in cold sensitive individuals (Figure 1, see accompanying document). However, individuals develop a tolerance to GTN and show diminishing vasodilatory effects with chronic treatment. In addition, the deleterious side effects such as headaches means that organic nitrates (i.e. GTN and isosorbide mononitrate) are not optimal longterm therapies for RP. Alternative treatments therefore, warrant further investigation. Diets rich in fruit and vegetables has been shown to be effective in reducing blood pressure. In addition, it lowers the risk of morbidity and mortality from cardiovascular disease and are thought to be beneficial to cardiovascular health due to their vasodilatory effects. As diet exhibits such tremendous intra- and inter-individual variation, elucidating which components of such a diet are responsible for this effect is difficult. There is a growing weight of evidence from both human and animal studies that nitrate and nitrite derived from the diet can serve as a source for nitric oxide (NO; please see below), particularly where it is deficient. Indeed, the greatest protective effect on cardiovascular disease is to be found in those diets with the greatest consumption of green leafy and or cruciferous vegetables which typically have high nitrate content. NO is produced in the body in two ways. The first requires the availability the amino acid L-arginine, molecular oxygen, and families of enzymes, the nitric oxide synthases (NOS); that is the NOS pathway. The second pathway is independent of NOS pathway and involves the stepwise enzymatic and chemical reduction of inorganic nitrate to nitrite. A major source of nitrite in humans is the reduction of dietary nitrate by facultative anaerobic bacteria in the mouth. The remaining nitrite is then absorbed into the circulation where it acts as a storage pool for subsequent NO• production, which is expedited in hypoxaemia. Localised hypoxemia such as that observed in the digital vasculature of individuals with RP is a potential therapeutic target for dietary nitrate supplementation. In contrast to organic nitrates (GTN), inorganic nitrate (in the form of beetroot juice) does not cause the same negative side effects or demonstrate tachyphylaxis whilst it does notable improve skin blood flow, microvascular function and lower blood pressure (BP) in healthy individuals and chronic conditions such as hypertension, peripheral arterial disease, heart failure and chronic obstructive pulmonary disease. Thus concentrated beetroot juice (CBJ) may offer an inexpensive, safe and potentially effective intervention to improve the pain and reduced peripheral blood flow characterising individuals with RP. RP can cause significant discomfort and pain to individuals during a vasospasm. Dietary nitrate appears to offer a simple, low cost means of modifying blood flow to the peripheries and, ultimately, reducing both the discomfort and pain experienced by individuals with RP. This study will also advance our understanding of the aetiology and pathophysiology of RP, specifically the role that the nitrate-nitrite-nitric oxide pathway might play in modulating RP symptoms. An understanding of the effects of concentrated beetroot juice on microvascular blood flow and pain may lead to a range of simple, low cost and effective therapeutic interventions to prevent and treat episodes of RP.

Interventions

DIETARY_SUPPLEMENTConcentrated beetroot juice

Acute and chronic supplementation of beetroot juice.

Sponsors

Loughborough University
CollaboratorOTHER
University of Exeter
CollaboratorOTHER
University of Portsmouth
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

Double blind, randomised control trial. Supplements will be dispensed by nurses or a member of the research team.

Eligibility

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

Inclusion criteria

* Male or Female, aged 18 years or above. * Diagnosed with Raynaud's Phenomenon. * Participant is willing and able to give informed consent for participation in the study.

Exclusion criteria

The participant may not enter the study if ANY of the following apply: * Patients with significant renal impairment (eGFR\<30) * Uncontrolled hypertension, * Taking regular organic nitrates, nicorandil, or thiazolidinidiones, * or any medication which may interfere with data interpretation or safety, * who have had a myocardial infarction or cerebro-vascular event, * who smoke, * or any other serious medical condition which would interfere with data interpretation or safety will be excluded from participation.

Design outcomes

Primary

MeasureTime frameDescription
Peripheral Blood FlowBaseline (day 1), Acute (2 or 23), Chronic (day 16 or 36).Peripheral blood flow (CVC = skin flux/MAP; flux.mmHg-1).
Skin Temperature.Baseline (day 1), Acute (2 or 23), Chronic (day 16 or 36).Skin temperature (via thermal imaging).

Secondary

MeasureTime frameDescription
Overall Number of Participants RecruitedFrom start of study recruitment until the last participant is randomised. Estimated assesment period 6 - 52 weeksNumber of participants who remained in the study
Perceived PainBaseline (day 1), Acute (2 or 23), Chronic (day 16 or 36).Perceived pain. Pain sensation was assessed using a numerical rating scale for pain (0 no pain, 10 unimaginable, unspeakable pain; (Ferreira-Valente et al., 2011)) at the same time points.
Perceived DiscomfortBaseline (day 1), Acute (2 or 23), Chronic (day 16 or 36).Perceived discomfort. Thermal discomfort were measured using a 20 cm scale (0 = very cold/uncomfortable; 10 = neutral; 20 = very hot/comfortable; modified from Zhang et al. (2004)) and recorded prior to immersion, during immersion and every 2 minutes of the rewarming period.
Establish Retention RatesFrom date of randomization until the end of the last study visit. Estimated assesment period 6 - 52 weeksEstablish retention rates (Descriptive statistics)
Feasible to ParticipantsDuring qualitative interviews after the intervention has ended (post day 36).Feasible to participants via interview. Specifically, semi-structured interviews explored participants' experiences of the study procedures and consumption of beetroot juice. Interviews were conducted by a researcher with experience in qualitative research methods. Interviews were recorded, transcribed verbatim, and analysed through thematic analysis as outlined by Braun and Clarke (2006).
Acceptability to ParticipantsDuring qualitative interviews after the intervention has ended (post day 36).Interview. Specifically, semi-structured interviews explored participants' experiences of the study procedures and consumption of beetroot juice. Interviews were conducted by a researcher with experience in qualitative research methods. Interviews were recorded, transcribed verbatim, and analysed through thematic analysis as outlined by Braun and Clarke (2006). Participants were asked about the testing procedures and their thoughts on the juice.

Countries

United Kingdom

Participant flow

Recruitment details

96 people were assessed for eligibility from clinic letters, word of mouth, local groups and via the clinical trials website. Recruitment occurred from 06-07-2017 - 29-05-2018.

Pre-assignment details

27 participants were consented.

Participants by arm

ArmCount
Beetroot Juice, Then, Nitrate Depleted Beetroot Juice
Participants consumed 140ml of beetroot juice prior to their first experimental visit. Participants will then be asked to consume 70ml a day for 2 weeks and final visit the investigators once more following another 140ml drink. Following a 7 day washout, then swapped into the nitrate depleted beetroot juice arm.
11
Nitrate Depleted Beetroot Juice, Then, Beetroot Juice
Participants consumed 140ml of nitrate depleted beetroot juice prior to their first experimental visit. Participants will then be asked to consume 70ml a day for 2 weeks and final visit the investigators once more following another 140ml drink. Following a 7 day washout, then swapped into the beetroot juice arm.
12
Total23

Baseline characteristics

CharacteristicNitrate Depleted Beetroot Juice, Then, Beetroot JuiceTotalBeetroot Juice, Then, Nitrate Depleted Beetroot Juice
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
8 Participants15 Participants7 Participants
Age, Categorical
Between 18 and 65 years
4 Participants8 Participants4 Participants
Age, Continuous63.0 years
STANDARD_DEVIATION 15.2
64.3 years
STANDARD_DEVIATION 15.3
65.7 years
STANDARD_DEVIATION 16
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
0 Participants1 Participants1 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
12 Participants22 Participants10 Participants
Region of Enrollment
United Kingdom
12 Participants23 Participants11 Participants
Sex: Female, Male
Female
11 Participants19 Participants8 Participants
Sex: Female, Male
Male
1 Participants4 Participants3 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 260 / 26
other
Total, other adverse events
3 / 262 / 26
serious
Total, serious adverse events
0 / 260 / 26

Outcome results

Primary

Peripheral Blood Flow

Peripheral blood flow (CVC = skin flux/MAP; flux.mmHg-1).

Time frame: Baseline (day 1), Acute (2 or 23), Chronic (day 16 or 36).

Population: 20 individuals with raynauds phenomenon. Result reported is Blood flow (CVC), 10 minutes after rewarming for the chronic exposures (Baseline (day 1), visit 2 (day 2), 3 (day 16), 4 (day 23) and 5 (day 36) respectfully).

ArmMeasureGroupValue (MEAN)Dispersion
Concentrated Beetroot JuicePeripheral Blood FlowBaseline (day 1)3.7 flux.mmHg-1Standard Deviation 0.4
Concentrated Beetroot JuicePeripheral Blood FlowAcute (2 or 23)4.1 flux.mmHg-1Standard Deviation 0.3
Concentrated Beetroot JuicePeripheral Blood FlowChronic (day 16 or 36)4.7 flux.mmHg-1Standard Deviation 0.4
Nitrate Depleted Beetroot JuicePeripheral Blood FlowBaseline (day 1)3.7 flux.mmHg-1Standard Deviation 0.4
Nitrate Depleted Beetroot JuicePeripheral Blood FlowAcute (2 or 23)3.7 flux.mmHg-1Standard Deviation 0.3
Nitrate Depleted Beetroot JuicePeripheral Blood FlowChronic (day 16 or 36)5.2 flux.mmHg-1Standard Deviation 0.4
Primary

Skin Temperature.

Skin temperature (via thermal imaging).

Time frame: Baseline (day 1), Acute (2 or 23), Chronic (day 16 or 36).

ArmMeasureGroupValue (MEAN)Dispersion
Concentrated Beetroot JuiceSkin Temperature.Chronic (day 16 or 36)32.2 Degree CelsiusStandard Deviation 3.4
Concentrated Beetroot JuiceSkin Temperature.Baseline (day 1)32.4 Degree CelsiusStandard Deviation 3
Concentrated Beetroot JuiceSkin Temperature.Acute (day 2 or 23)32.1 Degree CelsiusStandard Deviation 2.9
Nitrate Depleted Beetroot JuiceSkin Temperature.Baseline (day 1)32.4 Degree CelsiusStandard Deviation 3
Nitrate Depleted Beetroot JuiceSkin Temperature.Acute (day 2 or 23)32.0 Degree CelsiusStandard Deviation 3
Nitrate Depleted Beetroot JuiceSkin Temperature.Chronic (day 16 or 36)32.4 Degree CelsiusStandard Deviation 2.9
Secondary

Acceptability to Participants

Interview. Specifically, semi-structured interviews explored participants' experiences of the study procedures and consumption of beetroot juice. Interviews were conducted by a researcher with experience in qualitative research methods. Interviews were recorded, transcribed verbatim, and analysed through thematic analysis as outlined by Braun and Clarke (2006). Participants were asked about the testing procedures and their thoughts on the juice.

Time frame: During qualitative interviews after the intervention has ended (post day 36).

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Concentrated Beetroot JuiceAcceptability to Participants10 Participants
Nitrate Depleted Beetroot JuiceAcceptability to Participants10 Participants
Secondary

Establish Retention Rates

Establish retention rates (Descriptive statistics)

Time frame: From date of randomization until the end of the last study visit. Estimated assesment period 6 - 52 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Concentrated Beetroot JuiceEstablish Retention Rates23 Participants
Secondary

Feasible to Participants

Feasible to participants via interview. Specifically, semi-structured interviews explored participants' experiences of the study procedures and consumption of beetroot juice. Interviews were conducted by a researcher with experience in qualitative research methods. Interviews were recorded, transcribed verbatim, and analysed through thematic analysis as outlined by Braun and Clarke (2006).

Time frame: During qualitative interviews after the intervention has ended (post day 36).

Population: Qualitative outcome.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Concentrated Beetroot JuiceFeasible to Participants10 Participants
Nitrate Depleted Beetroot JuiceFeasible to Participants10 Participants
Secondary

Overall Number of Participants Recruited

Number of participants who remained in the study

Time frame: From start of study recruitment until the last participant is randomised. Estimated assesment period 6 - 52 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Concentrated Beetroot JuiceOverall Number of Participants Recruited23 Participants
Secondary

Perceived Discomfort

Perceived discomfort. Thermal discomfort were measured using a 20 cm scale (0 = very cold/uncomfortable; 10 = neutral; 20 = very hot/comfortable; modified from Zhang et al. (2004)) and recorded prior to immersion, during immersion and every 2 minutes of the rewarming period.

Time frame: Baseline (day 1), Acute (2 or 23), Chronic (day 16 or 36).

ArmMeasureGroupValue (MEAN)Dispersion
Concentrated Beetroot JuicePerceived DiscomfortBaseline (day 1)13.4 score on a scaleStandard Deviation 3.8
Concentrated Beetroot JuicePerceived DiscomfortAcute (day 2 or 23)13.1 score on a scaleStandard Deviation 3.2
Concentrated Beetroot JuicePerceived DiscomfortChronic (day 16 or 36)13.5 score on a scaleStandard Deviation 3.5
Nitrate Depleted Beetroot JuicePerceived DiscomfortBaseline (day 1)13.4 score on a scaleStandard Deviation 3.8
Nitrate Depleted Beetroot JuicePerceived DiscomfortAcute (day 2 or 23)12.6 score on a scaleStandard Deviation 3.7
Nitrate Depleted Beetroot JuicePerceived DiscomfortChronic (day 16 or 36)12.9 score on a scaleStandard Deviation 3
Secondary

Perceived Pain

Perceived pain. Pain sensation was assessed using a numerical rating scale for pain (0 no pain, 10 unimaginable, unspeakable pain; (Ferreira-Valente et al., 2011)) at the same time points.

Time frame: Baseline (day 1), Acute (2 or 23), Chronic (day 16 or 36).

ArmMeasureGroupValue (MEAN)Dispersion
Concentrated Beetroot JuicePerceived PainChronic (day 16 or 36)0.2 score on a scaleStandard Deviation 0.6
Concentrated Beetroot JuicePerceived PainBaseline (day 1)0.2 score on a scaleStandard Deviation 0.6
Concentrated Beetroot JuicePerceived PainAcute (day 2 or 23)0.3 score on a scaleStandard Deviation 0.8
Nitrate Depleted Beetroot JuicePerceived PainChronic (day 16 or 36)0.9 score on a scaleStandard Deviation 2.7
Nitrate Depleted Beetroot JuicePerceived PainBaseline (day 1)0.2 score on a scaleStandard Deviation 0.6
Nitrate Depleted Beetroot JuicePerceived PainAcute (day 2 or 23)0.2 score on a scaleStandard Deviation 0.6

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