Raynaud Phenomenon
Conditions
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
Acute and chronic supplementation of beetroot juice.
Sponsors
Study design
Masking description
Double blind, randomised control trial. Supplements will be dispensed by nurses or a member of the research team.
Eligibility
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
| Measure | Time frame | Description |
|---|---|---|
| Peripheral Blood Flow | Baseline (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
| Measure | Time frame | Description |
|---|---|---|
| Overall Number of Participants Recruited | From start of study recruitment until the last participant is randomised. Estimated assesment period 6 - 52 weeks | Number of participants who remained in the study |
| Perceived Pain | Baseline (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 Discomfort | Baseline (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 Rates | From date of randomization until the end of the last study visit. Estimated assesment period 6 - 52 weeks | Establish retention rates (Descriptive statistics) |
| Feasible to Participants | During 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 Participants | During 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
| Arm | Count |
|---|---|
| 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 |
| Total | 23 |
Baseline characteristics
| Characteristic | Nitrate Depleted Beetroot Juice, Then, Beetroot Juice | Total | Beetroot Juice, Then, Nitrate Depleted Beetroot Juice |
|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 8 Participants | 15 Participants | 7 Participants |
| Age, Categorical Between 18 and 65 years | 4 Participants | 8 Participants | 4 Participants |
| Age, Continuous | 63.0 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 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 0 Participants | 1 Participants | 1 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 12 Participants | 22 Participants | 10 Participants |
| Region of Enrollment United Kingdom | 12 Participants | 23 Participants | 11 Participants |
| Sex: Female, Male Female | 11 Participants | 19 Participants | 8 Participants |
| Sex: Female, Male Male | 1 Participants | 4 Participants | 3 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 26 | 0 / 26 |
| other Total, other adverse events | 3 / 26 | 2 / 26 |
| serious Total, serious adverse events | 0 / 26 | 0 / 26 |
Outcome results
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).
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Concentrated Beetroot Juice | Peripheral Blood Flow | Baseline (day 1) | 3.7 flux.mmHg-1 | Standard Deviation 0.4 |
| Concentrated Beetroot Juice | Peripheral Blood Flow | Acute (2 or 23) | 4.1 flux.mmHg-1 | Standard Deviation 0.3 |
| Concentrated Beetroot Juice | Peripheral Blood Flow | Chronic (day 16 or 36) | 4.7 flux.mmHg-1 | Standard Deviation 0.4 |
| Nitrate Depleted Beetroot Juice | Peripheral Blood Flow | Baseline (day 1) | 3.7 flux.mmHg-1 | Standard Deviation 0.4 |
| Nitrate Depleted Beetroot Juice | Peripheral Blood Flow | Acute (2 or 23) | 3.7 flux.mmHg-1 | Standard Deviation 0.3 |
| Nitrate Depleted Beetroot Juice | Peripheral Blood Flow | Chronic (day 16 or 36) | 5.2 flux.mmHg-1 | Standard Deviation 0.4 |
Skin Temperature.
Skin temperature (via thermal imaging).
Time frame: Baseline (day 1), Acute (2 or 23), Chronic (day 16 or 36).
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Concentrated Beetroot Juice | Skin Temperature. | Chronic (day 16 or 36) | 32.2 Degree Celsius | Standard Deviation 3.4 |
| Concentrated Beetroot Juice | Skin Temperature. | Baseline (day 1) | 32.4 Degree Celsius | Standard Deviation 3 |
| Concentrated Beetroot Juice | Skin Temperature. | Acute (day 2 or 23) | 32.1 Degree Celsius | Standard Deviation 2.9 |
| Nitrate Depleted Beetroot Juice | Skin Temperature. | Baseline (day 1) | 32.4 Degree Celsius | Standard Deviation 3 |
| Nitrate Depleted Beetroot Juice | Skin Temperature. | Acute (day 2 or 23) | 32.0 Degree Celsius | Standard Deviation 3 |
| Nitrate Depleted Beetroot Juice | Skin Temperature. | Chronic (day 16 or 36) | 32.4 Degree Celsius | Standard Deviation 2.9 |
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).
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Concentrated Beetroot Juice | Acceptability to Participants | 10 Participants |
| Nitrate Depleted Beetroot Juice | Acceptability to Participants | 10 Participants |
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
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Concentrated Beetroot Juice | Establish Retention Rates | 23 Participants |
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.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Concentrated Beetroot Juice | Feasible to Participants | 10 Participants |
| Nitrate Depleted Beetroot Juice | Feasible to Participants | 10 Participants |
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
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Concentrated Beetroot Juice | Overall Number of Participants Recruited | 23 Participants |
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).
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Concentrated Beetroot Juice | Perceived Discomfort | Baseline (day 1) | 13.4 score on a scale | Standard Deviation 3.8 |
| Concentrated Beetroot Juice | Perceived Discomfort | Acute (day 2 or 23) | 13.1 score on a scale | Standard Deviation 3.2 |
| Concentrated Beetroot Juice | Perceived Discomfort | Chronic (day 16 or 36) | 13.5 score on a scale | Standard Deviation 3.5 |
| Nitrate Depleted Beetroot Juice | Perceived Discomfort | Baseline (day 1) | 13.4 score on a scale | Standard Deviation 3.8 |
| Nitrate Depleted Beetroot Juice | Perceived Discomfort | Acute (day 2 or 23) | 12.6 score on a scale | Standard Deviation 3.7 |
| Nitrate Depleted Beetroot Juice | Perceived Discomfort | Chronic (day 16 or 36) | 12.9 score on a scale | Standard Deviation 3 |
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).
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Concentrated Beetroot Juice | Perceived Pain | Chronic (day 16 or 36) | 0.2 score on a scale | Standard Deviation 0.6 |
| Concentrated Beetroot Juice | Perceived Pain | Baseline (day 1) | 0.2 score on a scale | Standard Deviation 0.6 |
| Concentrated Beetroot Juice | Perceived Pain | Acute (day 2 or 23) | 0.3 score on a scale | Standard Deviation 0.8 |
| Nitrate Depleted Beetroot Juice | Perceived Pain | Chronic (day 16 or 36) | 0.9 score on a scale | Standard Deviation 2.7 |
| Nitrate Depleted Beetroot Juice | Perceived Pain | Baseline (day 1) | 0.2 score on a scale | Standard Deviation 0.6 |
| Nitrate Depleted Beetroot Juice | Perceived Pain | Acute (day 2 or 23) | 0.2 score on a scale | Standard Deviation 0.6 |