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Dietary Nitrate Supplementation and Thermoregulation

Dietary Nitrate Supplementation and Thermoregulation During Exercise

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03506646
Enrollment
11
Registered
2018-04-24
Start date
2018-09-05
Completion date
2022-12-15
Last updated
2024-11-22

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

Conditions

Peripheral Arterial Disease, Peripheral Artery Disease

Brief summary

This is a double-blinded, randomized, crossover design study to assess the effects of dietary nitrate supplementation (beetroot juice) on peripheral artery disease (PAD) patients (ages 50-85) diagnosed with Fontaine stage I or II PAD (as determined by vascular surgeon at UNMC). Exclusion criteria include: 1) experience severe claudication (leg pain) at rest or tissue loss due to PAD (Fontaine stage III and IV), 2) have limited walking capacity due to conditions other than PAD, 3) are already supplementing with a form of dietary nitrate, or 4) have an allergy to beetroot juice. Subjects will be required to visit the lab 3 times and will be randomized to receive either the supplement or the placebo for the 2nd and 3rd visits. There will be a washout period of 14 days between the 2nd and 3rd visits. Visit 1 will take approximately 2 hours and the 2nd/3rd visits will take approximately 1.5 hours. Total experimentation period will last approximately 15 days. Visit 1 will consist of non-invasive baseline testing including assessment of endothelial function (flow-mediated dilation by ultrasound imaging), maximal walking capacity (Gardner treadmill protocol), leg function (near-infrared spectroscopy, time to onset claudication, blood flow to lower extremities), and body core temperature (rectal thermometer). Visits 2 and 3 will require consumption of either the supplement or placebo. The same tests from the baseline measurements will be performed for visits 2 and 3. There will be a recommended fourth visit, albeit not required, to review study results.

Detailed description

Background and rationale The vast majority of the research involving dietary nitrate supplementation, namely beetroot juice, has been performed mostly on samples of healthy populations. A few clinical populations have been studied, including heart failure with preserved ejection fraction, chronic obstructive pulmonary disease (COPD), and peripheral artery disease (PAD). In various populations, beetroot juice (BRJ) has been shown to decrease overall blood pressure, increase blood flow, increase muscle tissue oxygenation, improve body core temperature regulation, and increase exercise tolerance while decreasing the oxygen cost of exercise. Blood pressure BRJ supplementation has been shown to have an immediate effect on reducing blood pressure, with the most substantial decreases recorded within approximately 2.5-3 hours following supplement consumption \[1, 2\]. Systolic, diastolic, and mean arterial blood pressures showed decreases of 10.4±3 mmHg, 8.1±2.1 mmHg, and 8.0±2.1 mmHg, respectively, in healthy volunteers \[2\]. During exercise in healthy individuals, systolic blood pressure remained lower throughout varying exercise intensities \[1\]. Blood pressure was also reduced in heart failure with preserved ejection fraction patients. After an acute dose of BRJ, resting systolic blood pressure significantly decreased when compared to placebo conditions (BRJ 127 ± 14 mmHg; placebo134 ± 14 mmHg) \[3\]. A slight reduction in systolic blood pressure during exercise may be beneficial to PAD patients. Hypertension, or high blood pressure, is a major risk factor for the development of PAD \[4\]. Decreasing overall blood pressure and slightly decreasing systolic blood pressure in response to light activity would result in a decrease in unnecessary stress placed on the cardiovascular system at rest and during exercise. In a study involving PAD patients where 7 of the 8 participants were classified as either hypertensive or prehypertensive, BRJ consumption caused a significant reduction in diastolic blood pressure during rest that was maintained during exercise testing \[5\]. The study concludes that their data suggest that BRJ supplementation reduces blood pressure in PAD patients and this effect is maintained throughout exercise \[5\]. Oxygen delivery and muscle tissue oxygenation Oxygen demand of working muscle increases as activity level increases the efficiency of oxygen delivery and oxygen utilization is crucial to muscle function, as well as a necessary increase in blood flow. This is especially important in PAD patients; increasing oxygenation to areas of skeletal muscle ischemia may increase physical function. By using near-infrared spectroscopy, muscle tissue oxygenation can be examined. During cycling in healthy males supplementing with BRJ, the right vastus lateralis muscle oxyhemoglobin concentrations were greater than that of the placebo condition \[6\]. While cycling at a moderate intensity, the male cyclists had a 13% reduction in deoxyhemoglobin concentration amplitude post-supplementation, which indicated a reduction in fractional oxygen extraction in the right vastus lateralis muscle \[6\]. These results suggest that BRJ supplementation may promote a better balance between localized oxygen delivery and utilization as an index of muscle fractional oxygen extraction \[6\]. Overall, BRJ supplementation has been shown to increase working muscle tissue oxygenation during exercise. In PAD patients, the oxygenation of the gastrocnemius with the worst PAD symptoms was monitored during a walking cardiopulmonary exercise test. Subjects showed a 48% reduction in deoxyhemoglobin concentration amplitude following BRJ supplementation, which indicated that fractional oxygen extraction was reduced \[5\]. During the exercise protocol, deoxyhemoglobin amplitude measures for the BRJ supplementation group at 100 and 200 seconds into exercise were reduced by 44% and 53%, respectively \[5\]. This response implies that BRJ supplementation in PAD patients improves a balance between local oxygen delivery and utilization as an index of muscle fractional oxygenation extraction by the working muscle. Increasing oxygenation to areas of skeletal muscle ischemia in PAD patients may increase physical function, but in order for this to be as efficient as possible, a dose-response relationship must be determined. Blood flow and thermoregulatory response Increases in activity and oxygen demand of working skeletal muscle necessitate increases in blood flow. In PAD patients, increasing blood flow to working muscle becomes difficult due to atherosclerotic occlusions in the lower extremity arteries. Research in healthy populations showed significant increases in forearm blood flow during hand grip exercise in hypoxic conditions following an acute dosage of BRJ in comparison to placebo (BRJ 373 ± 38 mL/min; placebo 343 ± 32 mL/min). Nitric oxide signals smooth muscle within the blood vessels (endothelium) to relax, which in turn increases blood flow to the localized area of vasodilation. In healthy populations, dietary nitrate supplementation increases vasodilation near the surface of the skin \[7\]. This increase in vasodilatory capacity and blood flow would create a stronger temperature gradient at the level of the skin, which would facilitate more efficient heat exchange as blood is cooled at the level of the skin (sweat evaporative, conductive, and convective cooling), causing decreased strain on the body. In PAD patients, nitrite-related nitric oxide signaling showed to increase peripheral blood flow to hypoxic tissue, which is supported by a decrease in gastrocnemius deoxygenation and a decrease in blood pressure \[5\]. However, during brachial artery flow mediated dilation, peak dilation did not significantly change (BRJ 42.6 ± 10.6 seconds; placebo 41.0 ± 10.39 seconds), which suggested that endothelial production of nitric oxide did not change \[5\]. The unchanging vasodilatory response is likely due to the study not examining a BRJ dose-response relationship and its effects on vasodilation. Exercise tolerance and oxygen cost BRJ supplementation has been shown to decrease oxygen cost during low-intensity and moderate-intensity exercise. In trained populations supplementing with BRJ, significant decreases in oxygen cost during the beginning stages of exercise have been detected \[8, 9\]. Oxygen cost during walking was shown to decrease by approximately 12% following BRJ supplementation \[8\]. BRJ supplementation showed a 20% decrease in oxygen cost during moderate-intensity cycling in recreationally trained men \[10\]. This reduction in oxygen cost implies an increase in exercise efficiency in light-to-moderate level exercise, which in turn increases exercise tolerance. In high-intensity exercise, time-to-exercise-failure increased by 15% following BRJ supplementation, which is also suggestive of an increase in exercise tolerance \[8\]. BRJ supplementation in clinical populations has also shown to improve exercise tolerance. In heart failure with preserved ejection fraction patients, submaximal endurance exercise improved by 24% following BRJ supplementation in comparison to placebo conditions (BRJ 449 ± 180 seconds; placebo 363 ± 125 seconds) \[3\]. In patients with COPD, walking distance increased by 11% and time to exercise fatigue increased by 6% \[11\]. In PAD patients, BRJ supplementation showed an 18% (32 second) increase to onset claudication pain and a 17% (65 seconds) increase peak walking time in comparison to placebo conditions \[5\]. These results in PAD patients show a substantial acute response to BRJ supplementation (\ 2 hours of consumption) during exercise testing. In various populations, BRJ supplementation has shown to decrease blood pressure, improve blood flow, increase muscle tissue oxygenation, safely maintain core temperature, and increase exercise tolerance. The effects of BRJ specifically in PAD patients showed decreases in blood pressure, increases in time to onset claudication and exercise tolerance, but did not show a significant effect on endothelial function. Examining a dose-response relationship is necessary to determine the responses to BRJ supplementation (endothelial function, leg function, and blood vessel oxygen carrying capacity) in PAD patients.In this study, a higher dose of nitrate (280 mL, 16.8 mmol nitrates) will be examined \[12\]. BRJ supplementation has shown reductions in blood pressure, increased muscle tissue oxygenation, blood flow, and thermoregulatory response. These mechanisms all contribute to improving overall cardiovascular function. If these results are observed during this study, PAD patients may experience less claudication pain as well as better tolerance to daily physical activities and exercise.

Interventions

DIETARY_SUPPLEMENTPlacebo

Participants will be given a gelatin tablet to serve as the control condition. This will be a double-blinded, randomized, cross-over design to examine the effects of beetroot juice on endothelial function, leg function, and thermoregulation.

DIETARY_SUPPLEMENTBeet root juice

Beet root juice serves as a mode of dietary nitrate supplementation. This will be a double-blinded, randomized, cross-over design to examine the effects of beetroot juice on endothelial function, leg function, and thermoregulation.

Sponsors

University of Nebraska
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Intervention model description

1:1 randomized, cross-over, double-blinded

Eligibility

Sex/Gender
ALL
Age
50 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

1. be able to give written, informed consent 2. demonstrate positive history of chronic claudication 3. have a history of exercise-limiting claudication 4. have an ankle/brachial index \< 0.90 at rest 5. have a stable blood pressure regimen, stable lipid regimen, stable diabetes regimen and risk factor control for 6 weeks. 6. be between 50-85 years old

Exclusion criteria

1. pain at rest (severe claudication) and/or tissue loss due to PAD (Fontaine stage III and IV) 2. acute lower extremity ischemic event secondary to thromboembolic disease or acute trauma 3. limited walking capacity due to other conditions other than PAD 4. a form of nitrate supplementation already included in their diet/regimen 5. an allergy to beetroot juice

Design outcomes

Primary

MeasureTime frameDescription
Brachial Artery Endothelial FunctionPre and post treatmentEndothelial function will be assessed using flow mediated dilation to measure vasodilation in the brachial artery (baFMD).

Secondary

MeasureTime frameDescription
Muscle Tissue Oxygenation2 daysMuscle tissue oxygenation will be assessed by using near-infrared spectroscopy (NIRS) during a maximal walking protocol. Assessment is measured in arbitrary units as mean changes in deoxygenated hemoglobin (HHb)
Physical Walking Capacitymaximum of 14 minutes each day for 2 daysPhysical walking capacity will be measured during the Gardner treadmill protocol. Participants will walk on a treadmill at 2.0 mph. Grade will began at zero and will be increased by two percent every two minutes. Participants unable to walk at least 2.0 miles per hour (MPH) begin walking at 0.5 MPH and their speed is increased by 0.50 MPH every two minutes until the participant reaches 2.0 MPH. After reaching 2.0 MPH, treadmill grade is increased by two percent every two minutes. Participants are asked to continue walking without stopping until they cannot continue because of leg symptoms, exhaustion, or other symptoms.
Leg Endothelial FunctionPre and Post treatmentPopliteal artery endothelial function will be measured using the flow mediated dilation (paFMD) technique to measure vasodilation with an ultrasound imaging system.
Microvascular Functionmaximum of 30 minutes each day for 2 daysMicrovascular function will be assessed using near-infrared spectroscopy. Changes in tissue oxygenation rate following reactive hyperemia will be denoted as % recovery rate used to interpret mitochondrial function.
Blood Nitrate/Nitrite Levels2 daysParticipants will have blood drawn from an antecubital vein using a vacutainer and needle (25 gauge) prior to baseline testing and experimental trial testing. This will be done to measure nitrate/nitrite levels at baseline, post beetroot juice (BRJ) intake, and post placebo intake.
Autonomic Nervous System Activitymaximum of 60 minutes each day for 2 daysAutonomic nervous system activity will be assessed using heart rate variability. Data represented as ratio between low frequency (LF) and high frequency (HF).

Countries

United States

Participant flow

Participants by arm

ArmCount
Beetroot Juice First, Then Placebo
Subjects will be tested on two different days. The first day will be beetroot juice and the second day will be a placebo. Testing will take place approximately one hour after intake. There will be a 14 day washout period between testing days. Beetroot juice: Beetroot juice serves as a mode of dietary nitrate supplementation. This will be a double-blinded, randomized, cross-over design to examine the effects of beetroot juice on endothelial function, leg function, and thermoregulation.
6
Placebo First, Then Beetroot Juice
Subjects will be tested on two different days. The first day will be a placebo and the second day will be beetroot juice. Testing will take place approximately one hour after intake. There will be a 14 day washout period between testing days. Beetroot juice: Beetroot juice serves as a mode of dietary nitrate supplementation. This will be a double-blinded, randomized, cross-over design to examine the effects of beetroot juice on endothelial function, leg function, and thermoregulation.
5
Total11

Baseline characteristics

CharacteristicBeetroot Juice First, Then PlaceboPlacebo First, Then Beetroot JuiceTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
4 Participants4 Participants8 Participants
Age, Categorical
Between 18 and 65 years
2 Participants1 Participants3 Participants
Age, Continuous69.5 years
STANDARD_DEVIATION 7.26
70.80 years
STANDARD_DEVIATION 10.28
70.1 years
STANDARD_DEVIATION 8.3
Body fat percentage39 % body fat
STANDARD_DEVIATION 10.22
35.7 % body fat
STANDARD_DEVIATION 8.08
37.35 % body fat
STANDARD_DEVIATION 9.15
Hand grip strength29.33 kg
STANDARD_DEVIATION 14.75
29.60 kg
STANDARD_DEVIATION 8.65
29.47 kg
STANDARD_DEVIATION 11.7
Height165.92 cm
STANDARD_DEVIATION 16.1
160 cm
STANDARD_DEVIATION 11.77
162.96 cm
STANDARD_DEVIATION 13.94
Race and Ethnicity Not Collected0 Participants
Region of Enrollment
United States
6 participants5 participants11 participants
Resting Blood Pressure
Diastolic blood pressure
82 mm/Hg
STANDARD_DEVIATION 7
79 mm/Hg
STANDARD_DEVIATION 5
80 mm/Hg
STANDARD_DEVIATION 6
Resting Blood Pressure
Systolic blood pressure
134 mm/Hg
STANDARD_DEVIATION 11
127 mm/Hg
STANDARD_DEVIATION 22
131 mm/Hg
STANDARD_DEVIATION 16
Resting Heart Rate71.2 beats per min
STANDARD_DEVIATION 8.9
68.2 beats per min
STANDARD_DEVIATION 14.5
69.8 beats per min
STANDARD_DEVIATION 11.2
Sex: Female, Male
Female
3 Participants3 Participants6 Participants
Sex: Female, Male
Male
3 Participants2 Participants5 Participants
Weight84.17 kg
STANDARD_DEVIATION 17.34
68.54 kg
STANDARD_DEVIATION 12.57
76.35 kg
STANDARD_DEVIATION 14.95

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 110 / 11
other
Total, other adverse events
0 / 110 / 11
serious
Total, serious adverse events
0 / 110 / 11

Outcome results

Primary

Brachial Artery Endothelial Function

Endothelial function will be assessed using flow mediated dilation to measure vasodilation in the brachial artery (baFMD).

Time frame: Pre and post treatment

Population: 11 patients with peripheral artery disease were recruited and assigned to the beetroot juice and placebo groups in a randomized crossover study design.

ArmMeasureGroupValue (MEAN)Dispersion
Beetroot JuiceBrachial Artery Endothelial FunctionBaseline4.34 % dilationStandard Deviation 1.39
Beetroot JuiceBrachial Artery Endothelial FunctionPost Treatment5.6 % dilationStandard Deviation 1.65
PlaceboBrachial Artery Endothelial FunctionBaseline4.31 % dilationStandard Deviation 1.26
PlaceboBrachial Artery Endothelial FunctionPost Treatment4.35 % dilationStandard Deviation 1.24
Secondary

Autonomic Nervous System Activity

Autonomic nervous system activity will be assessed using heart rate variability. Data represented as ratio between low frequency (LF) and high frequency (HF).

Time frame: maximum of 60 minutes each day for 2 days

ArmMeasureGroupValue (MEAN)Dispersion
Beetroot JuiceAutonomic Nervous System ActivityBaseline2.6 RatioStandard Deviation 0.8
Beetroot JuiceAutonomic Nervous System ActivityPost treatment2.1 RatioStandard Deviation 0.7
PlaceboAutonomic Nervous System ActivityPost treatment2.8 RatioStandard Deviation 0.6
PlaceboAutonomic Nervous System ActivityBaseline2.4 RatioStandard Deviation 0.5
Secondary

Blood Nitrate/Nitrite Levels

Participants will have blood drawn from an antecubital vein using a vacutainer and needle (25 gauge) prior to baseline testing and experimental trial testing. This will be done to measure nitrate/nitrite levels at baseline, post beetroot juice (BRJ) intake, and post placebo intake.

Time frame: 2 days

ArmMeasureGroupValue (MEAN)Dispersion
Beetroot JuiceBlood Nitrate/Nitrite LevelsPre treatment.22 micromolar concentrationStandard Deviation 0.09
Beetroot JuiceBlood Nitrate/Nitrite LevelsPost Treatment1.54 micromolar concentrationStandard Deviation 0.44
PlaceboBlood Nitrate/Nitrite LevelsPre treatment.27 micromolar concentrationStandard Deviation 0.16
PlaceboBlood Nitrate/Nitrite LevelsPost Treatment.25 micromolar concentrationStandard Deviation 0.17
Secondary

Leg Endothelial Function

Popliteal artery endothelial function will be measured using the flow mediated dilation (paFMD) technique to measure vasodilation with an ultrasound imaging system.

Time frame: Pre and Post treatment

Population: 11 patients with peripheral artery disease were recruited and assigned to the beetroot juice and placebo groups in a randomized crossover study design.

ArmMeasureGroupValue (MEAN)Dispersion
Beetroot JuiceLeg Endothelial FunctionBaseline2.45 % dilationStandard Deviation 1.3
Beetroot JuiceLeg Endothelial FunctionPost Treatment4.11 % dilationStandard Deviation 2.12
PlaceboLeg Endothelial FunctionBaseline2.73 % dilationStandard Deviation 1.46
PlaceboLeg Endothelial FunctionPost Treatment2.73 % dilationStandard Deviation 1.46
Secondary

Microvascular Function

Microvascular function will be assessed using near-infrared spectroscopy. Changes in tissue oxygenation rate following reactive hyperemia will be denoted as % recovery rate used to interpret mitochondrial function.

Time frame: maximum of 30 minutes each day for 2 days

ArmMeasureGroupValue (MEAN)Dispersion
Beetroot JuiceMicrovascular FunctionBaseline24.74 % recovery rateStandard Deviation 15.02
Beetroot JuiceMicrovascular FunctionPost treatment46.87 % recovery rateStandard Deviation 18.18
PlaceboMicrovascular FunctionBaseline28.05 % recovery rateStandard Deviation 17.95
PlaceboMicrovascular FunctionPost treatment30.13 % recovery rateStandard Deviation 17.57
Secondary

Muscle Tissue Oxygenation

Muscle tissue oxygenation will be assessed by using near-infrared spectroscopy (NIRS) during a maximal walking protocol. Assessment is measured in arbitrary units as mean changes in deoxygenated hemoglobin (HHb)

Time frame: 2 days

ArmMeasureGroupValue (MEAN)Dispersion
Beetroot JuiceMuscle Tissue OxygenationBaseline7.19 arbitrary unitsStandard Deviation 49.5
Beetroot JuiceMuscle Tissue OxygenationPost Treatment-9.48 arbitrary unitsStandard Deviation 23.2
PlaceboMuscle Tissue OxygenationBaseline1.12 arbitrary unitsStandard Deviation 30.1
PlaceboMuscle Tissue OxygenationPost Treatment3.86 arbitrary unitsStandard Deviation 26.7
Secondary

Physical Walking Capacity

Physical walking capacity will be measured during the Gardner treadmill protocol. Participants will walk on a treadmill at 2.0 mph. Grade will began at zero and will be increased by two percent every two minutes. Participants unable to walk at least 2.0 miles per hour (MPH) begin walking at 0.5 MPH and their speed is increased by 0.50 MPH every two minutes until the participant reaches 2.0 MPH. After reaching 2.0 MPH, treadmill grade is increased by two percent every two minutes. Participants are asked to continue walking without stopping until they cannot continue because of leg symptoms, exhaustion, or other symptoms.

Time frame: maximum of 14 minutes each day for 2 days

ArmMeasureGroupValue (MEAN)Dispersion
Beetroot JuicePhysical Walking CapacityBaseline368.3 metersStandard Deviation 243.3
Beetroot JuicePhysical Walking CapacityPost treatment460.5 metersStandard Deviation 279.3
PlaceboPhysical Walking CapacityBaseline366.1 metersStandard Deviation 245.6
PlaceboPhysical Walking CapacityPost treatment361.8 metersStandard Deviation 262.9

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