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Beetroot Juice and Postprandial Vascular Activity

The Effects of Beetroot Juice on Postprandial Vascular Activity After a High-fat Meal in Overweight and Slightly Obese Men

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01559441
Enrollment
20
Registered
2012-03-21
Start date
2012-03-31
Completion date
2012-08-31
Last updated
2013-07-16

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

Conditions

Dyslipidemia

Keywords

beetroot juice, nitrate, vascular activity, postprandial state

Brief summary

Increased postprandial lipemia may increase the risk for cardiovascular diseases. An important mechanistic link between lipemia following a high-fat meal and adverse cardiovascular events is lipid-mediated endothelial activation. Therefore, it is important to identify nutrients that can neutralize this acute vascular disturbance. The investigators hypothesize that beetroot juice, a food rich in inorganic nitrate, could improve vascular activity during the postprandial phase.

Interventions

DIETARY_SUPPLEMENTBeetroot Juice with oral fat load

140mL (9.6 mmol nitrate) beetroot juice (Beet It, James White drinks Ltd)

DIETARY_SUPPLEMENTCarbohydrate control drink with oral fat load

140 mL (low-nitrate) carbohydrate control drink

Sponsors

Top Institute Food and Nutrition
CollaboratorOTHER
Maastricht University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged between 18 and 70 years * Quetelet-index between 28-35 kg/m2 * Mean serum triacylglycerol ≤1.7 mmol/L * No indication for treatment with cholesterol-lowering drugs according to the Dutch Cholesterol Consensus * No current smoker * No diabetic patients or individuals receiving antidiabetic medication * No familial hypercholesterolemia * No abuse of drugs * Less than 21 alcoholic consumptions per week * Stable body weight (weight gain or loss \<3 kg in the past three months) * No use of medication known to affect serum lipid metabolism * No severe medical conditions that might interfere with the study, such as high blood pressure, epilepsy, asthma, allergies, chronic obstructive pulmonary disease, inflammatory bowel diseases, auto inflammatory diseases and rheumatoid arthritis * No active cardiovascular disease like congestive heart failure or recent (\<6 months) event (acute myocardial infarction, cerebro vascular accident) * Willingness to stop the consumption of foods rich in nitrates 3 weeks before the start of the study. Vegetables such as beets, celery, radishes, turnips and spinach are rich in nitrates * Willingness to give up being a blood donor (or having donated blood) from 8 weeks before the start of the study, during the study and for 4 weeks after completion of the study * No difficult venipuncture as evidenced during the screening visits

Exclusion criteria

* Women * Quetelet-index between \<28 or \>35 kg/m2 * Mean serum triacylglycerol ≥1.7 mmol/L * Indication for treatment with cholesterol-lowering drugs according to the Dutch Cholesterol Consensus * Current smoker * Diabetic patients or individuals receiving antidiabetic medication * Familial hypercholesterolemia * Abuse of drugs * More than 21 alcoholic consumptions per week * Unstable body weight (weight gain or loss \>3 kg in the past three months) * Use of use of medication known to affect serum lipid metabolism * No severe medical conditions that might interfere with the study, such as high blood pressure, epilepsy, asthma, allergies, chronic obstructive pulmonary disease, inflammatory bowel diseases, auto inflammatory diseases and rheumatoid arthritis * Active cardiovascular disease like congestive heart failure or recent (\<6 months) event (acute myocardial infarction, cerebro vascular accident) * Use of an investigational product within the previous 1 month * Not willing to stop the consumption of foods rich in nitrates 3 weeks before the start of the study * Not willing to give up being a blood donor (or having donated blood) from 8 weeks before the start of the study, during the study or for 4 weeks after completion of the study * Not or difficult to venipuncture as evidenced during the screening visits

Design outcomes

Primary

MeasureTime frameDescription
Vascular activityChange from baseline at 2 hours after meal consumptionFlow-mediated dilation (FMD) of the brachial artery

Secondary

MeasureTime frameDescription
Arterial stiffnessChange from baseline at 3 hours after meal consumptionPulse wave analysis (PWA) and velocity (PWV)
Microcirculatory effectsChange from baseline at 3 hours after meal consumptionRetinal imaging
Metabolic risk markers related to the metabolic syndromeDuring 4 hours after meal consumptionChanges in biomarkers for low-grade systemic inflammation and endothelial activation.
Postprandial lipid metabolismDuring 4 hours after meal consumption
Postprandial glucose metabolismDuring 4 hours after meal consumption

Countries

Netherlands

Outcome results

None listed

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