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Anthocyanin-rich Blackcurrant and Vascular Function

Effects of an Anthocyanin-rich Blackcurrant Beverage on Cardiovascular Function

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02459756
Enrollment
23
Registered
2015-06-02
Start date
2015-06-30
Completion date
2015-11-30
Last updated
2016-02-09

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

Conditions

Inflammation, Vascular Stiffness

Keywords

anthocyanins, bioavailability

Brief summary

Regular consumption of fruits and vegetables may improve human health and reduce the risk of chronic diseases, such as heart disease, certain cancers and type 2 diabetes, but the active components and the underlying mechanisms are poorly understood. Berry fruits are abundant in anthocyanins and this study aims to test the hypothesis that ingestion of an anthocyanin-rich blackcurrant beverage will improve markers of cardiovascular health (health of blood vessels, inflammation and platelet function). Further, the study will investigate the anthocyanin bioavailability from the blackcurrant beverage.

Interventions

OTHERBeverage: Spray dried blackcurrant powder dissolved in water
OTHERBeverage: Placebo (sucrose, glucose, fructose, maltodextrin, malic acid, citric acid, vitamin C, artificial blackcurrant flavouring and low-nitrate water)

Sponsors

GlaxoSmithKline
CollaboratorINDUSTRY
University of Reading
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
30 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 30-55 years * Non-smoker * BMI between 20 - 30 kg/m2 * Generally healthy as established by a 'health and lifestyle' questionnaire and a screening blood sample * Blood pressure \< 140/90mmHg * Total cholesterol \< 6.2 mmol/L * Fasting glucose \< 7.0 mmol/L

Exclusion criteria

* Diabetes mellitus * Heart problems, stroke, vascular disease * Inflammatory disease * Kidney, liver, pancreas or gastrointestinal diseases * Medication for hyperlipidaemia, hypertension, hypercoagulation, inflammatory conditions * Asthma * Allergies * Smokers (social smokers who agree to abstain for 1 month before and during the study not excluded) * Taking phytochemical, antioxidant or fish oil supplements (unless willing to stop for the study period) * Taking aspirin \> 2 times per month and unwilling to abstain from aspirin ingestion for 14 days prior each study visit * History of alcohol misuse * Consumption of alcohol \>21 units (men) or \>15 units (women) * Vegans * Intense aerobic exercise \>20 min 3 x per week * Participation in another clinical trial * Antibiotics in previous 3 months before study * Low haemoglobin levels * Females who are pregnant, lactating, or if of reproductive age and not using a reliable form of contraception (including abstinence)

Design outcomes

Primary

MeasureTime frame
Change from baseline in vascular reactivity measured by flow-mediated dilatation (FMD)Acute study: measured at baseline and 1, 2, 4 and 6 h post intervention
Change from baseline in platelet function measured by agonist-induced platelet aggregationAcute study: measured at baseline and 2 and 4 h post intervention

Secondary

MeasureTime frame
Change from baseline in blood pressureAcute study: measured at baseline and 1, 2, 4 and 6 h post intervention
Change from baseline in the concentration of nitric oxide in plasma measured by ozone-based chemiluminescenceAcute study: measured at baseline and 1, 2, 4 and 6 h post intervention
Change from baseline in the concentration of polyphenols and their metabolites and degradants in blood and urine samples measured by HPLC-MS/MSAcute study: plasma measured at baseline and 1, 2, 4, 6 and 24 h post intervention, urine measured at baseline and 1, 2, 4, 6 and 6-24 h post intervention
Change from baseline in platelet function (numbers of circulating micro particles by nano particle tracking analysis)Acute study: measured at baseline and 1, 2, 4 and 6 h post intervention (urine metabonomics additionally 6-24h)
Metabonomics on urine and plasma samples measured by nuclear magnetic resonance spectroscopyAcute study: measured at baseline and 1, 2, 4 and 6 h post intervention (urine metabonomics additionally 6-24h)
Change from baseline in the concentration of selected cytokines (TNF-a, IL-1b, IL-6, IL-8 and IL-10) in plasma measured using a cytometric bead array kit from BD BiosciencesAcute study: measured at baseline and 1, 2, 4 and 6 h post intervention
Change from baseline in vascular function measured by digital volume pulse (DVP)Acute study: measured at baseline and 2, 4 and 6 h post intervention

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026