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Impact of Oranges on Cardiovascular Health

Bioavailability of Flavanones Compounds and Their Impact on Cardiovascular Health

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01935362
Enrollment
25
Registered
2013-09-05
Start date
2013-06-30
Completion date
2014-03-31
Last updated
2014-04-01

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

Conditions

Blood Pressure, Cardiovascular Disease Risk Reduction, Endothelial Dysfunction

Keywords

Flavanones, Bioavailability, Blood vessel health, Blood glucose

Brief summary

Cardiovascular disease (CVD) is the leading cause of deaths in the Western world. Established risk factors include high LDL cholesterol, high blood pressure and diabetes. Poor blood vessel health is considered a predictor of future CVD risk, but can be reversed. Several different measurements can be used to determine blood vessel health; such as blood pressure (BP), and newer techniques which measure blood flow through the arteries after a blood pressure cuff restricts blood flow for a few minutes in one arm. Flavonoids are compounds found in plant-based foods, and are associated with a reduced risk of CVD. From the previous studies, there is strong evidence that orange juice and citrus foods which have higher amount of specific citrus flavonoids improved cardiovascular risk factors such as BP and blood vessel health. Absorption of citrus flavonoids occurs in the colon after bacteria breakdown the forms found in food. After the flavonoids are absorbed into the blood they are modification by liver enzymes before they are excreted in the urine. A large range of citrus flavonoid have been found excreted in the urinary, ranging anywhere from 0-57% of the dose. Variation in the potential health effect may reflect the level of the citrus flavonoid absorbed, and this is not often considered in human studies. This study is a 4-week double-blinded, randomized, cross-over intervention trial using a commercially-available orange juice supplement and a placebo control. The aims of the study are to determine whether orange juice supplements reduce blood pressure and improve blood vessel health after 4 weeks. Furthermore, to determine if there is a relationship between absorption of flavonoids (as measured by urinary excretion) and changes in blood pressure or blood vessel health. The participants will need to attend 4 sessions on 4 separate study days, every 4 weeks for 12 weeks. On each study day they will have their weight, height, waist circumference, and blood pressure measured. A finger-prick blood sample, using a single-use lancet (Accu-Chek Safe T Pro Plus), will be taken to check the fasting blood glucose level. Blood flow in fingertips will be monitored before and after reducing blood flow in your forearm using a blood pressure cuff (called an EndoPAT). Participants will be asked to collect urine for 24 hr on each of the study days, and to consume the supplements provided daily for two sets of 4 weeks (there will be 4 weeks in the middle without any supplements). An improvement in blood pressure and/or blood flow will provide evidence that blood vessel health has improved through short-term (4 week) use of a citrus flavonoid supplement

Interventions

DIETARY_SUPPLEMENTCitrus supplement
DIETARY_SUPPLEMENTPlacebo

Sponsors

Dr Andrea Day and Prof Gary Williamson
CollaboratorUNKNOWN
University of Leeds
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* No known cardiovascular disease or diabetes * Age between 30-60 years * Heavier than average (Body mass index, BMI ≥ 25 kg/m2) * Currently non smoker * Willing to consume orange juice supplements for 2 months * Male and female are equally eligible as not mentioned on advert

Exclusion criteria

* Those who Taken any antibiotics in the 2 months prior to the study * Those who consume dietary or herbal supplements * previous surgery on gastrointestinal tract * Those who currently taking medication * Current smokers, or ex-smokers ceasing \< 3 months ago * pregnant or breast feeding * Those with known allergies to the intervention treatment

Design outcomes

Primary

MeasureTime frameDescription
blood pressureBaseline and 4 weeksChange in systolic and diastolic blood pressure
An improvement in blood flowBaseline and 4 weeksChange in blood flow using Endo-PAT device

Secondary

MeasureTime frameDescription
blood glucoseBaseline and 4 weeksChange in blood glucose level in plasma,
bioavailability of flavanones compoundsBaseline and 4 weeksChange of urine flavanones from the baseline and after 4 weeks of each arm

Countries

United Kingdom

Outcome results

None listed

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