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Investigating the Acute Effects of Flavonoids in Blueberries on Cognitive Function.

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University of Reading

Status

Completed

Conditions

Healthy Adults.

Treatments

Dietary Supplement: Flavonoids
Dietary Supplement: Control

Study type

Interventional

Funder types

Other

Identifiers

NCT01289860
UReading_2010_01

Details and patient eligibility

About

This study was a controlled, cross-over, acute flavonoid intervention trial with younger and older adults. Subjects consumed a blueberry beverage during one visit and a control beverage on another. Cognitive function pre drink was assessed, blood and urine samples were taken as well as blood pressure and a measure of vascular reactivity. These outcome measures were taken at 2 and 5 hours post drink.

It was predicted that the flavonoids in the blueberry drink would lead to improved performance on the cognitive tests and vascular reactivity measure compared to following the control drink. It was thought this could be due to increased vaso-dilation and improving blood flow to the brain which was investigated in an extension to the project where a sample of individuals underwent brain imaging in an MRI scanner pre and post a blueberry and a control drink.

Full description

The control drink was matched to the blueberry drink for other bioactive compounds which may have affected cognition, specifically sugars and vitamin C. Volunteers were healthy, not on any medication, without high blood pressure, high cholesterol, high BMI, diabetes or other medical conditions. Older adults were aged 61-75 years and younger adults 18-26 years.

Blood and urine samples will be analysed for flavonoid levels and Brain Derived Neurotrophic Factor, a biomarker of memory and learning, flavonoids may lead to increased BDNF production through the ERK-CREB-BDNF pathway.

Flavonoids may also increase nitric oxide production and improve the flexibility of the blood vessels hence the measure of vascular reactivity using the Digital Volume Pulse machine. This can lead to increased vaso-dilation and blood flow to the brain, therefore an fMRI study was carried out the investigate this using arterial spin labeling following acute blueberry supplementation compared to a control drink.

Enrollment

47 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • No medical conditions
  • Not taking any medication or supplements (or willing to stop taking supplements for duration of study)
  • Not lactose intolerant
  • Willing to give blood and urine samples
  • Not partaking in frequent vigorous exercise
  • Not suffering from or history of depression

Exclusion criteria

  • On blood pressure medication, taking Aspirin or other blood thinning medication
  • BMI > 30
  • Cholesterol > 6
  • Diabetes or other serious medical condition
  • Lactose intolerant
  • Any learning difficulty e.g. dyslexia

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

47 participants in 2 patient groups, including a placebo group

Blueberry drink
Active Comparator group
Description:
30g of blueberry powder (equivalent to 200g fresh blueberries) and 300ml of semi-skimmed milk
Treatment:
Dietary Supplement: Flavonoids
Control drink
Placebo Comparator group
Description:
29g of powder consisting of sugars and vitamin C, values of which were matched to that of the blueberry drink, with 1 g of citric acid to match for taste.
Treatment:
Dietary Supplement: Control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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