Comparison of Pure Epicatechin and Cocoa on Markers of Vascular Function (FLAVO2)

Wageningen University

Status: Completed

Conditions: Endothelial Dysfunction; Bioavailability

Treatments: Dietary Supplement: Placebo; Dietary Supplement: Pure Epicatechin; Dietary Supplement: High flavan-3-ol cocoa

Study type: Interventional

Funder types: Other

Identifiers

NCT02221791

FLAVO2

Details and patient eligibility

About

Intervention studies support a protective effect of flavonoid-rich foods such as chocolate and tea on cardiovascular disease risk. In a previous study we found that pure epicatechin improves markers of vascular function and insulin resistance although the results were less pronounced than the majority of chocolate intervention studies.

The food matrix of chocolate or other compounds present in chocolate could play a role in the bioavailability of flavonoids, resulting in these heightened improvements in vascular function.

In this study we aim to compare the acute effects of pure epicatechin and high-flavonoid chocolate on markers of vascular function.

Full description

Twenty male participants between the ages of 40 and 80 will visit the university on three days, separated by a 2-week washout. During each visit the participants will, in random order, be allocated to one of the three interventions:

1. High flavan-3-ol chocolate (70g) plus placebo capsule;
2. White chocolate (70g) plus 100mg of epicatechin in capsule form;
3. White chocolate (70g) plus placebo capsule; Measurements of vascular function will be taken before, and 2 hours after consumption of the supplements. In order to determine flavonoid bioavailability, 24-hour urine samples will be collected and 7 blood samples will be taken over a period of 8 hours.

The primary study parameter is the percentage change in Flow-Mediated Dilation (FMD) as a result of a high-flavonoid cocoa or epicatechin challenge. Additional study parameters include plasma flavonoid and nitric oxide concentrations as well as pulse wave analysis parameters.

Enrollment: 20 patients

Sex: Male

Ages: 40 to 80 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Age between 40 and 80 years,
• BMI between > 20 and ≤ 30
• No reported current or previous metabolic diseases,
• No history of cardiovascular diseases,
• No history of renal, liver or thyroid diseases,
• No history of gastrointestinal diseases,
• No diagnosed diabetes mellitus,
• Fasting laboratory parameters within normal range as judged by the study physician: renal function (serum creatinine, ureum), liver function (ALAT, ASAT, GGT), serum glucose and HDL, LDL and total cholesterol.

Exclusion criteria

• Body mass index >30 or ≤20 kg/m2
• Usage of CVD medication (e.g. anti-hypertensive and/or lipid-modifying medication, non-steroidal anti-inflammatory drugs, acetylsalicylic acid), antibiotics, corticosteroids or opioids and not able or willing to stop taking them from at least 4 weeks prior to the study
• Taking nutritional supplements and unwilling to discontinue
• Reported dietary habits: medically prescribed diet, slimming diet
• Reported average alcohol consumption greater than or equal to 3 glasses/d
• Reported intense sporting activities > 10 h/w
• Weight loss or weight gain of 5 kg or more during the last 2 months
• Smokers
• Vegetarians
• Problems with consuming the supplements or following the study guidelines
• Recent blood donation (i.e. 1 month) prior to the study and/or planned donation during and shortly after the study period
• Not agreeing to be informed about unexpected and medically relevant personal test-results, or not agreeing that their general practitioner will be informed about these results
• Participation in another biomedical trial less than 2 months before the start of the study or at the same time
• No signed informed consent form
• Unable to comply with the study procedure (e.g. holidays, urine collection, blood sampling)

Trial design

Primary purpose: Basic Science

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Single Blind

---

20 participants in 3 patient groups, including a placebo group

Pure Epicatechin

Active Comparator group

Description:

Participants will consume 100mg of epicatechin (capsule) + 70g white chocolate

Treatment:

Dietary Supplement: Pure Epicatechin

High flavan-3-ol cocoa

Active Comparator group

Description:

Participants will consume 70g high flavan-3-ol cocoa (100mg epicatechin) + placebo capsule

Treatment:

Dietary Supplement: High flavan-3-ol cocoa

Placebo

Placebo Comparator group

Description:

Participants will consume 70g white chocolate + placebo capsules

Treatment:

Dietary Supplement: Placebo