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Evidence-Based Supplement Research
Evidence-Based Supplement Research

Short-term cocoa bioflavanol supplementation does not improve cold-induced vasodilation in young healthy adults.

  • 2023-12-27
  • European journal of applied physiology 124(5)
    • Billie K Alba
    • Andrew M Greenfield
    • Beau R Yurkevicius
    • Myra L Jones
    • John W Castellani

Study Design

Type
Randomized Controlled Trial (RCT)
Population
Eleven healthy adults (24 ± 6 years; 10 M/1F)
Methods
Double-blind, randomized, crossover design; 8 days of 900 mg/day cocoa flavanols or matched placebo; CIVD assessed on Days 1 and 8 with finger immersion protocol
Blinding
Double-blind
Duration
8 days
Funding
Unclear

Purpose

Cold-induced vasodilation (CIVD) is an oscillatory rise in blood flow to glabrous skin that occurs in cold-exposed extremities. Dietary flavanols increase bioavailable nitric oxide, a proposed mediator of CIVD through active vasodilation and/or withdrawal of sympathetic vascular smooth muscle tone. However, no studies have examined the effects of flavanol intake on extremity skin perfusion during cold exposure. We tested the hypothesis that acute and 8-day flavanol supplementation would augment CIVD during single-digit cold water immersion (CWI).

Methods

Eleven healthy adults (24 ± 6 years; 10 M/1F) ingested cocoa flavanols (900 mg/day) or caffeine- and theobromine-matched placebo for 8 days in a double-blind, randomized, crossover design. On Days 1 and 8, CIVD was assessed 2 h post-treatment. Subjects immersed their 3rd finger in warm water (42 °C) for 15 min before CWI (4 °C) for 30 min, during which nail bed and finger pad skin temperature were measured.

Results

Flavanol ingestion had no effect on CIVD frequency (Day 1, Flavanol: 3 ± 2 vs. Placebo: 3 ± 2; Day 8, Flavanol: 3 ± 2 vs. Placebo: 3 ± 1) or amplitude (Day 1, Flavanol: 4.3 ± 1.7 vs. Placebo: 4.9 ± 2.6 °C; Day 8, Flavanol: 3.9 ± 1.9 vs. Placebo: 3.9 ± 2.0 °C) in the finger pad following acute or 8-day supplementation (P > 0.05). Furthermore, average, nadir, and apex finger pad temperatures during CWI were not different between treatments on Days 1 or 8 of supplementation (P > 0.05). Similarly, no differences in CIVD parameters were observed in the nail bed following supplementation (P > 0.05).

Conclusion

These data suggest that cocoa flavanol ingestion does not alter finger CIVD. Clinical Trial Registration Clinicaltrials.gov Identifier: NCT04359082. April 24, 2020.

Research Insights

  • Similarly, no differences in CIVD parameters were observed in the nail bed following supplementation (P > 0.05).

    Effect
    Neutral
    Effect size
    Small
    Dose
    900 mg/day
  • Flavanol ingestion had no effect on ... amplitude (Day 1, Flavanol: 4.3 ± 1.7 vs. Placebo: 4.9 ± 2.6 °C; Day 8, Flavanol: 3.9 ± 1.9 vs. Placebo: 3.9 ± 2.0 °C) in the finger pad following acute or 8-day supplementation (P > 0.05).

    Effect
    Neutral
    Effect size
    Small
    Dose
    900 mg/day
  • Flavanol ingestion had no effect on CIVD frequency (Day 1, Flavanol: 3 ± 2 vs. Placebo: 3 ± 2; Day 8, Flavanol: 3 ± 2 vs. Placebo: 3 ± 1) ... in the finger pad following acute or 8-day supplementation (P > 0.05).

    Effect
    Neutral
    Effect size
    Small
    Dose
    900 mg/day
  • average, nadir, and apex finger pad temperatures during CWI were not different between treatments on Days 1 or 8 of supplementation (P > 0.05)

    Effect
    Neutral
    Effect size
    Small
    Dose
    900 mg/day
  • average, nadir, and apex finger pad temperatures during CWI were not different between treatments on Days 1 or 8 of supplementation (P > 0.05)

    Effect
    Neutral
    Effect size
    Small
    Dose
    900 mg/day
  • Furthermore, average, nadir, and apex finger pad temperatures during CWI were not different between treatments on Days 1 or 8 of supplementation (P > 0.05).

    Effect
    Neutral
    Effect size
    Small
    Dose
    900 mg/day
  • Furthermore, average, nadir, and apex finger pad temperatures during CWI were not different between treatments on Days 1 or 8 of supplementation (P > 0.05).

    Effect
    Neutral
    Effect size
    Small
    Dose
    900 mg/day
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