Pycnogenol, French maritime pine bark extract, improves endothelial function of hypertensive patients.
- 2004-01
- Life sciences 74(7)
- Ximing Liu
- Junping Wei
- Fengsen Tan
- Shengming Zhou
- Gudrun Würthwein
- Peter Rohdewald
- PubMed: 14659974
- DOI: 10.1016/j.lfs.2003.07.037
Study Design
- Type
- Randomized Controlled Trial (RCT)
- Sample size
- n = 58
- Population
- 58 patients with hypertension
- Methods
- Placebo-controlled, double-blind, parallel group study; 100 mg Pycnogenol for 12 weeks
- Blinding
- Double-blind
- Duration
- 12 weeks
- Funding
- Unclear
Research Insights
concentrations of 6-keto prostaglandin F1a in plasma were significantly higher compared to placebo
- Effect
- Beneficial
- Effect size
- Small
- Dose
- 100 mg/day
Values for nitric oxide (NO) in plasma increased in both groups, but the differences were not significant
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg/day
Angiotensin II concentrations in plasma were lowered in the placebo group to a larger extent than in the Pycnogenol group.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg/day
Heart rate, electrolytes and blood urea nitrogen were not changed during treatment in both groups of patients.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg/day
Heart rate, electrolytes and blood urea nitrogen were not changed during treatment in both groups of patients.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg/day
The intake of Pycnogenol decreased endothelin-1 concentrations significantly compared to placebo
- Effect
- Beneficial
- Effect size
- Small
- Dose
- 100 mg/day
Heart rate, electrolytes and blood urea nitrogen were not changed during treatment in both groups of patients.
- Effect
- Neutral
- Effect size
- Small
- Dose
- 100 mg/day
Supplementation of the patients with 100 mg Pycnogenol over a period of 12 weeks helped to reduce the dose of the calcium antagonist nifedipine in a statistically significant manner.
- Effect
- Beneficial
- Effect size
- Small
- Dose
- 100 mg/day
Adverse Events Reported
Differences in rate of side effects were not statistically significant between the two groups.
- Finding
- No significant difference
- Significant
- No
Unwanted effects observed in both groups were of mild and transient nature, such as gastrointestinal problems, vertigo, headache and nausea.
- Finding
- Reported
- Grade
- mild
Unwanted effects observed in both groups were of mild and transient nature, such as gastrointestinal problems, vertigo, headache and nausea.
- Finding
- Reported
- Grade
- mild
Unwanted effects observed in both groups were of mild and transient nature, such as gastrointestinal problems, vertigo, headache and nausea.
- Finding
- Reported
- Grade
- mild
Unwanted effects observed in both groups were of mild and transient nature, such as gastrointestinal problems, vertigo, headache and nausea.
- Finding
- Reported
- Grade
- mild