Coconut Oil Supplementation Does Not Affect Blood Pressure Variability and Oxidative Stress: A Placebo-Controlled Clinical Study in Stage-1 Hypertensive Patients.
Francisco Antônio de Oliveira JuniorClara R RuizYohanna de OliveiraMarco A V BarrosAlexandre Sérgio SilvaMaria S B SantosVinícius J B MartinsCamille M BalariniValdir A BragaPublished in: Nutrients (2021)
Exploring an alternative to improve the clinical management of hypertension, we tested the hypothesis that food supplementation with coconut oil (EVCO), alone or combined with aerobic exercise training, could exert an antihypertensive effect (primary outcome) in patients with stage 1 hypertension. Forty-five hypertensive volunteers of both genders participated in a placebo-controlled clinical trial. The volunteers were submitted to 24-hour ambulatory blood pressure monitoring, analysis of blood pressure variability (BPV), measurement of serum malondialdehyde (MDA) and nutritional assessment. Results indicate that EVCO consumption had no adverse effects. The supplementation did not increase the caloric intake compared with placebo, and the dietary constituents were similar between groups, except for the saturated fats, especially lauric acid. The analysis of blood pressure indicated absence of antihypertensive effect of EVCO alone or combined with physical training. Furthermore, no effects on blood pressure variability and oxidative stress were observed in the supplemented hypertensive patients. Thus, despite the results observed in pre-clinical studies, the current clinical study did not provide evidence to support the use of coconut oil as an adjuvant in the management of hypertension in humans.
Keyphrases
- blood pressure
- hypertensive patients
- double blind
- placebo controlled
- oxidative stress
- heart rate
- clinical trial
- phase iii
- phase ii
- fatty acid
- study protocol
- dna damage
- blood glucose
- mental health
- early stage
- ischemia reperfusion injury
- skeletal muscle
- cell proliferation
- type diabetes
- insulin resistance
- signaling pathway
- diabetic rats
- radiation therapy
- high intensity
- metabolic syndrome
- risk assessment
- cell death
- locally advanced