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Published on: November 10, 2017
Effect of Plant Sterols on Cholesterol Oxidation Products in Statin-Treated Hypercholesterolemic Individuals: A Pilot
Diego Miedes1, Dario Mercatante2, Sonia Broseta1
1Nutrition and Food Science Area, Faculty of Pharmacy and Food Sciences, University of Valencia, Burjassot, Spain.
Insights
Plant sterols (PS) did not significantly reduce cholesterol oxidation products (COPs) in statin-treated individuals over six weeks. This study suggests PS supplementation may not be effective for lowering COPs in this population.
Area of Science:
- Cardiovascular Research
- Nutritional Science
- Pharmacology
Background:
- Cholesterol oxidation products (COPs) are implicated in cardiovascular diseases like atherosclerosis.
- Hypercholesterolemic individuals exhibit elevated COPs levels.
- Statins, while lowering cholesterol synthesis, do not prevent COP increase or endothelial damage.
Purpose of the Study:
- To investigate if plant sterols (PS) can reduce plasma COPs concentrations.
- To assess potential synergistic effects of PS with statin treatment.
- To evaluate the impact of PS supplementation on COPs in statin-treated hypercholesterolemic individuals.
Main Methods:
- A randomized, double-blind, parallel clinical trial (NCT05901246) involving 26 statin-treated hypercholesterolemic volunteers.
- Participants received either a PS food supplement (2 g/d) or a placebo for six weeks.
- Plasma COPs and cholesterol levels were analyzed using gas chromatography/mass spectrometry before and after intervention.
Main Results:
- No significant differences were observed in plasma cholesterol, total COPs, or individual COPs between the PS and placebo groups.
- COP levels did not correlate with physical or dietary habits.
- The six-week intervention with 2 g/d PS did not lead to a measurable reduction in COPs.
Conclusions:
- Plant sterol supplementation at 2 g/d for six weeks did not significantly reduce plasma COPs in statin-treated hypercholesterolemic individuals.
- The findings suggest a lack of measurable effect of PS on COPs in this specific cohort.
- Further research is needed to elucidate the interaction between statins, PS, and cholesterol oxidation for improved cardiovascular disease risk management strategies.
Abstract:
Cholesterol oxidation products (COPs) have been linked to inflammation, endothelial dysfunction, and atherosclerosis. COPs levels in hypercholesterolemic individuals are up to 50% higher than in healthy people. Although statins lower cholesterol synthesis, research demonstrates that they do not prevent an increase in COPs levels and the damage on endothelial cells. We hypothesized that plant sterols (PS) could reduce COPs concentrations, potentially offering a synergistic effect with statin treatment. This randomized, double-blind, parallel clinical trial investigates the effects of a PS-food supplement (2 g PS/d) on plasma COPs levels in statin-treated hypercholesterolemic individuals (ClinicalTrials.gov ID: NCT05901246). Twenty-six volunteers were randomly assigned to two groups and given either a PS supplement or a placebo for six weeks. Blood samples were taken before and after the treatment, and plasma was isolated. After sterol extraction and purification, COPs and cholesterol levels were analyzed by gas chromatography/mass spectrometry. There were no significant differences (p > 0.05) in plasma cholesterol (2276 ± 480 in control and 2169 ± 735 μg/mL in PS-treated subjects), total (1.12 ± 0.26 in control and 1.47 ± 0.48 μg/mL in PS-treated subjects) and single (α-epoxy-cholesterol, β-epoxy-cholesterol, cholestanetriol, 7α-hydroxy-cholesterol, 7β-hydroxy-cholesterol, and 7-keto-cholesterol) COPs levels between the two groups after the intervention; moreover, these levels were not associated with physical or dietary habits. These findings suggest that PS supplementation did not measurably reduce COPs concentrations over six weeks in this small sample of statin-treated individuals with relatively stable cholesterol levels. Future studies should explore the mechanisms underlying the interaction between statins, PS, and cholesterol oxidation to improve strategies for managing CVD risk.
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