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Changes in cholesterol kinetics following sugar cane policosanol supplementation: a randomized control trial

BACKGROUND: Sugar cane policosanols (SCP) have been shown to exert cholesterol-modulating properties in various studies conducted in Cuba by substantially reducing cholesterol synthesis. Independent research examining changes in cholesterol kinetics in response to SCP is limited to few studies, none...

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Autores principales: Kassis, Amira N, Jones, Peter JH
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2390548/
https://www.ncbi.nlm.nih.gov/pubmed/18447941
http://dx.doi.org/10.1186/1476-511X-7-17
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author Kassis, Amira N
Jones, Peter JH
author_facet Kassis, Amira N
Jones, Peter JH
author_sort Kassis, Amira N
collection PubMed
description BACKGROUND: Sugar cane policosanols (SCP) have been shown to exert cholesterol-modulating properties in various studies conducted in Cuba by substantially reducing cholesterol synthesis. Independent research examining changes in cholesterol kinetics in response to SCP is limited to few studies, none of which was able to replicate findings of the original research. Moreover, no data are available on the effect of SCP on cholesterol absorption to date. The present study was undertaken to determine effects on cholesterol kinetics, namely synthesis and absorption, within hypercholesterolemic individuals consuming a SCP treatment. Twenty-one otherwise healthy hypercholesterolemic subjects participated in a randomized double-blind crossover study where they received 10 mg/day of policosanols or a placebo incorporated in margarine as an evening snack for a period of 28 days. The last week of the study phase, subjects were given (13)C labelled cholesterol and deuterated water for the measurement of cholesterol absorption and synthesis respectively. Blood was collected on the first two and last five days of the trial. Cholesterol absorption and synthesis were determined by measuring red cell cholesterol (13)C and deuterium enrichment, respectively. RESULTS: There was no significant change in LDL cholesterol levels as compared to control. In addition, the area under the curve for red cell cholesterol (13)C enrichment across 96 hours was not significantly different in the SCP group as compared to control. Similarly, no difference was observed in the fractional rate of cholesterol synthesis over the period of 24 hours between the two treatment groups. CONCLUSION: The findings of the present study fail to support previous research concerning efficacy and mechanism of action for policosanols.
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spelling pubmed-23905482008-05-21 Changes in cholesterol kinetics following sugar cane policosanol supplementation: a randomized control trial Kassis, Amira N Jones, Peter JH Lipids Health Dis Research BACKGROUND: Sugar cane policosanols (SCP) have been shown to exert cholesterol-modulating properties in various studies conducted in Cuba by substantially reducing cholesterol synthesis. Independent research examining changes in cholesterol kinetics in response to SCP is limited to few studies, none of which was able to replicate findings of the original research. Moreover, no data are available on the effect of SCP on cholesterol absorption to date. The present study was undertaken to determine effects on cholesterol kinetics, namely synthesis and absorption, within hypercholesterolemic individuals consuming a SCP treatment. Twenty-one otherwise healthy hypercholesterolemic subjects participated in a randomized double-blind crossover study where they received 10 mg/day of policosanols or a placebo incorporated in margarine as an evening snack for a period of 28 days. The last week of the study phase, subjects were given (13)C labelled cholesterol and deuterated water for the measurement of cholesterol absorption and synthesis respectively. Blood was collected on the first two and last five days of the trial. Cholesterol absorption and synthesis were determined by measuring red cell cholesterol (13)C and deuterium enrichment, respectively. RESULTS: There was no significant change in LDL cholesterol levels as compared to control. In addition, the area under the curve for red cell cholesterol (13)C enrichment across 96 hours was not significantly different in the SCP group as compared to control. Similarly, no difference was observed in the fractional rate of cholesterol synthesis over the period of 24 hours between the two treatment groups. CONCLUSION: The findings of the present study fail to support previous research concerning efficacy and mechanism of action for policosanols. BioMed Central 2008-04-30 /pmc/articles/PMC2390548/ /pubmed/18447941 http://dx.doi.org/10.1186/1476-511X-7-17 Text en Copyright © 2008 Kassis and Jones; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Kassis, Amira N
Jones, Peter JH
Changes in cholesterol kinetics following sugar cane policosanol supplementation: a randomized control trial
title Changes in cholesterol kinetics following sugar cane policosanol supplementation: a randomized control trial
title_full Changes in cholesterol kinetics following sugar cane policosanol supplementation: a randomized control trial
title_fullStr Changes in cholesterol kinetics following sugar cane policosanol supplementation: a randomized control trial
title_full_unstemmed Changes in cholesterol kinetics following sugar cane policosanol supplementation: a randomized control trial
title_short Changes in cholesterol kinetics following sugar cane policosanol supplementation: a randomized control trial
title_sort changes in cholesterol kinetics following sugar cane policosanol supplementation: a randomized control trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2390548/
https://www.ncbi.nlm.nih.gov/pubmed/18447941
http://dx.doi.org/10.1186/1476-511X-7-17
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