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RBC and WBC fatty acid composition following consumption of an omega 3 supplement: Lessons for future clinical trials

BACKGROUND: Results from increasing numbers of in vitro and in vivo studies have demonstrated that omega 3 fatty acids incorporated in cell culture media or in the diet of the animals can suppress the growth of cancers. When human clinical trials are initiated to determine the ability of omega 3 fat...

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Autores principales: Witte, Theodore R, Salazar, Alexander J, Ballester, Oscar F, Hardman, W Elaine
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846941/
https://www.ncbi.nlm.nih.gov/pubmed/20307284
http://dx.doi.org/10.1186/1476-511X-9-31
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author Witte, Theodore R
Salazar, Alexander J
Ballester, Oscar F
Hardman, W Elaine
author_facet Witte, Theodore R
Salazar, Alexander J
Ballester, Oscar F
Hardman, W Elaine
author_sort Witte, Theodore R
collection PubMed
description BACKGROUND: Results from increasing numbers of in vitro and in vivo studies have demonstrated that omega 3 fatty acids incorporated in cell culture media or in the diet of the animals can suppress the growth of cancers. When human clinical trials are initiated to determine the ability of omega 3 fatty acids to alter growth or response to chemotherapeutic interventions of cancers, it will be essential to determine the omega 3 intake of individuals in the trial to determine compliance with consumption of the supplement and to correlate with endpoints of efficacy. We wondered if the fatty acid composition of RBCs might accurately indicate incorporation of omega 3 fatty acids in the WBCs. In this report we determine and compare the changes in fatty acid compositions of red blood cells and white blood cells in response to consumption of three doses of an omega 3 fatty acid supplement. RESULTS: We found that the fraction of omega 3 fatty acids in both red blood cells and white blood cells increased following consumption of the supplement. There was a linear, dose responsive increase in the fraction of omega 3 fatty acids in red blood cells but the increase in omega 3 in white blood cells was not linear. The magnitude of increase in omega 3 fatty acids was different between the two cell types. CONCLUSIONS: Fatty acid analysis of red blood cells is a good measure of compliance with supplement consumption. However, fatty acid analysis of white blood cells is needed to correlate changes in fatty acid composition of white blood cells with other biochemical changes in the white blood cells. TRIAL REGISTRATION: ClinicalTrials.gov NCT00899353.
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spelling pubmed-28469412010-03-30 RBC and WBC fatty acid composition following consumption of an omega 3 supplement: Lessons for future clinical trials Witte, Theodore R Salazar, Alexander J Ballester, Oscar F Hardman, W Elaine Lipids Health Dis Research BACKGROUND: Results from increasing numbers of in vitro and in vivo studies have demonstrated that omega 3 fatty acids incorporated in cell culture media or in the diet of the animals can suppress the growth of cancers. When human clinical trials are initiated to determine the ability of omega 3 fatty acids to alter growth or response to chemotherapeutic interventions of cancers, it will be essential to determine the omega 3 intake of individuals in the trial to determine compliance with consumption of the supplement and to correlate with endpoints of efficacy. We wondered if the fatty acid composition of RBCs might accurately indicate incorporation of omega 3 fatty acids in the WBCs. In this report we determine and compare the changes in fatty acid compositions of red blood cells and white blood cells in response to consumption of three doses of an omega 3 fatty acid supplement. RESULTS: We found that the fraction of omega 3 fatty acids in both red blood cells and white blood cells increased following consumption of the supplement. There was a linear, dose responsive increase in the fraction of omega 3 fatty acids in red blood cells but the increase in omega 3 in white blood cells was not linear. The magnitude of increase in omega 3 fatty acids was different between the two cell types. CONCLUSIONS: Fatty acid analysis of red blood cells is a good measure of compliance with supplement consumption. However, fatty acid analysis of white blood cells is needed to correlate changes in fatty acid composition of white blood cells with other biochemical changes in the white blood cells. TRIAL REGISTRATION: ClinicalTrials.gov NCT00899353. BioMed Central 2010-03-22 /pmc/articles/PMC2846941/ /pubmed/20307284 http://dx.doi.org/10.1186/1476-511X-9-31 Text en Copyright ©2010 Witte et al; 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
Witte, Theodore R
Salazar, Alexander J
Ballester, Oscar F
Hardman, W Elaine
RBC and WBC fatty acid composition following consumption of an omega 3 supplement: Lessons for future clinical trials
title RBC and WBC fatty acid composition following consumption of an omega 3 supplement: Lessons for future clinical trials
title_full RBC and WBC fatty acid composition following consumption of an omega 3 supplement: Lessons for future clinical trials
title_fullStr RBC and WBC fatty acid composition following consumption of an omega 3 supplement: Lessons for future clinical trials
title_full_unstemmed RBC and WBC fatty acid composition following consumption of an omega 3 supplement: Lessons for future clinical trials
title_short RBC and WBC fatty acid composition following consumption of an omega 3 supplement: Lessons for future clinical trials
title_sort rbc and wbc fatty acid composition following consumption of an omega 3 supplement: lessons for future clinical trials
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2846941/
https://www.ncbi.nlm.nih.gov/pubmed/20307284
http://dx.doi.org/10.1186/1476-511X-9-31
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