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Body surface area-based omega-3 fatty acids supplementation strongly correlates to blood concentrations in children

•Omega-3-dose adjusted to BSA strongly correlated to blood omega-3 concentrations.•Results suggest a supplementation dose of 1500 mg/m2 BSA for further studies.•The DPA increase motivated an extended ω3-index, EDD index (∑EPA,DPA,DHA). Omega-3 fatty acids have been suggested as a complement in cance...

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Published in:Prostaglandins, leukotrienes and essential fatty acids leukotrienes and essential fatty acids, 2021-06, Vol.169, p.102285-102285, Article 102285
Main Authors: Ljungblad, L., Gleissman, H., Hedberg, G., Wickström, M., Eissler, N., Pickova, J., Johnsen, J.I., Tedroff, K., Strandvik, B., Kogner, P.
Format: Article
Language:English
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Summary:•Omega-3-dose adjusted to BSA strongly correlated to blood omega-3 concentrations.•Results suggest a supplementation dose of 1500 mg/m2 BSA for further studies.•The DPA increase motivated an extended ω3-index, EDD index (∑EPA,DPA,DHA). Omega-3 fatty acids have been suggested as a complement in cancer treatment, but doses are not established. We performed a dose-finding study in 33 children in remission from cancer. Participants were allocated to a body surface area (BSA) adjusted dose (mg/m2) of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) (40:60), ranging 233–3448 mg/m2 daily for 90 days. Fatty acid concentration in plasma phospholipids and red blood cells were determined by GC. Supplementation was well tolerated and correlated strongly with blood ω3-fatty acid concentrations and EPA showed the highest increase. Using the ω3-index disregards docosapentaenoic acid (DPA), which increased 30–43% in our study motivating an EDD-index (∑EPA,DPA,DHA). The ratio between arachidonic acid and EPA or DHA showed negative exponential trends. Dose per BSA enabled an individualized omega-3 supplementation decreasing the variation referred to interindividual differences. Based on our results, we suggest a dose of 1500 mg/m2 BSA for further studies.
ISSN:0952-3278
1532-2823
1532-2823
DOI:10.1016/j.plefa.2021.102285