Two trials separately measured the bioavailability and impact on inflammation of a supplement taken daily containing 510 mg Docosahexaenoic acid (DHA), 344 mg Eicosapentaenoic acid (EPA), and 1000 IU of vitamin D (25-hydroxyvitamin D; 25(OH)D), for healthy and Crohn's disease (CD) populations. Both trials were double blinded, randomized, placebo-controlled with cross-over. Participants were randomly allocated to groups A (placebo then supplement) or B (supplement then placebo). Both included a washout. Fatty acid (-3 PUFAs) and vitamin D serum levels, plasma C-reactive protein (CRP), and stool calprotectin were measured before and after each treatment period. Outcome measures were analyzed using generalized linear mixed models, including terms for treatment, period, and a treatment-by-period interaction. The supplement significantly increased serum levels in healthy and CD groups for EPA ( < 0.001 and < 0.001, respectively), Docosapentaenoic acid ( < 0.001 and 0.005), DHA ( < 0.001 and 0.006), the omega-3 index ( < 0.001 and 0.001), and (vitamin D ( < 0.001 and 0.027). CRP and calprotectin measures showed no evidence of a treatment effect on inflammation; however, model estimation was imprecise for both outcomes, hence further research is required to elucidate potential inflammation effects. The nutrient supplement increased serum levels of key -3 PUFAs and vitamin D in both populations, showing the preparation was readily bioavailable.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7230517PMC
http://dx.doi.org/10.3390/nu12041139DOI Listing

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