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Predicting the effects of supplemental EPA and DHA on the omega-3 index.
Walker, Rachel E; Jackson, Kristina Harris; Tintle, Nathan L; Shearer, Gregory C; Bernasconi, Aldo; Masson, Serge; Latini, Roberto; Heydari, Bobak; Kwong, Raymond Y; Flock, Michael; Kris-Etherton, Penny M; Hedengran, Anne; Carney, Robert M; Skulas-Ray, Ann; Gidding, Samuel S; Dewell, Antonella; Gardner, Christopher D; Grenon, S Marlene; Sarter, Barbara; Newman, John W; Pedersen, Theresa L; Larson, Mark K; Harris, William S.
Afiliación
  • Walker RE; Department of Nutritional Sciences, The Pennsylvania State University, University Park, PA, USA.
  • Jackson KH; OmegaQuant Analytics, LLC, Sioux Falls, SD, USA.
  • Tintle NL; Department of Mathematics and Statistics, Dordt College, Sioux Center, IA, USA.
  • Shearer GC; Department of Nutritional Sciences, The Pennsylvania State University, University Park, PA, USA.
  • Bernasconi A; Department of Internal Medicine, Sanford School of Medicine, University of South Dakota, Sioux Falls, SD, USA.
  • Masson S; Global Organization for EPA and DHA, Salt Lake City, UT, USA.
  • Latini R; Department of Cardiovascular Research, Institute of Pharmacological Research "Mario Negri," Milan, Italy.
  • Heydari B; Department of Cardiovascular Research, Institute of Pharmacological Research "Mario Negri," Milan, Italy.
  • Kwong RY; Libin Cardiovascular Institute of Alberta, University of Calgary, Calgary, Alberta, Canada.
  • Flock M; Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Kris-Etherton PM; Clinical and Translational Science Institute, University of Pittsburgh, Pittsburgh, PA, USA.
  • Hedengran A; Department of Nutritional Sciences, The Pennsylvania State University, University Park, PA, USA.
  • Carney RM; Department of Ophthalmology, Rigshospitalet, Glostrup, Denmark.
  • Skulas-Ray A; Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA.
  • Gidding SS; Department of Nutritional Sciences, University of Arizona, Tucson, AZ, USA.
  • Dewell A; Familial Hypercholesterolemia Foundation, Pasadena, CA, USA.
  • Gardner CD; Stanford Prevention Research Center, Stanford University, Stanford, CA, USA.
  • Grenon SM; Stanford Prevention Research Center, Stanford University, Stanford, CA, USA.
  • Sarter B; Department of Surgery, University of California, San Francisco, San Francisco, CA, USA.
  • Newman JW; Department of Naturopathic Medicine, Bastyr University, San Diego, CA, USA.
  • Pedersen TL; Obesity and Metabolism Research Unit, Western Human Nutrition Research Center, Agricultural Research Service, US Department of Agriculture, Davis, CA, USA.
  • Larson MK; Department of Food Science and Technology, University of California, Davis, Davis, CA, USA.
  • Harris WS; Department of Biology, Augustana University, Sioux Falls, SD, USA.
Am J Clin Nutr ; 110(4): 1034-1040, 2019 10 01.
Article en En | MEDLINE | ID: mdl-31396625
BACKGROUND: Supplemental long-chain omega-3 (n-3) fatty acids (EPA and DHA) raise erythrocyte EPA + DHA [omega-3 index (O3I)] concentrations, but the magnitude or variability of this effect is unclear. OBJECTIVE: The purpose of this study was to model the effects of supplemental EPA + DHA on the O3I. METHODS: Deidentified data from 1422 individuals from 14 published n-3 intervention trials were included. Variables considered included dose, baseline O3I, sex, age, weight, height, chemical form [ethyl ester (EE) compared with triglyceride (TG)], and duration of treatment. The O3I was measured by the same method in all included studies. Variables were selected by stepwise regression using the Bayesian information criterion. RESULTS: Individuals supplemented with EPA + DHA (n = 846) took a mean ± SD of 1983 ± 1297 mg/d, and the placebo controls (n = 576) took none. The mean duration of supplementation was 13.6 ± 6.0 wk. The O3I increased from 4.9% ± 1.7% to 8.1% ± 2.7% in the supplemented individuals ( P < 0.0001). The final model included dose, baseline O3I, and chemical formulation type (EE or TG), and these explained 62% of the variance in response (P < 0.0001). The model predicted that the final O3I (and 95% CI) for a population like this, with a baseline concentration of 4.9%, given 850 mg/d of EPA + DHA EE would be ∼6.5% (95% CI: 6.3%, 6.7%). Gram for gram, TG-based supplements increased the O3I by about 1 percentage point more than EE products. CONCLUSIONS: Of the factors tested, only baseline O3I, dose, and chemical formulation were significant predictors of O3I response to supplementation. The model developed here can be used by researchers to help estimate the O3I response to a given EPA + DHA dose and chemical form.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ácido Eicosapentaenoico / Ácidos Docosahexaenoicos / Eritrocitos / Modelos Biológicos Tipo de estudio: Clinical_trials / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Am J Clin Nutr Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ácido Eicosapentaenoico / Ácidos Docosahexaenoicos / Eritrocitos / Modelos Biológicos Tipo de estudio: Clinical_trials / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Am J Clin Nutr Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos
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