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Omega-3 fatty acids and individual variability in plasma triglyceride response: A mini-review.
Rundblad, Amanda; Sandoval, Viviana; Holven, Kirsten B; Ordovás, José M; Ulven, Stine M.
Affiliation
  • Rundblad A; Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo, P.O Box 1046 Blindern, 0317, Oslo, Norway.
  • Sandoval V; Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo, P.O Box 1046 Blindern, 0317, Oslo, Norway; Escuela de Nutrición y Dietética, Facultad de Ciencias para el Cuidado de la Salud, Universidad San Sebastián, Gral. Lagos 1025, 5110693, Valdivia, Chile.
  • Holven KB; Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo, P.O Box 1046 Blindern, 0317, Oslo, Norway; Norwegian National Advisory Unit on Familial Hypercholesterolemia, Oslo University Hospital, Norway.
  • Ordovás JM; Nutrition and Genomics Laboratory, USDA ARS, JM-USDA Human Research Center on Aging at Tufts University, Boston, MA, USA; Nutritional Genomics and Epigenomics Group, Precision Nutrition and Obesity Program, IMDEA Food, CEI UAM + CSIC, Madrid, Spain; Centro de Investigación Biomédica en Red Fisiopato
  • Ulven SM; Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo, P.O Box 1046 Blindern, 0317, Oslo, Norway. Electronic address: smulven@medisin.uio.no.
Redox Biol ; 63: 102730, 2023 07.
Article in En | MEDLINE | ID: mdl-37150150
ABSTRACT
Cardiovascular disease (CVD) is a leading cause of death worldwide. Supplementation with the marine omega-3 fatty acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) is associated with lower CVD risk. However, results from randomized controlled trials that examine the effect of omega-3 supplementation on CVD risk are inconsistent. This risk-reducing effect may be mediated by reducing inflammation, oxidative stress and serum triglyceride (TG) levels. However, not all individuals respond by reducing TG levels after omega-3 supplementation. This inter-individual variability in TG response to omega-3 supplementation is not fully understood. Hence, we aim to review the evidence for how interactions between omega-3 fatty acid supplementation and genetic variants, epigenetic and gene expression profiling, gut microbiota and habitual intake of omega-3 fatty acids can explain why the TG response differs between individuals. This may contribute to understanding the current controversies and play a role in defining future personalized guidelines to prevent CVD.
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Full text: 1 Database: MEDLINE Main subject: Cardiovascular Diseases / Fatty Acids, Omega-3 Type of study: Clinical_trials Language: En Journal: Redox Biol Year: 2023 Type: Article Affiliation country: Norway

Full text: 1 Database: MEDLINE Main subject: Cardiovascular Diseases / Fatty Acids, Omega-3 Type of study: Clinical_trials Language: En Journal: Redox Biol Year: 2023 Type: Article Affiliation country: Norway