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  • Role of Polyunsaturated Fat...
    Laguzzi, Federica; Åkesson, Agneta; Marklund, Matti; Qian, Frank; Gigante, Bruna; Bartz, Traci M; Bassett, Julie K; Birukov, Anna; Campos, Hannia; Hirakawa, Yoichiro; Imamura, Fumiaki; Jäger, Susanne; Lankinen, Maria; Murphy, Rachel A; Senn, Mackenzie; Tanaka, Toshiko; Tintle, Nathan; Virtanen, Jyrki K; Yamagishi, Kazumasa; Allison, Matthew; Brouwer, Ingeborg A; De Faire, Ulf; Eiriksdottir, Gudny; Ferrucci, Luigi; Forouhi, Nita G; Geleijnse, Johanna M; Hodge, Allison M; Kimura, Hitomi; Laakso, Markku; Risérus, Ulf; van Westing, Anniek C; Bandinelli, Stefania; Baylin, Ana; Giles, Graham G; Gudnason, Vilmundur; Iso, Hiroyasu; Lemaitre, Rozenn N; Ninomiya, Toshiharu; Post, Wendy S; Psaty, Bruce M; Salonen, Jukka T; Schulze, Matthias B; Tsai, Michael Y; Uusitupa, Matti; Wareham, Nicholas J; Oh, Seung-Won; Wood, Alexis C; Harris, William S; Siscovick, David; Mozaffarian, Dariush; Leander, Karin

    Circulation (New York, N.Y.), 01/2024, Letnik: 149, Številka: 4
    Journal Article

    It is unknown whether dietary intake of polyunsaturated fatty acids (PUFA) modifies the cardiovascular disease (CVD) risk associated with a family history of CVD. We assessed interactions between biomarkers of low PUFA intake and a family history in relation to long-term CVD risk in a large consortium. Blood and tissue PUFA data from 40 885 CVD-free adults were assessed. PUFA levels ≤25th percentile were considered to reflect low intake of linoleic, alpha-linolenic, and eicosapentaenoic/docosahexaenoic acids (EPA/DHA). Family history was defined as having ≥1 first-degree relative who experienced a CVD event. Relative risks with 95% CI of CVD were estimated using Cox regression and meta-analyzed. Interactions were assessed by analyzing product terms and calculating relative excess risk due to interaction. After multivariable adjustments, a significant interaction between low EPA/DHA and family history was observed (product term pooled RR, 1.09 95% CI, 1.02-1.16; =0.01). The pooled relative risk of CVD associated with the combined exposure to low EPA/DHA, and family history was 1.41 (95% CI, 1.30-1.54), whereas it was 1.25 (95% CI, 1.16-1.33) for family history alone and 1.06 (95% CI, 0.98-1.14) for EPA/DHA alone, compared with those with neither exposure. The relative excess risk due to interaction results indicated no interactions. A significant interaction between biomarkers of low EPA/DHA intake, but not the other PUFA, and a family history was observed. This novel finding might suggest a need to emphasize the benefit of consuming oily fish for individuals with a family history of CVD.