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Journal of Lipid Research
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    • Patient-Oriented and Epidemiological Research
      Open Access

      DHA intake interacts with ELOVL2 and ELOVL5 genetic variants to influence polyunsaturated fatty acids in human milk

      Journal of Lipid Research
      Vol. 60Issue 5p1043–1049Published online: March 26, 2019
      • Yixia Wu霞吴义
      • Yan Wang 烟王
      • Huimin Tian敏田慧
      • Tong Lu逯通
      • Miao Yu苗于
      • Wenhui Xu慧徐文
      • and others
      Cited in Scopus: 16
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        Endogenous synthesis of PUFAs is mediated by genes controlling fatty acid elongases 2 and 5 (ELOVL2 and ELOVL5) and by exogenous DHA intake. Associations between elongases and PUFA levels probably involve genetic variants of ELOVL and changes in DHA intake, but data about their combined effect on PUFA levels are sparse. We hypothesized that each factor would directly affect PUFAs and that interactions between haplotypes and DHA intake would influence PUFAs. We explored four levels of DHA intake in pregnant Chinese Han women and 10 SNPs in the ELOVL genes to determine associations with PUFAs in breast milk.
        DHA intake interacts with ELOVL2 and ELOVL5 genetic variants to influence polyunsaturated fatty acids in human milk
      • Patient-Oriented and Epidemiological Research
        Open Access

        Differential effects of EPA versus DHA on postprandial vascular function and the plasma oxylipin profile in men

        Journal of Lipid Research
        Vol. 57Issue 9p1720–1727Published online: May 11, 2016
        • Seán McManus
        • Noemi Tejera
        • Khader Awwad
        • David Vauzour
        • Neil Rigby
        • Ingrid Fleming
        • and others
        Cited in Scopus: 25
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          Our objective was to investigate the impact of EPA versus DHA on arterial stiffness and reactivity and underlying mechanisms (with a focus on plasma oxylipins) in the postprandial state. In a three-arm crossover acute test meal trial, men (n = 26, 35–55 years) at increased CVD risk received a high-fat (42.4 g) test meal providing 4.16 g of EPA or DHA or control oil in random order. At 0 h and 4 h, blood samples were collected to quantify plasma fatty acids, long chain n-3 PUFA-derived oxylipins, nitrite and hydrogen sulfide, and serum lipids and glucose.
          Differential effects of EPA versus DHA on postprandial vascular function and the plasma oxylipin profile in men
        • Patient-Oriented and Epidemiological Research
          Open Access

          Effects of n-3 FA supplementation on the release of proresolving lipid mediators by blood mononuclear cells: the OmegAD study

          Journal of Lipid Research
          Vol. 56Issue 3p674–681Published online: January 23, 2015
          • Xiuzhe Wang
          • Erik Hjorth
          • Inger Vedin
          • Maria Eriksdotter
          • Yvonne Freund-Levi
          • Lars-Olof Wahlund
          • and others
          Cited in Scopus: 59
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            Specialized proresolving mediators (SPMs) induce resolution of inflammation. SPMs are derivatives of n-3 and n-6 PUFAs and may mediate their beneficial effects. It is unknown whether supplementation with PUFAs influences the production of SPMs. Alzheimer's disease (AD) is associated with brain inflammation and reduced levels of SPMs. The OmegAD study is a randomized, double-blind, and placebo-controlled clinical trial on AD patients, in which placebo or a supplement of 1.7 g DHA and 0.6 g EPA was taken daily for 6 months.
            Effects of n-3 FA supplementation on the release of proresolving lipid mediators by blood mononuclear cells: the OmegAD study[S]
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