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

      Does pregnancy alter life-course lipid trajectories? Evidence from the HUNT Study in Norway

      Journal of Lipid Research
      Vol. 59Issue 12p2403–2412Published online: October 12, 2018
      • Amanda R. Markovitz
      • Eirin B. Haug
      • Julie Horn
      • Abigail Fraser
      • Corrie Macdonald-Wallis
      • Kate Tilling
      • and others
      Cited in Scopus: 11
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        We examined the association between pregnancy and life-course lipid trajectories. Linked data from the Nord-Trøndelag Health Study and the Medical Birth Registry of Norway yielded 19,987 parous and 1,625 nulliparous women. Using mixed-effects spline models, we estimated differences in nonfasting lipid levels from before to after first birth in parous women and between parous and nulliparous women. HDL cholesterol (HDL-C) dropped by −4.2 mg/dl (95% CI: −5.0, −3.3) from before to after first birth in adjusted models, a 7% change, and the total cholesterol (TC) to HDL-C ratio increased by 0.18 (95% CI: 0.11, 0.25), with no change in non-HDL-C or triglycerides.
        Does pregnancy alter life-course lipid trajectories? Evidence from the HUNT Study in Norway
      • Patient-Oriented and Epidemiological Research
        Open Access

        Effect of adding bezafibrate to standard lipid-lowering therapy on post-fat load lipid levels in patients with familial dysbetalipoproteinemia. A randomized placebo-controlled crossover trial

        Journal of Lipid Research
        Vol. 58Issue 11p2180–2187Published online: September 19, 2017
        • Charlotte Koopal
        • A. David Marais
        • Jan Westerink
        • Yolanda van der Graaf
        • Frank L.J. Visseren
        Cited in Scopus: 15
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          Familial dysbetalipoproteinemia (FD) is a genetic disorder associated with impaired postprandial lipid clearance. The effect of adding bezafibrate to standard lipid-lowering therapy on postprandial and fasting lipid levels in patients with FD is unknown. In this randomized placebo-controlled double-blind crossover trial, 15 patients with FD received bezafibrate and placebo for 6 weeks in randomized order in addition to standard lipid-lowering therapy (statin, ezetimibe, and/or lifestyle). We assessed post-fat load lipids, expressed as incremental area under the curve (iAUC) and area under the curve (AUC), as well as fasting levels and safety, and found that adding bezafibrate did not reduce post-fat load non-HDL-cholesterol (non-HDL-C) iAUC (1.78 ± 4.49 mmol·h/l vs.
          Effect of adding bezafibrate to standard lipid-lowering therapy on post-fat load lipid levels in patients with familial dysbetalipoproteinemia. A randomized placebo-controlled crossover trial
        • Patient-Oriented and Epidemiological Research
          Open Access

          Associations of genetic variants for adult lipid levels with lipid levels in children. The Generation R Study

          Journal of Lipid Research
          Vol. 57Issue 12p2185–2192Published online: October 24, 2016
          • Ardashel Latsuzbaia
          • Vincent W.V. Jaddoe
          • Albert Hofman
          • Oscar H. Franco
          • Janine F. Felix
          Cited in Scopus: 7
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            Lipid concentrations are heritable traits. Recently, the number of known genetic loci associated with lipid levels in adults increased from 95 to 157. The effects of these 157 loci have not been tested in children. Considering that lipid levels track from childhood to adulthood, we studied to determine whether these variants already affected lipid concentrations in a large group of 2,645 children with a median age of 6.0 years (95% range 5.7–7.3 years) from the population-based Generation R Study.
            Associations of genetic variants for adult lipid levels with lipid levels in children. The Generation R Study[S]
          • Patient-Oriented and Epidemiological Research
            Open Access

            Levels of atherogenic lipoproteins are unexpectedly reduced in interstitial fluid from type 2 diabetes patients

            Journal of Lipid Research
            Vol. 56Issue 8p1633–1639Published online: June 19, 2015
            • Johanna Apro
            • Paolo Parini
            • Anders Broijersén
            • Bo Angelin
            • Mats Rudling
            Cited in Scopus: 6
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              At a given level of serum cholesterol, patients with T2D have an increased risk of developing atherosclerosis compared with nondiabetic subjects. We hypothesized that T2D patients have an increased interstitial fluid (IF)-to-serum gradient ratio for LDL, due to leakage over the vascular wall. Therefore, lipoprotein profiles in serum and IF from 35 T2D patients and 35 healthy controls were assayed using fast performance liquid chromatography. The IF-to-serum gradients for VLDL and LDL cholesterol, as well as for apoB, were clearly reduced in T2D patients compared with healthy controls.
              Levels of atherogenic lipoproteins are unexpectedly reduced in interstitial fluid from type 2 diabetes patients[S]
            • Patient-Oriented and Epidemiological Research
              Open Access

              Lipidomic changes of LDL in overweight and moderately hypercholesterolemic subjects taking phytosterol- and omega-3-supplemented milk

              Journal of Lipid Research
              Vol. 56Issue 5p1043–1056Published online: March 15, 2015
              • Teresa Padro
              • Gemma Vilahur
              • Joan Sánchez-Hernández
              • Marta Hernández
              • Rosa M. Antonijoan
              • Antonio Perez
              • and others
              Cited in Scopus: 21
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                The benefits of dietary phytosterols (PhySs) and long-chain n-3 PUFA (ω3) have been linked to their effects as cholesterol- and triglyceride (TGL)-lowering agents. However, it remains unknown whether these compounds have further metabolic effects on LDL lipid composition. Here, we studied the effects of PhyS- or ω3-supplemented low-fat milk (milk) on the LDL-lipidome. Overweight and moderately hypercholesterolemic subjects (n = 32) were enrolled in a two-arm longitudinal crossover study. Milk (250 ml/day), enriched with either 1.57 g PhyS or 375 mg ω3 (EPA + DHA), was given to the participants during two sequential 28 day intervention periods.
                Lipidomic changes of LDL in overweight and moderately hypercholesterolemic subjects taking phytosterol- and omega-3-supplemented milk
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