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

      Lipid and metabolic syndrome traits in coronary artery disease: a Mendelian randomization study

      Journal of Lipid Research
      Vol. 62100044Published online: February 5, 2021
      • David G. Thomas
      • Ying Wei
      • Alan R. Tall
      Cited in Scopus: 0
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        Mendelian randomization (MR) of lipid traits in CAD has provided evidence for causal associations of LDL-C and TGs in CAD, but many lipid trait genetic variants have pleiotropic effects on other cardiovascular risk factors that may bias MR associations. The goal of this study was to evaluate pleiotropic effects of lipid trait genetic variants and to account for these effects in MR of lipid traits in CAD. We performed multivariable MR using inverse variance-weighted and MR-Egger methods in large (n ≥ 300,000) GWAS datasets.
        Lipid and metabolic syndrome traits in coronary artery disease: a Mendelian randomization study
      • Patient-Oriented and Epidemiological Research
        Open Access

        WAT apoC-I secretion: role in delayed chylomicron clearance in vivo and ex vivo in WAT in obese subjects

        Journal of Lipid Research
        Vol. 57Issue 6p1074–1085Published online: April 3, 2016
        • Yannick Cyr
        • Hanny Wassef
        • Simon Bissonnette
        • Valerie Lamantia
        • Jean Davignon
        • May Faraj
        Cited in Scopus: 9
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          Reduced white adipose tissue (WAT) LPL activity delays plasma clearance of TG-rich lipoproteins (TRLs). We reported the secretion of apoC-I, an LPL inhibitor, from WAT ex vivo in women. Therefore we hypothesized that WAT-secreted apoC-I associates with reduced WAT LPL activity and TRL clearance. WAT apoC-I secretion averaged 86.9 ± 31.4 pmol/g/4 h and 74.1 ± 36.6 pmol/g/4 h in 28 women and 11 men with BMI ≥27 kg/m2, respectively, with no sex differences. Following the ingestion of a 13C-triolein-labeled high-fat meal, subjects with high WAT apoC-I secretion (above median) had delayed postprandial plasma clearance of dietary TRLs, assessed from plasma 13C-triolein-labeled TGs and apoB48.
          WAT apoC-I secretion: role in delayed chylomicron clearance in vivo and ex vivo in WAT in obese subjects[S]
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