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Journal of Lipid Research
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    • high density lipoprotein2
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    JLR Patient-Oriented and Epidemiological Research

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    • Patient-Oriented and Epidemiological Research
      Open Access

      A genome-wide search for gene-by-obesity interaction loci of dyslipidemia in Koreans shows diverse genetic risk alleles

      Journal of Lipid Research
      Vol. 60Issue 12p2090–2101Published online: October 29, 2019
      • Moonil Kang
      • Joohon Sung
      Cited in Scopus: 2
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        Dyslipidemia is a well-established risk factor for CVD. Studies suggest that similar fat accumulation in a given population might result in different levels of dyslipidemia risk among individuals; for example, despite similar or leaner body composition compared with Caucasians, Asians of Korean descent experience a higher prevalence of dyslipidemia. These variations imply a possible role of gene-obesity interactions on lipid profiles. Genome-wide association studies have identified more than 500 loci regulating plasma lipids, but the interaction structure between genes and obesity traits remains unclear.
        A genome-wide search for gene-by-obesity interaction loci of dyslipidemia in Koreans shows diverse genetic risk alleles
      • Patient-Oriented and Epidemiological Research
        Open Access

        Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population

        Journal of Lipid Research
        Vol. 59Issue 10p1951–1966Published online: August 14, 2018
        • Prashantha Hebbar
        • Rasheeba Nizam
        • Motasem Melhem
        • Fadi Alkayal
        • Naser Elkum
        • Sumi Elsa John
        • and others
        Cited in Scopus: 14
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          Abnormal blood lipid levels are influenced by genetic and lifestyle/dietary factors. Although many genetic variants associated with blood lipid traits have been identified in Europeans, similar data in Middle Eastern populations are limited. We performed a genome-wide association study with Arab individuals (discovery cohort: 1,353; replication cohort: 1,176) from Kuwait to identify possible associations of genetic variants with high lipid levels. We used Illumina HumanOmniExpress BeadChip and candidate SNP genotyping in the discovery and replication phases, respectively.
          Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population
        • 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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