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

      Higher chylomicron remnants and LDL particle numbers associate with CD36 SNPs and DNA methylation sites that reduce CD36

      Journal of Lipid Research
      Vol. 57Issue 12p2176–2184Published online: October 11, 2016
      • Latisha Love-Gregory
      • Aldi T. Kraja
      • Fiona Allum
      • Stella Aslibekyan
      • Åsa K. Hedman
      • Yanan Duan
      • and others
      Cited in Scopus: 23
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        Cluster of differentiation 36 (CD36) variants influence fasting lipids and risk of metabolic syndrome, but their impact on postprandial lipids, an independent risk factor for cardiovascular disease, is unclear. We determined the effects of SNPs within a ∼410 kb region encompassing CD36 and its proximal and distal promoters on chylomicron (CM) remnants and LDL particles at fasting and at 3.5 and 6 h following a high-fat meal (Genetics of Lipid Lowering Drugs and Diet Network study, n = 1,117). Five promoter variants associated with CMs, four with delayed TG clearance and five with LDL particle number.
        Higher chylomicron remnants and LDL particle numbers associate with CD36 SNPs and DNA methylation sites that reduce CD36[S]
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