Journal of Lipid Research (Oct 1997)

Effect of 360His mutation in apolipoprotein A-IV on plasma HDL-cholesterol response to dietary fat

  • S Jansen,
  • J Lopez-Miranda,
  • J M Ordovas,
  • J L Zambrana,
  • C Marin,
  • M A Ostos,
  • P Castro,
  • R McPherson,
  • F Lopez Segura,
  • A Blanco,
  • J A Jimenez Pereperez,
  • F Perez-Jimenez

Journal volume & issue
Vol. 38, no. 10
pp. 1995 – 2002

Abstract

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In order to determine whether genetic variability of apolipoprotein (apo) A-IV is responsible for the improvement in lipid profile when dietary saturated fats are replaced by carbohydrates or monounsaturated fats, 41 healthy male subjects were studied: 33 were homozygous for the 360Gln allele and 8 were heterozygote carriers of the 360His allele. These were administered three consecutive 4-week diets. The first was a diet rich in saturated fat (SAT diet, with 38﹪ fat, 20﹪ saturated. This was followed by a low fat diet (NCEP-I, with < 30﹪ fat, < ﹪ saturated). The final diet was rich in monounsaturated fat (MUFA diet, with ﹪ fat, 22﹪ monounsaturated). There was no difference in plasma lipid and apolipoprotein levels of both groups of individuals after consuming the SAT diet. Switching from this diet to the NCEP-I diet, carriers of the 360His allele presented a greater decrease in high density lipoprotein-cholesterol (HDL-C) (-10 vs. -1 mg/dL, P < 0.004) and apoA-I levels (-19 vs. -8 mg/dL, P < 0.037). Similarly, replacement of carbohydrates by monounsaturated fats produced a greater increase in HDL-C (9 vs. 1 mg/dL, P < 0.003) and apoA-I levels (9 vs. 2 mg/dL, P < 0.036) in carriers of the 360His mutation. Lecithin:cholesterol acyltransferase (LCAT) and cholesteryl ester transfer protein (CETP) activities and apoA-IV levels were also measured. However, no genotype-related differences were observed for these parameters. Our results suggest that variability in HDL-C and apoA-I response to diet is, at least partially, determined by the 360His mutation of apoA-IV.