Journal of Lipid Research (Sep 2018)

Efficacy of two vitamin E formulations in patients with abetalipoproteinemia and chylomicron retention disease

  • Charlotte Cuerq,
  • Emilie Henin,
  • Lioara Restier,
  • Emilie Blond,
  • Jocelyne Drai,
  • Christophe Marçais,
  • Mathilde Di Filippo,
  • Christian Laveille,
  • Marie-Caroline Michalski,
  • Pierre Poinsot,
  • Cyrielle Caussy,
  • Agnès Sassolas,
  • Philippe Moulin,
  • Emmanuelle Reboul,
  • Sybil Charriere,
  • Emile Levy,
  • Alain Lachaux,
  • Noël Peretti

Journal volume & issue
Vol. 59, no. 9
pp. 1640 – 1648

Abstract

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Abetalipoproteinemia (ABL) and chylomicron retention disease (CMRD) are extremely rare recessive forms of hypobetalipoproteinemia characterized by intestinal lipid malabsorption and severe vitamin E deficiency. Vitamin E is often supplemented in the form of fat-soluble vitamin E acetate, but fat malabsorption considerably limits correction of the deficiency. In this crossover study, we administered two different forms of vitamin E, tocofersolan (a water-soluble derivative of RRR-α-tocopherol) and α-tocopherol acetate, to three patients with ABL and four patients with CMRD. The aims of this study were to evaluate the intestinal absorption characteristics of tocofersolan versus α-tocopherol acetate by measuring the plasma concentrations of α-tocopherol over time after a single oral load and to compare efficacy by evaluating the ability of each formulation to restore vitamin E storage after 4 months of treatment. In patients with ABL, tocofersolan and α-tocopherol acetate bioavailabilities were extremely low (2.8% and 3.1%, respectively). In contrast, bioavailabilities were higher in patients with CMRD (tocofersolan, 24.7%; α-tocopherol acetate, 11.4%). Plasma concentrations of α-tocopherol at 4 months were not significantly different by formulation type in ABL or CMRD. This study provides new insights about vitamin E status in ABL and CMRD and suggests the potential of different formulations as treatment options.

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