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

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

Edité par CCSD ; American Society for Biochemistry and Molecular Biology -

International audience. 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-alpha-tocopherol) and alpha-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 alpha-tocopherol acetate by measuring the plasma concentrations of alpha-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 alpha-tocopherol acetate bioavailabilities were extremely low (2.8% and 3.1%, respectively). In contrast, bioavailabilities were higher in patients with CMRD (tocofersolan, 24.7%; alpha-tocopherol acetate, 11.4%). Plasma concentrations of alpha-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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