| Literature DB >> 30021760 |
Charlotte Cuerq1, Emilie Henin2, Lioara Restier3, Emilie Blond1, Jocelyne Drai1, Christophe Marçais1, Mathilde Di Filippo4, Christian Laveille2, Marie-Caroline Michalski5, Pierre Poinsot3, Cyrielle Caussy5, Agnès Sassolas4, Philippe Moulin6, Emmanuelle Reboul7, Sybil Charriere6, Emile Levy8, Alain Lachaux9, Noël Peretti10.
Abstract
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.Entities:
Keywords: Anderson disease; absorption; adipose tissue; hypocholesterolemia; lipid and lipoprotein metabolism; metabolic disease; tocopherol
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Year: 2018 PMID: 30021760 PMCID: PMC6121919 DOI: 10.1194/jlr.M085043
Source DB: PubMed Journal: J Lipid Res ISSN: 0022-2275 Impact factor: 5.922