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Peer-reviewed veterinary case report

Oral vitamin E absorption in English Cocker Spaniels with familial vitamin E deficiency and retinal pigment epithelial dystrophy.

Journal:
Veterinary ophthalmology
Year:
2012
Authors:
McLellan, Gillian J & Bedford, Peter G C
Affiliation:
Department of Small Animal Medicine and Surgery · United Kingdom
Species:
dog

Abstract

BACKGROUND: Retinal Pigment Epithelial Dystrophy (RPED) with neuroaxonal degeneration in English Cocker Spaniels (ECS) is associated with systemic vitamin E deficiency in the absence of dietary insufficiency. OBJECTIVE: To evaluate the ability of ECS with RPED to absorb orally administered vitamin E and establish a basis for vitamin E supplementation in affected dogs. ANIMALS STUDIED: 8 RPED-affected ECS and five clinically normal dogs. PROCEDURES: An oral vitamin E tolerance test (OVETT) was conducted in each dog. Blood samples were obtained prior to and at 3, 6, 9, 12, 24, 120, and 240 h following oral administration of 90 iu/kg of RRR-&#x3b1;-tocopherol. Plasma alpha tocopherol (&#x3b1;TOC) content was measured by normal phase, high-performance liquid chromatography, and indices of vitamin E absorption calculated. RESULTS: There was marked variation in OVETT results between individuals. In RPED-affected ECS, mean peak plasma &#x3b1;TOC concentration (17.87 &#xb1; 13.21 &#x3bc;g/mL), attained after administration of a large oral dose of the vitamin, was significantly lower than the mean peak plasma &#x3b1;TOC concentration attained in normal dogs (47.61 &#xb1; 17.17 &#x3bc;g/mL; P < 0.005). However, the plasma concentrations achieved in 7/8 RPED-affected dogs remained within the normal reference range for plasma &#x3b1;TOC in vitamin E-replete dogs, for at least 12 h postdose. CONCLUSIONS: Vitamin E-deficient ECS with RPED are capable of absorbing orally administered vitamin E. Twice daily administration of 600-900 iu tocopherol is likely to restore plasma vitamin E concentrations to the normal range in most affected dogs.

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Original publication: https://pubmed.ncbi.nlm.nih.gov/22831287/