1967
DOI: 10.1093/ajcn/20.5.415
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Vitamin A, Vitamin E, and Lipids in Serum of Children with Cystic Fibrosis or Congenital Heart Defects Compared with Normal Children

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Cited by 46 publications
(18 citation statements)
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“…Our data suggest that in children with CFP there is a defect in the ability to mobilize vitamin A from hepatic cells, perhaps owing to an inability to release retinol or to an inability to provide the transport proteins. This interpretation is consistent with reports that blood levels in CFP patients do rise after vitamin A absorption tests, but are not maintained at normal levels in spite of prolonged supplementation at high dosages [3].…”
Section: Discussionsupporting
confidence: 92%
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“…Our data suggest that in children with CFP there is a defect in the ability to mobilize vitamin A from hepatic cells, perhaps owing to an inability to release retinol or to an inability to provide the transport proteins. This interpretation is consistent with reports that blood levels in CFP patients do rise after vitamin A absorption tests, but are not maintained at normal levels in spite of prolonged supplementation at high dosages [3].…”
Section: Discussionsupporting
confidence: 92%
“…The ratio of the levels of u-tocopherol in plasma and tissue was constant, suggesting that both tissues were depleted in parallel. These low plasma values are similar to those reported by others for children with CFP [3,12,16] and probably reflect malabsorption. Several patients received 5 mg/kg/day of a water-dispersible vitamin E preparation for 4-1 1 months and exhibited an increase in plasma values in most cases, but the values usually remained below normal.…”
Section: Discussionsupporting
confidence: 91%
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“…Micelle formation is required for the absorption of vitamin E (57, 171). Pancreatic enzymes may also aid in its absorption (121); this is suggested by the finding of vitamin E deficiency in patients with cystic fibrosis, who do not secrete pancreatic enzymes (12,48,70,172,193).…”
Section: Vitamin Ementioning
confidence: 99%