Abstract
• Background: Vitamin A deficiency with eye symptoms has been reported in patients with cystic fibrosis who received the recommended daily intake of vitamin A. • Methods: We measured serum retinol, dark adaptation, contrast sensitivity, and dry eye status in 35 adult cystic fibrosis patients to ascertain whether they had ocular signs or symptons. • Results: Median serum retinol concentration was 1.95 μmol/l, range 1.08–4.01 μmol/l, with no values indicating vitamin A deficiency. Retinal light sensitivity was normal. Nineteen patients had reduced contrast sensitivity. Conjunctival imprints all showed plenty of goblet cells, but were characteristic of dry eye in 42% of patients (n=14). Decreased tear film stability was found in 49% (n=17), tear production was low in 31% (n=11), and 23% (n=8) showed an increased amount of dying epithelial cells. Nine patients (26%) had keratocon-junctivitis sicca according to the Copenhagen criteria. • Conclusion: Our patients had no biochemical or clinical signs of vitamin A deficiency. We speculate that the high incidence of dry eye could be a primary manifestation of cystic fibrosis.
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Morkeberg, J.C., Edmund, C., Prause, J.U. et al. Ocular findings in cystic fibrosis patients receiving vitamin A supplementation. Graefe's Arch Clin Exp Ophthalmol 233, 709–713 (1995). https://doi.org/10.1007/BF00164674
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DOI: https://doi.org/10.1007/BF00164674