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Vitamin D in infants with cystic fibrosis diagnosed by newborn screening
Liza A Neville1, Sarath C Ranganathan
1Department of Respiratory Medicine, Royal Children's Hospital, Melbourne Vic., Australia.
Insights
Vitamin D deficiency is common in infants with cystic fibrosis (CF) at diagnosis. Supplementation improves vitamin D levels over time, though initial deficiencies in vitamins A and E are linked to pancreatic insufficiency.
Area of Science:
- Pediatric Nutrition
- Cystic Fibrosis Research
- Nutritional Biochemistry
Background:
- Newborn screening identifies infants with cystic fibrosis (CF), enabling early detection of nutritional deficiencies.
- While vitamin E deficiency is rare in older CF patients, vitamin D status at diagnosis and its relation to other fat-soluble vitamins are not well-established.
Purpose of the Study:
- To determine vitamin D status in infants diagnosed with CF via newborn screening.
- To investigate the relationship between vitamin D levels and other fat-soluble vitamins (A and E), sex, birth month, and pancreatic status at diagnosis.
Main Methods:
- Retrospective review of vitamin levels in infants diagnosed with CF over a 5-year period.
- Measurement of vitamin D using radioimmunoassay and vitamins A and E using high-performance liquid chromatography.
- Statistical assessment of associations between vitamin D levels and demographic/clinical factors.
Main Results:
- Of 58 infants diagnosed, 30 had initial vitamin D levels assessed. Deficiencies were noted in 37% for vitamin D, 16% for vitamin E, and 60% for vitamin A.
- Vitamin D levels were not associated with sex, birth month, or pancreatic status, but were unrelated to vitamin A or E levels.
- Infants with pancreatic insufficiency had significantly lower vitamin A and E levels. Vitamin D levels improved with supplementation over time.
Conclusions:
- Vitamin D deficiency is prevalent in infants newly diagnosed with CF via newborn screening.
- Initial vitamin D deficiency is not linked to pancreatic status or low vitamin E levels.
- Vitamin D levels improve with treatment, indicating the effectiveness of supplementation strategies.
Aims:
Screening enables early nutritional deficiencies to be detected in those with cystic fibrosis (CF). Although vitamin deficiency is considered unlikely in older subjects with normal vitamin E levels, few studies have determined vitamin D status at diagnosis and its relationship to other fat-soluble vitamins.
Methods:
We reviewed vitamin levels in infants diagnosed with CF by newborn screening over a 5-year period in Melbourne, Australia. Vitamin D levels were determined using the IDS gamma-B 25-OH Vitamin D radio-immunoassay (Immunodiagnostic Systems Limited, Boldon, UK). Vitamins A and E were evaluated by high-performance liquid chromatography. We assessed the association between vitamin D level and sex, month of birth, pancreatic status, and vitamin A and E levels.
Results:
Fifty-eight infants were diagnosed at a median age of 1 month (range: 0-3 months). Initial vitamin D levels were assessed between 0.2 and 3.5 months in 30 (vitamin D) and 45 (vitamins A and E) infants. The number of infants deficient with vitamins D, E and A were 11 (37%), 7 (16%) and 27 (60%), respectively. Vitamin D levels were unrelated to sex, vitamin A or E levels, month of birth or pancreatic status, whereas vitamin A and E levels were significantly lower in those who were pancreatic insufficient. With supplementation, vitamin D increased over time.
Conclusions:
Vitamin D deficiency is common in infants newly diagnosed with CF by newborn screening and is unrelated to pancreatic status or predicted low vitamin E levels. Vitamin D deficiency is less common over time following treatment.
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