Vitamins A, D, E status as related to supplementation and lung disease markers in young children with cystic fibrosis
Authors:
- HuiChuan J. LaiHLHuiChuan J. Lai
- Philip M. FarrellPFPhilip M. Farrell
- FIRST Study GroupFGFIRST Study Group
- 20 January 2022
- journal article
- research article
- Published by Wiley in Pediatric Pulmonology
- Vol. 57 (4) , 935-944
Abstract
Background: The variable response to fat‐soluble vitamin supplementation in young children with cystic fibrosis (CF), and factors contributing to this variability, remain under‐investigated.Objective: To determine if recommended supplement doses normalize serum vitamins A (retinol), D (25‐hydroxy‐vitamin D, 25OHD), and E (α‐tocopherol), and identify factors predictive of achieving sufficiency, in children with CF in the first 3 years of life.Design: We studied 144 infants born during 2012–2017 and diagnosed with CF through newborn screening. Serum retinol, 25OHD, α‐tocopherol and plasma cytokines interleukin (IL)‐6, IL‐8, IL‐10, and tumor necrosis factor (TNF)‐α were measured in early infancy and yearly thereafter. Vitamin supplement intakes and respiratory microbiology were assessed every 1–2 months in infancy and quarterly thereafter.Results: The prevalence of vitamin D insufficiency (<30 ng/ml) at all ages combined was significantly higher (22%) compared to vitamin A (<200 ng/ml, 3%) and vitamin E (<5 µg/ml, 5%). All children were vitamin A sufficient by age 2 years. Vitamin E insufficiency was rare. Only 42% were early responders of vitamin D and 17% remain insufficient despite high supplement intakes. IL‐6 was positively correlated, while IL‐8, IL‐10, and TNF‐α were negatively correlated, with retinol and 25OHD. Multiple regression analysis revealed that supplement dose, season, α‐tocopherol, pancreatic insufficiency, respiratory infections and IL‐10 were significant predictors of 25OHD.Conclusion: Diagnosis through newborn screening coupled with supplementation normalized serum retinol and α‐tocopherol in almost all infants with CF by age 3 years. However, response to vitamin D supplements in young children with CF occurred later and variably despite early and sustained supplementation.Keywords
Funding Information
- Cystic Fibrosis Foundation (LAI14A0, LAI15A0, LAI17A0)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK072126, R01DK109692)
This publication has 46 references indexed in Scilit:
- Heritability and seasonal variability of vitamin D concentrations in male twinsThe American Journal of Clinical Nutrition, 2010
- Cystic Fibrosis Foundation Evidence-Based Guidelines for Management of Infants with Cystic FibrosisThe Journal of Pediatrics, 2009
- Recovery of Birth WeightzScore Within 2 Years of Diagnosis Is Positively Associated With Pulmonary Status at 6 Years of Age in Children With Cystic FibrosisPediatrics, 2009
- Current Treatment Recommendations for Correcting Vitamin D Deficiency in Pediatric Patients with Cystic Fibrosis Are InadequateThe Journal of Pediatrics, 2008
- Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus ReportThe Journal of Pediatrics, 2008
- Vitamin D DeficiencyNew England Journal of Medicine, 2007
- Use of fecal elastase-1 to classify pancreatic status in patients with cystic fibrosisThe Journal of Pediatrics, 2004
- Pancreatic insufficiency, growth, and nutrition in infants identified by newborn screening as having cystic fibrosisThe Journal of Pediatrics, 1992
- EVALUATION OF VITAMIN E DEFICIENCY IN CHILDREN WITH LUNG DISEASE*Annals of the New York Academy of Sciences, 1982
- 25-Hydroxycholecalciferol levels in patients with cystic fibrosisThe Journal of Pediatrics, 1979