Vitamins A, D, E status as related to supplementation and lung disease markers in young children with cystic fibrosis.


Journal

Pediatric pulmonology
ISSN: 1099-0496
Titre abrégé: Pediatr Pulmonol
Pays: United States
ID NLM: 8510590

Informations de publication

Date de publication:
04 2022
Historique:
revised: 22 12 2021
received: 02 09 2021
accepted: 08 01 2022
pubmed: 13 1 2022
medline: 3 5 2022
entrez: 12 1 2022
Statut: ppublish

Résumé

The variable response to fat-soluble vitamin supplementation in young children with cystic fibrosis (CF), and factors contributing to this variability, remain under-investigated. 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. 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. 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. 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.

Sections du résumé

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.

Identifiants

pubmed: 35018747
doi: 10.1002/ppul.25825
pmc: PMC8930603
mid: NIHMS1772130
doi:

Substances chimiques

Interleukin-8 0
Vitamins 0
Vitamin A 11103-57-4
Interleukin-10 130068-27-8
Vitamin D 1406-16-2
Vitamin E 1406-18-4
alpha-Tocopherol H4N855PNZ1

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

935-944

Subventions

Organisme : NIDDK NIH HHS
ID : R56 DK109692
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK109692
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK072126
Pays : United States

Informations de copyright

© 2022 Wiley Periodicals LLC.

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Auteurs

HuiChuan J Lai (HJ)

Department of Nutritional Sciences, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Department of Pediatrics, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Lyanne H Chin (LH)

Department of Nutritional Sciences, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Sangita Murali (S)

Department of Nutritional Sciences, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Taiya Bach (T)

Department of Nutritional Sciences, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Danielle Sander (D)

Department of Nutritional Sciences, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Philip M Farrell (PM)

Department of Pediatrics, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Department of Population Health Sciences, University of Wisconsin-Madison, Madison, Wisconsin, USA.

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Classifications MeSH