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Vitamin Status in Children with Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutation

Background: The issue of vitamin metabolism in children with cystic fibrosis screen positive, inconclusive diagnosis (CFSPID) is not well known. The aim of this study was to determine the status of vitamins A, D, E, and C in the blood of a group of children with CFSPID. Material and Methods: A total...

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Autores principales: Wysocka-Wojakiewicz, Paulina, Woś, Halina, Wielkoszyński, Tomasz, Pyziak-Skupień, Aleksandra, Grzybowska-Chlebowczyk, Urszula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9654413/
https://www.ncbi.nlm.nih.gov/pubmed/36364923
http://dx.doi.org/10.3390/nu14214661
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author Wysocka-Wojakiewicz, Paulina
Woś, Halina
Wielkoszyński, Tomasz
Pyziak-Skupień, Aleksandra
Grzybowska-Chlebowczyk, Urszula
author_facet Wysocka-Wojakiewicz, Paulina
Woś, Halina
Wielkoszyński, Tomasz
Pyziak-Skupień, Aleksandra
Grzybowska-Chlebowczyk, Urszula
author_sort Wysocka-Wojakiewicz, Paulina
collection PubMed
description Background: The issue of vitamin metabolism in children with cystic fibrosis screen positive, inconclusive diagnosis (CFSPID) is not well known. The aim of this study was to determine the status of vitamins A, D, E, and C in the blood of a group of children with CFSPID. Material and Methods: A total of 89 children were enrolled in the study (Me: 3.6 years, 52.8% boys), as follows: 28 with CFSPID, 31 with CF (cystic fibrosis), and 30 HC (healthy children). Their blood concentrations of vitamins A, D, E, and C, and their dietary intake of these vitamins were analysed in the study groups on the basis of a three-day food diary. Results: The patients with CFSPID had significantly higher serum vitamin D (p = 0.01) and E (p = 0.04) concentrations, compared to the children with CF. None of the children with CFSPID revealed vitamin A or E deficiencies. Patients with CF had been consuming significantly higher vitamin D and E amounts (p = 0.01). The vitamin concentrations did not depend either on the pancreatic/liver function or on anthropometric parameters. In total, 32.14% of patients with CF did not cover the baseline recommended calorie intake, and 53.6% and 36% did not take the recommended vitamin E and vitamin A intake, respectively. Conclusion: Children with CF and CFSPID did not fully cover the dietary recommendations for vitamin supply, but vitamin deficiency was found only in CF.
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spelling pubmed-96544132022-11-15 Vitamin Status in Children with Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutation Wysocka-Wojakiewicz, Paulina Woś, Halina Wielkoszyński, Tomasz Pyziak-Skupień, Aleksandra Grzybowska-Chlebowczyk, Urszula Nutrients Article Background: The issue of vitamin metabolism in children with cystic fibrosis screen positive, inconclusive diagnosis (CFSPID) is not well known. The aim of this study was to determine the status of vitamins A, D, E, and C in the blood of a group of children with CFSPID. Material and Methods: A total of 89 children were enrolled in the study (Me: 3.6 years, 52.8% boys), as follows: 28 with CFSPID, 31 with CF (cystic fibrosis), and 30 HC (healthy children). Their blood concentrations of vitamins A, D, E, and C, and their dietary intake of these vitamins were analysed in the study groups on the basis of a three-day food diary. Results: The patients with CFSPID had significantly higher serum vitamin D (p = 0.01) and E (p = 0.04) concentrations, compared to the children with CF. None of the children with CFSPID revealed vitamin A or E deficiencies. Patients with CF had been consuming significantly higher vitamin D and E amounts (p = 0.01). The vitamin concentrations did not depend either on the pancreatic/liver function or on anthropometric parameters. In total, 32.14% of patients with CF did not cover the baseline recommended calorie intake, and 53.6% and 36% did not take the recommended vitamin E and vitamin A intake, respectively. Conclusion: Children with CF and CFSPID did not fully cover the dietary recommendations for vitamin supply, but vitamin deficiency was found only in CF. MDPI 2022-11-04 /pmc/articles/PMC9654413/ /pubmed/36364923 http://dx.doi.org/10.3390/nu14214661 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wysocka-Wojakiewicz, Paulina
Woś, Halina
Wielkoszyński, Tomasz
Pyziak-Skupień, Aleksandra
Grzybowska-Chlebowczyk, Urszula
Vitamin Status in Children with Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutation
title Vitamin Status in Children with Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutation
title_full Vitamin Status in Children with Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutation
title_fullStr Vitamin Status in Children with Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutation
title_full_unstemmed Vitamin Status in Children with Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutation
title_short Vitamin Status in Children with Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutation
title_sort vitamin status in children with cystic fibrosis transmembrane conductance regulator gene mutation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9654413/
https://www.ncbi.nlm.nih.gov/pubmed/36364923
http://dx.doi.org/10.3390/nu14214661
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