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Is Prolonged Copper Restriction Needed in Pediatric Wilson’s Disease?

BACKGROUND: Dietary copper restriction in Wilson’s disease is recommended mostly for 1 year or until showing normal liver enzymes. Little is known about the effect of long-term copper restriction on copper and nutritional status in the body. The relationship between daily copper consumption and seru...

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Autores principales: Hizarcıoğlu-Gülşen, Hayriye, Onat, Pınar Şimşek, Yıldırım, Damla, Demirtaş, Duygu, Boyraz, Meryem S., Göktaş, Mehmet A., Demir, Hülya, Özen, Hasan, Saltık-Temizel, İnci Nur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Turkish Society of Gastroenterology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9984943/
https://www.ncbi.nlm.nih.gov/pubmed/36511610
http://dx.doi.org/10.5152/tjg.2022.22216
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author Hizarcıoğlu-Gülşen, Hayriye
Onat, Pınar Şimşek
Yıldırım, Damla
Demirtaş, Duygu
Boyraz, Meryem S.
Göktaş, Mehmet A.
Demir, Hülya
Özen, Hasan
Saltık-Temizel, İnci Nur
author_facet Hizarcıoğlu-Gülşen, Hayriye
Onat, Pınar Şimşek
Yıldırım, Damla
Demirtaş, Duygu
Boyraz, Meryem S.
Göktaş, Mehmet A.
Demir, Hülya
Özen, Hasan
Saltık-Temizel, İnci Nur
author_sort Hizarcıoğlu-Gülşen, Hayriye
collection PubMed
description BACKGROUND: Dietary copper restriction in Wilson’s disease is recommended mostly for 1 year or until showing normal liver enzymes. Little is known about the effect of long-term copper restriction on copper and nutritional status in the body. The relationship between daily copper consumption and serum and urine copper parameters, liver enzymes, and dietary contents was investigated. METHODS: In this study, 32 pediatric Wilson’s disease patients who had been on treatment at least for 12 months were included. Clinical features, liver enzymes, serum total copper concentrations, non-ceruloplasmin bound copper concentrations, adjusted copper concentrations, 24-hour urine copper excretions, and macro- and micronutrient consumptions were analyzed. RESULTS: In total, 27 patients reported following copper-restricted diets, while daily copper consumption was low only in 7 patients (21.9%). Total copper concentrations and non-ceruloplasmin-bound copper concentrations were low at 78.1% and 53.1%, respectively. All but one adjusted copper concentration were within normal limits. Total copper concentrations, adjusted copper concentration, and non-ceruloplasmin-bound copper concentrations correlated with each other but none correlated with urine copper excretions. Daily copper consumption was inversely correlated with total copper concentrations (P = .041, r = –0.363) but not correlated with non-ceruloplasmin-bound copper concentrations and adjusted copper concentrations. There was no relationship between liver enzymes and daily copper consumption and serum and urine copper parameters. High fat consumption with low fiber and vitamin B6 was more common in low daily copper consumption group (P = .033, P = .029, P = .007, respectively). CONCLUSIONS: Daily copper consumption may be the least effective or non-effective factor on liver enzymes in Wilson’s disease. Prolonged copper restriction may result in unintentional dietary imbalance. Avoidance of undernutrition and high-fat meals, as well as enrichment of the meals with vitamin B6 and fiber, should be encouraged during copper-restricted diets.
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spelling pubmed-99849432023-03-05 Is Prolonged Copper Restriction Needed in Pediatric Wilson’s Disease? Hizarcıoğlu-Gülşen, Hayriye Onat, Pınar Şimşek Yıldırım, Damla Demirtaş, Duygu Boyraz, Meryem S. Göktaş, Mehmet A. Demir, Hülya Özen, Hasan Saltık-Temizel, İnci Nur Turk J Gastroenterol Original Article BACKGROUND: Dietary copper restriction in Wilson’s disease is recommended mostly for 1 year or until showing normal liver enzymes. Little is known about the effect of long-term copper restriction on copper and nutritional status in the body. The relationship between daily copper consumption and serum and urine copper parameters, liver enzymes, and dietary contents was investigated. METHODS: In this study, 32 pediatric Wilson’s disease patients who had been on treatment at least for 12 months were included. Clinical features, liver enzymes, serum total copper concentrations, non-ceruloplasmin bound copper concentrations, adjusted copper concentrations, 24-hour urine copper excretions, and macro- and micronutrient consumptions were analyzed. RESULTS: In total, 27 patients reported following copper-restricted diets, while daily copper consumption was low only in 7 patients (21.9%). Total copper concentrations and non-ceruloplasmin-bound copper concentrations were low at 78.1% and 53.1%, respectively. All but one adjusted copper concentration were within normal limits. Total copper concentrations, adjusted copper concentration, and non-ceruloplasmin-bound copper concentrations correlated with each other but none correlated with urine copper excretions. Daily copper consumption was inversely correlated with total copper concentrations (P = .041, r = –0.363) but not correlated with non-ceruloplasmin-bound copper concentrations and adjusted copper concentrations. There was no relationship between liver enzymes and daily copper consumption and serum and urine copper parameters. High fat consumption with low fiber and vitamin B6 was more common in low daily copper consumption group (P = .033, P = .029, P = .007, respectively). CONCLUSIONS: Daily copper consumption may be the least effective or non-effective factor on liver enzymes in Wilson’s disease. Prolonged copper restriction may result in unintentional dietary imbalance. Avoidance of undernutrition and high-fat meals, as well as enrichment of the meals with vitamin B6 and fiber, should be encouraged during copper-restricted diets. Turkish Society of Gastroenterology 2023-01-01 /pmc/articles/PMC9984943/ /pubmed/36511610 http://dx.doi.org/10.5152/tjg.2022.22216 Text en © Copyright 2023 authors https://creativecommons.org/licenses/by/4.0/ Content of this journal is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Original Article
Hizarcıoğlu-Gülşen, Hayriye
Onat, Pınar Şimşek
Yıldırım, Damla
Demirtaş, Duygu
Boyraz, Meryem S.
Göktaş, Mehmet A.
Demir, Hülya
Özen, Hasan
Saltık-Temizel, İnci Nur
Is Prolonged Copper Restriction Needed in Pediatric Wilson’s Disease?
title Is Prolonged Copper Restriction Needed in Pediatric Wilson’s Disease?
title_full Is Prolonged Copper Restriction Needed in Pediatric Wilson’s Disease?
title_fullStr Is Prolonged Copper Restriction Needed in Pediatric Wilson’s Disease?
title_full_unstemmed Is Prolonged Copper Restriction Needed in Pediatric Wilson’s Disease?
title_short Is Prolonged Copper Restriction Needed in Pediatric Wilson’s Disease?
title_sort is prolonged copper restriction needed in pediatric wilson’s disease?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9984943/
https://www.ncbi.nlm.nih.gov/pubmed/36511610
http://dx.doi.org/10.5152/tjg.2022.22216
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