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Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice

BACKGROUND: Hepatorenal tyrosinaemia (Tyr 1) is a rare inborn error of tyrosine metabolism. Without treatment, patients are at high risk of developing acute liver failure, renal dysfunction and in the long run hepatocellular carcinoma. The aim of our study was to collect cross-sectional data. METHOD...

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Autores principales: Mayorandan, Sebene, Meyer, Uta, Gokcay, Gülden, Segarra, Nuria Garcia, de Baulny, Hélène Ogier, van Spronsen, Francjan, Zeman, Jiri, de Laet, Corinne, Spiekerkoetter, Ute, Thimm, Eva, Maiorana, Arianna, Dionisi-Vici, Carlo, Moeslinger, Dorothea, Brunner-Krainz, Michaela, Lotz-Havla, Amelie Sophia, Cocho de Juan, José Angel, Couce Pico, Maria Luz, Santer, René, Scholl-Bürgi, Sabine, Mandel, Hanna, Bliksrud, Yngve Thomas, Freisinger, Peter, Aldamiz-Echevarria, Luis Jose, Hochuli, Michel, Gautschi, Matthias, Endig, Jessica, Jordan, Jens, McKiernan, Patrick, Ernst, Stefanie, Morlot, Susanne, Vogel, Arndt, Sander, Johannes, Das, Anibh Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4347563/
https://www.ncbi.nlm.nih.gov/pubmed/25081276
http://dx.doi.org/10.1186/s13023-014-0107-7
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author Mayorandan, Sebene
Meyer, Uta
Gokcay, Gülden
Segarra, Nuria Garcia
de Baulny, Hélène Ogier
van Spronsen, Francjan
Zeman, Jiri
de Laet, Corinne
Spiekerkoetter, Ute
Thimm, Eva
Maiorana, Arianna
Dionisi-Vici, Carlo
Moeslinger, Dorothea
Brunner-Krainz, Michaela
Lotz-Havla, Amelie Sophia
Cocho de Juan, José Angel
Couce Pico, Maria Luz
Santer, René
Scholl-Bürgi, Sabine
Mandel, Hanna
Bliksrud, Yngve Thomas
Freisinger, Peter
Aldamiz-Echevarria, Luis Jose
Hochuli, Michel
Gautschi, Matthias
Endig, Jessica
Jordan, Jens
McKiernan, Patrick
Ernst, Stefanie
Morlot, Susanne
Vogel, Arndt
Sander, Johannes
Das, Anibh Martin
author_facet Mayorandan, Sebene
Meyer, Uta
Gokcay, Gülden
Segarra, Nuria Garcia
de Baulny, Hélène Ogier
van Spronsen, Francjan
Zeman, Jiri
de Laet, Corinne
Spiekerkoetter, Ute
Thimm, Eva
Maiorana, Arianna
Dionisi-Vici, Carlo
Moeslinger, Dorothea
Brunner-Krainz, Michaela
Lotz-Havla, Amelie Sophia
Cocho de Juan, José Angel
Couce Pico, Maria Luz
Santer, René
Scholl-Bürgi, Sabine
Mandel, Hanna
Bliksrud, Yngve Thomas
Freisinger, Peter
Aldamiz-Echevarria, Luis Jose
Hochuli, Michel
Gautschi, Matthias
Endig, Jessica
Jordan, Jens
McKiernan, Patrick
Ernst, Stefanie
Morlot, Susanne
Vogel, Arndt
Sander, Johannes
Das, Anibh Martin
author_sort Mayorandan, Sebene
collection PubMed
description BACKGROUND: Hepatorenal tyrosinaemia (Tyr 1) is a rare inborn error of tyrosine metabolism. Without treatment, patients are at high risk of developing acute liver failure, renal dysfunction and in the long run hepatocellular carcinoma. The aim of our study was to collect cross-sectional data. METHODS: Via questionnaires we collected retrospective data of 168 patients with Tyr 1 from 21 centres (Europe, Turkey and Israel) about diagnosis, treatment, monitoring and outcome. In a subsequent consensus workshop, we discussed data and clinical implications. RESULTS: Early treatment by NTBC accompanied by diet is essential to prevent serious complications such as liver failure, hepatocellular carcinoma and renal disease. As patients may remain initially asymptomatic or develop uncharacteristic clinical symptoms in the first months of life newborn mass screening using succinylacetone (SA) as a screening parameter in dried blood is mandatory for early diagnosis. NTBC-treatment has to be combined with natural protein restriction supplemented with essential amino acids. NTBC dosage should be reduced to the minimal dose allowing metabolic control, once daily dosing may be an option in older children and adults in order to increase compliance. Metabolic control is judged by SA (below detection limit) in dried blood or urine, plasma tyrosine (<400 μM) and NTBC-levels in the therapeutic range (20–40 μM). Side effects of NTBC are mild and often transient. Indications for liver transplantation are hepatocellular carcinoma or failure to respond to NTBC. Follow-up procedures should include liver and kidney function tests, tumor markers and imaging, ophthalmological examination, blood count, psychomotor and intelligence testing as well as therapeutic monitoring (SA, tyrosine, NTBC in blood). CONCLUSION: Based on the data from 21 centres treating 168 patients we were able to characterize current practice and clinical experience in Tyr 1. This information could form the basis for clinical practice recommendations, however further prospective data are required to underpin some of the recommendations.
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spelling pubmed-43475632015-03-04 Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice Mayorandan, Sebene Meyer, Uta Gokcay, Gülden Segarra, Nuria Garcia de Baulny, Hélène Ogier van Spronsen, Francjan Zeman, Jiri de Laet, Corinne Spiekerkoetter, Ute Thimm, Eva Maiorana, Arianna Dionisi-Vici, Carlo Moeslinger, Dorothea Brunner-Krainz, Michaela Lotz-Havla, Amelie Sophia Cocho de Juan, José Angel Couce Pico, Maria Luz Santer, René Scholl-Bürgi, Sabine Mandel, Hanna Bliksrud, Yngve Thomas Freisinger, Peter Aldamiz-Echevarria, Luis Jose Hochuli, Michel Gautschi, Matthias Endig, Jessica Jordan, Jens McKiernan, Patrick Ernst, Stefanie Morlot, Susanne Vogel, Arndt Sander, Johannes Das, Anibh Martin Orphanet J Rare Dis Research BACKGROUND: Hepatorenal tyrosinaemia (Tyr 1) is a rare inborn error of tyrosine metabolism. Without treatment, patients are at high risk of developing acute liver failure, renal dysfunction and in the long run hepatocellular carcinoma. The aim of our study was to collect cross-sectional data. METHODS: Via questionnaires we collected retrospective data of 168 patients with Tyr 1 from 21 centres (Europe, Turkey and Israel) about diagnosis, treatment, monitoring and outcome. In a subsequent consensus workshop, we discussed data and clinical implications. RESULTS: Early treatment by NTBC accompanied by diet is essential to prevent serious complications such as liver failure, hepatocellular carcinoma and renal disease. As patients may remain initially asymptomatic or develop uncharacteristic clinical symptoms in the first months of life newborn mass screening using succinylacetone (SA) as a screening parameter in dried blood is mandatory for early diagnosis. NTBC-treatment has to be combined with natural protein restriction supplemented with essential amino acids. NTBC dosage should be reduced to the minimal dose allowing metabolic control, once daily dosing may be an option in older children and adults in order to increase compliance. Metabolic control is judged by SA (below detection limit) in dried blood or urine, plasma tyrosine (<400 μM) and NTBC-levels in the therapeutic range (20–40 μM). Side effects of NTBC are mild and often transient. Indications for liver transplantation are hepatocellular carcinoma or failure to respond to NTBC. Follow-up procedures should include liver and kidney function tests, tumor markers and imaging, ophthalmological examination, blood count, psychomotor and intelligence testing as well as therapeutic monitoring (SA, tyrosine, NTBC in blood). CONCLUSION: Based on the data from 21 centres treating 168 patients we were able to characterize current practice and clinical experience in Tyr 1. This information could form the basis for clinical practice recommendations, however further prospective data are required to underpin some of the recommendations. BioMed Central 2014-08-01 /pmc/articles/PMC4347563/ /pubmed/25081276 http://dx.doi.org/10.1186/s13023-014-0107-7 Text en Copyright © 2014 Mayorandan et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Mayorandan, Sebene
Meyer, Uta
Gokcay, Gülden
Segarra, Nuria Garcia
de Baulny, Hélène Ogier
van Spronsen, Francjan
Zeman, Jiri
de Laet, Corinne
Spiekerkoetter, Ute
Thimm, Eva
Maiorana, Arianna
Dionisi-Vici, Carlo
Moeslinger, Dorothea
Brunner-Krainz, Michaela
Lotz-Havla, Amelie Sophia
Cocho de Juan, José Angel
Couce Pico, Maria Luz
Santer, René
Scholl-Bürgi, Sabine
Mandel, Hanna
Bliksrud, Yngve Thomas
Freisinger, Peter
Aldamiz-Echevarria, Luis Jose
Hochuli, Michel
Gautschi, Matthias
Endig, Jessica
Jordan, Jens
McKiernan, Patrick
Ernst, Stefanie
Morlot, Susanne
Vogel, Arndt
Sander, Johannes
Das, Anibh Martin
Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice
title Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice
title_full Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice
title_fullStr Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice
title_full_unstemmed Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice
title_short Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice
title_sort cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4347563/
https://www.ncbi.nlm.nih.gov/pubmed/25081276
http://dx.doi.org/10.1186/s13023-014-0107-7
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