Skip to main content
Top
Published in: Orphanet Journal of Rare Diseases 1/2014

Open Access 01-12-2014 | Research

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

Authors: Sebene Mayorandan, Uta Meyer, Gülden Gokcay, Nuria Garcia Segarra, Hélène Ogier de Baulny, Francjan van Spronsen, Jiri Zeman, Corinne de Laet, Ute Spiekerkoetter, Eva Thimm, Arianna Maiorana, Carlo Dionisi-Vici, Dorothea Moeslinger, Michaela Brunner-Krainz, Amelie Sophia Lotz-Havla, José Angel Cocho de Juan, Maria Luz Couce Pico, René Santer, Sabine Scholl-Bürgi, Hanna Mandel, Yngve Thomas Bliksrud, Peter Freisinger, Luis Jose Aldamiz-Echevarria, Michel Hochuli, Matthias Gautschi, Jessica Endig, Jens Jordan, Patrick McKiernan, Stefanie Ernst, Susanne Morlot, Arndt Vogel, Johannes Sander, Anibh Martin Das

Published in: Orphanet Journal of Rare Diseases | Issue 1/2014

Login to get access

Abstract

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.
Appendix
Available only for authorised users
Literature
2.
go back to reference Chakrapani A, Holme E: Disorders of tyrosine metabolism. Inborn Metabolic diseases. 4th edition. Edited by: Fernandez S, Berghe W. 2006, Springer, Heidelberg, 233-243.CrossRef Chakrapani A, Holme E: Disorders of tyrosine metabolism. Inborn Metabolic diseases. 4th edition. Edited by: Fernandez S, Berghe W. 2006, Springer, Heidelberg, 233-243.CrossRef
3.
go back to reference Van Spronsen FJ, Bijleveld MA, van Maldegem BT, Wijburg FA: Hepatocellular Carcinoma in Hereditary Tyrosinemia Type I Despite 2-(2 Nitro-4-3-Trifluoro-Methylbenzoyl)-1,3-Cyclohexanedione Treatment. J Pedriatr Gastroenterol Nutr. 2005, 40: 90-93.CrossRef Van Spronsen FJ, Bijleveld MA, van Maldegem BT, Wijburg FA: Hepatocellular Carcinoma in Hereditary Tyrosinemia Type I Despite 2-(2 Nitro-4-3-Trifluoro-Methylbenzoyl)-1,3-Cyclohexanedione Treatment. J Pedriatr Gastroenterol Nutr. 2005, 40: 90-93.CrossRef
4.
go back to reference Weinberg AG, Mize CE, Worthen HG: The occurence of hepatoma in the chronic form of hereditary tyrosinemia. J Pediatr. 1976, 88: 434-438.CrossRefPubMed Weinberg AG, Mize CE, Worthen HG: The occurence of hepatoma in the chronic form of hereditary tyrosinemia. J Pediatr. 1976, 88: 434-438.CrossRefPubMed
5.
go back to reference Thimm E, Richter-Werkle R, Kamp G, Molke B, Herebian D, Klee D, Mayatepek E, Spiekerkoetter U: Neurocognitive outcome in patients with hypertyrosinemia type I after a long-term treatment with NTBC. J Inherit Metab Dis. 2012, 35: 263-268.CrossRefPubMed Thimm E, Richter-Werkle R, Kamp G, Molke B, Herebian D, Klee D, Mayatepek E, Spiekerkoetter U: Neurocognitive outcome in patients with hypertyrosinemia type I after a long-term treatment with NTBC. J Inherit Metab Dis. 2012, 35: 263-268.CrossRefPubMed
6.
go back to reference De Laet C, Munoz VT, Jaeken J, Francois B, Carton D, Sokal EM, Dan B, Goyens PJ: Neuropsychological outcome of NTBC-treated patients with tyrosinaemia type 1. Dev Med Child Neurol. 2011, 53: 962-964.CrossRefPubMed De Laet C, Munoz VT, Jaeken J, Francois B, Carton D, Sokal EM, Dan B, Goyens PJ: Neuropsychological outcome of NTBC-treated patients with tyrosinaemia type 1. Dev Med Child Neurol. 2011, 53: 962-964.CrossRefPubMed
7.
go back to reference Pohorecka M, Biernacka M, Jakubowska-Winecka A, Biernacki M, Kusmierska K, Kowalik A, Sykut-Cegielska J: Behavioral and intellectual functioning in patients with tyrosinemia type I. Pediatr Endocrinol Diabetes Metab. 2012, 18: 96-100.PubMed Pohorecka M, Biernacka M, Jakubowska-Winecka A, Biernacki M, Kusmierska K, Kowalik A, Sykut-Cegielska J: Behavioral and intellectual functioning in patients with tyrosinemia type I. Pediatr Endocrinol Diabetes Metab. 2012, 18: 96-100.PubMed
8.
go back to reference Bendadi F, de Koning TJ, Visser G, Prinsen HC, de Sain NG, Verhoeven-Duif N, Sinnema G, van Spronsen FJ, van Hasselt PM: Impaired cognitive functioning in patiens with tyrosinemia type I receiving nitisinone. J Pediatr. 2013, 164: 398-401.CrossRefPubMed Bendadi F, de Koning TJ, Visser G, Prinsen HC, de Sain NG, Verhoeven-Duif N, Sinnema G, van Spronsen FJ, van Hasselt PM: Impaired cognitive functioning in patiens with tyrosinemia type I receiving nitisinone. J Pediatr. 2013, 164: 398-401.CrossRefPubMed
9.
go back to reference Mustonen A, van Amstel HK P, Berger R, Salo MK, Viinikka L, Simola KOJ: Mutation analysis for prenatal diagnosis of hereditary tyrosianaemia type I. Prenat Diagn. 1997, 17: 964-966.CrossRefPubMed Mustonen A, van Amstel HK P, Berger R, Salo MK, Viinikka L, Simola KOJ: Mutation analysis for prenatal diagnosis of hereditary tyrosianaemia type I. Prenat Diagn. 1997, 17: 964-966.CrossRefPubMed
10.
11.
go back to reference Masurel-Paulet A, Poggi-Bach J, Rolland MO, Bernard O, Guffon N, Dobbelaere D, Sarles J, de Baulny HO, Touaty G: NTBC-treatment in tyrosinaemia type I: Long-term outcome in french patients. J Inherit Metab Dis. 2008, 31: 81-87.CrossRefPubMed Masurel-Paulet A, Poggi-Bach J, Rolland MO, Bernard O, Guffon N, Dobbelaere D, Sarles J, de Baulny HO, Touaty G: NTBC-treatment in tyrosinaemia type I: Long-term outcome in french patients. J Inherit Metab Dis. 2008, 31: 81-87.CrossRefPubMed
12.
go back to reference Vondrakova A, Tesarova M, Magner M, Docekalova D, Chrastina P, Prochazkova D, Zeman J, Honzik T: Clinical, biochemical and molecular characteristics in 11 Czech children with tyrosinemia type I. Cas Lek Cesk. 2010, 149: 411-416. Vondrakova A, Tesarova M, Magner M, Docekalova D, Chrastina P, Prochazkova D, Zeman J, Honzik T: Clinical, biochemical and molecular characteristics in 11 Czech children with tyrosinemia type I. Cas Lek Cesk. 2010, 149: 411-416.
13.
go back to reference Couce ML, Dalmau J, del Toro M, Pintos-Morell G, Aldamiz-Echevarria L: Tyrosinemia type I in Spain: Mutational analysis, treatment and long-term outcome. Pediatr Int. 2011, 2011 (53): 985-989.CrossRef Couce ML, Dalmau J, del Toro M, Pintos-Morell G, Aldamiz-Echevarria L: Tyrosinemia type I in Spain: Mutational analysis, treatment and long-term outcome. Pediatr Int. 2011, 2011 (53): 985-989.CrossRef
14.
go back to reference Couce ML, Aldamiz-Echevarria L, Baldellou A, Blasco J, Bueno MA, Dalmau J, De La Vega A, Del Toro M, Diaz C, Lama R, Leao E, Marrero M, Navas VM, Pintos G: Recomendaciones y manejo de la tirosinemia hereditaria Tipo I o Tirosinemia hepatorrenal. An Pediatr (Barc). 2010, 73: 279.e1-279.e4.CrossRef Couce ML, Aldamiz-Echevarria L, Baldellou A, Blasco J, Bueno MA, Dalmau J, De La Vega A, Del Toro M, Diaz C, Lama R, Leao E, Marrero M, Navas VM, Pintos G: Recomendaciones y manejo de la tirosinemia hereditaria Tipo I o Tirosinemia hepatorrenal. An Pediatr (Barc). 2010, 73: 279.e1-279.e4.CrossRef
15.
go back to reference Larochelle J, Alvarez F, Bussières JF, Chevalier I, Dallaire L, Dubois J, Faucher F, Fenyves D, Goodyer P, Grenier A, Holme E, Laframboise R, Lambert M, Lindstedt S, Maranda B, Melancon S, Merouani A, Mitchell J, Parizeault G, Pelletier L, Phan V, Rinaldo P, Scott CR, Scriver C, Mitchell GA: Effect of nitisinone (NTBC) treatment on the clinical course of hepatorenal tyrosinemia in Québec. Mol Genet Metab. 2012, 107: 49-50.CrossRefPubMed Larochelle J, Alvarez F, Bussières JF, Chevalier I, Dallaire L, Dubois J, Faucher F, Fenyves D, Goodyer P, Grenier A, Holme E, Laframboise R, Lambert M, Lindstedt S, Maranda B, Melancon S, Merouani A, Mitchell J, Parizeault G, Pelletier L, Phan V, Rinaldo P, Scott CR, Scriver C, Mitchell GA: Effect of nitisinone (NTBC) treatment on the clinical course of hepatorenal tyrosinemia in Québec. Mol Genet Metab. 2012, 107: 49-50.CrossRefPubMed
16.
go back to reference Schiff M, Broue P, Chabrol B, De Laet C, Habes D, Mention K, Sarles J, Spraul A, Valayannopoulos V, Baulny H: Heterogneity of follow-up procedures in French and Belgian patients with treated hereditary tyrosinemia type I: results of a questionnaire and proposed guidelines. J Inherit Metab Dis. 2011, 35: 823-829.CrossRefPubMed Schiff M, Broue P, Chabrol B, De Laet C, Habes D, Mention K, Sarles J, Spraul A, Valayannopoulos V, Baulny H: Heterogneity of follow-up procedures in French and Belgian patients with treated hereditary tyrosinemia type I: results of a questionnaire and proposed guidelines. J Inherit Metab Dis. 2011, 35: 823-829.CrossRefPubMed
17.
go back to reference Coskun T, Ozalp I, Kocak N, Yüce A, Caglar M, Berger R: Type I hereditary tyrosinaemia: presentation of 11 cases. J Inherit Metab Dis. 1991, 14: 765-770.CrossRefPubMed Coskun T, Ozalp I, Kocak N, Yüce A, Caglar M, Berger R: Type I hereditary tyrosinaemia: presentation of 11 cases. J Inherit Metab Dis. 1991, 14: 765-770.CrossRefPubMed
18.
go back to reference De Laet C, Dionisi-Vici C, Leonard JV, McKiernan P, Mitchell G, Monti L, de Baulny HO, Pintos- Morell G, Spiekerkoetter U: Recommendations for the management of tyrosinaemia type 1. Orphanet J Rare Dis. 2013, 8: 8-CrossRefPubMedPubMedCentral De Laet C, Dionisi-Vici C, Leonard JV, McKiernan P, Mitchell G, Monti L, de Baulny HO, Pintos- Morell G, Spiekerkoetter U: Recommendations for the management of tyrosinaemia type 1. Orphanet J Rare Dis. 2013, 8: 8-CrossRefPubMedPubMedCentral
19.
go back to reference Vockley J, Vockley CM: Clinical trials: curing a critical deficiency in metabolic medicine. Mol Genet Metab. 2010, 99: 244-245.CrossRefPubMed Vockley J, Vockley CM: Clinical trials: curing a critical deficiency in metabolic medicine. Mol Genet Metab. 2010, 99: 244-245.CrossRefPubMed
20.
go back to reference Vockley J, Chapman KA, Arnold GL: Development of clinical guidelines for inborn errors of metabolism: a commentary. Mol Genet Metab. 2013, 108: 203-205.CrossRefPubMed Vockley J, Chapman KA, Arnold GL: Development of clinical guidelines for inborn errors of metabolism: a commentary. Mol Genet Metab. 2013, 108: 203-205.CrossRefPubMed
21.
go back to reference Holme E, Lindstedt S: Tyrosinaemia Type I and NTBC (2-(2-nitro-4-trifluoromethylbenzoyl)-1,3- cyclohexanedione. J Inherit Metab Dis. 1998, 21: 507-517.CrossRefPubMed Holme E, Lindstedt S: Tyrosinaemia Type I and NTBC (2-(2-nitro-4-trifluoromethylbenzoyl)-1,3- cyclohexanedione. J Inherit Metab Dis. 1998, 21: 507-517.CrossRefPubMed
22.
go back to reference Sander J, Janzen N, Peter M, Sander S, Holtkamp U, Schwahn B, Mayatepek E, Trefz FK, Das AM: Newborn Screening or Hepatorenal Tyrosinemia: Tandem Mass Spectrometric Quantification of Succinylacetone. Clin Chem. 2006, 52: 482-487.CrossRefPubMed Sander J, Janzen N, Peter M, Sander S, Holtkamp U, Schwahn B, Mayatepek E, Trefz FK, Das AM: Newborn Screening or Hepatorenal Tyrosinemia: Tandem Mass Spectrometric Quantification of Succinylacetone. Clin Chem. 2006, 52: 482-487.CrossRefPubMed
23.
go back to reference Schulze A, Hoffman GF, Mayatepek E: Spectrophotometric microassay for delta-aminolevulinate dehydratase in dried-blood spots as conformation for hereditary tyrosinemia type I. Clin Chem. 2001, 47: 1424-1429.PubMed Schulze A, Hoffman GF, Mayatepek E: Spectrophotometric microassay for delta-aminolevulinate dehydratase in dried-blood spots as conformation for hereditary tyrosinemia type I. Clin Chem. 2001, 47: 1424-1429.PubMed
24.
go back to reference Zytkovicz TH, Sahai I, Rush A, Odewale A, Johnson D, Fitzgerald E, Britton D, Eaton RB: Newborn screening for hepatorenal tyrosinemia –I by tandem mass spectrometry using pooled samples: A four-year summery by the New England newborn screening program. Clin Biochem. 2013, 46: 681-684.CrossRefPubMed Zytkovicz TH, Sahai I, Rush A, Odewale A, Johnson D, Fitzgerald E, Britton D, Eaton RB: Newborn screening for hepatorenal tyrosinemia –I by tandem mass spectrometry using pooled samples: A four-year summery by the New England newborn screening program. Clin Biochem. 2013, 46: 681-684.CrossRefPubMed
25.
go back to reference Allard P, Grenier A, Korson MS, Zytkovicz TH: Newborn screening for hepatorenal tyrosinemia by tandem mass spectrometry: analysis of succinylacetone extracted from dried blood spots. Clin Biochem. 2004, 37: 1010-1015.CrossRefPubMed Allard P, Grenier A, Korson MS, Zytkovicz TH: Newborn screening for hepatorenal tyrosinemia by tandem mass spectrometry: analysis of succinylacetone extracted from dried blood spots. Clin Biochem. 2004, 37: 1010-1015.CrossRefPubMed
26.
go back to reference Jakob C, Dorland L, Wikkering B, Kok RM, de Jong APJM, Wadman SK: Stable isotope dilution analysis of succinylacetone using eletrone capture negative ion mass fragmentography: an accurate approach to the pre-neonatal diagnosis of hereditary tyrosinemia type I. Clin Chim Acta. 1988, 171: 223-232.CrossRef Jakob C, Dorland L, Wikkering B, Kok RM, de Jong APJM, Wadman SK: Stable isotope dilution analysis of succinylacetone using eletrone capture negative ion mass fragmentography: an accurate approach to the pre-neonatal diagnosis of hereditary tyrosinemia type I. Clin Chim Acta. 1988, 171: 223-232.CrossRef
27.
go back to reference Kvittingen EA, Holme E: Disorders of tyrosine metabolism. Inborn Metabolic Diseases. 3rd edition. Edited by: Fernandes J, Saudubray J-M, Berghe G. 2000, Springer, Heidelberg, 186-194. 3CrossRef Kvittingen EA, Holme E: Disorders of tyrosine metabolism. Inborn Metabolic Diseases. 3rd edition. Edited by: Fernandes J, Saudubray J-M, Berghe G. 2000, Springer, Heidelberg, 186-194. 3CrossRef
28.
go back to reference Magera MJ, Gunawardena ND, Hahn SH, Tortorelli S, Mitchell G, Goodman SI, Rinaldo P, Matern D: Quantative determination of succinylacetone in dried blood spots for newborn screening of tyrosinemia type I. Mol Genet Metab. 2006, 88: 16-21.CrossRefPubMed Magera MJ, Gunawardena ND, Hahn SH, Tortorelli S, Mitchell G, Goodman SI, Rinaldo P, Matern D: Quantative determination of succinylacetone in dried blood spots for newborn screening of tyrosinemia type I. Mol Genet Metab. 2006, 88: 16-21.CrossRefPubMed
29.
go back to reference Mak CM, Lam CW, Chim S, Siu TS, Ng KF, Tam S: Biochemical and molecular diagnosis of tyrosinemia type I with two novel FAH mutations in a Honk Kong Chinese patient: recommendation for expanded newborn screening in Honk Kong. Clin Biochem. 2013, 46: 155-159.CrossRefPubMed Mak CM, Lam CW, Chim S, Siu TS, Ng KF, Tam S: Biochemical and molecular diagnosis of tyrosinemia type I with two novel FAH mutations in a Honk Kong Chinese patient: recommendation for expanded newborn screening in Honk Kong. Clin Biochem. 2013, 46: 155-159.CrossRefPubMed
30.
go back to reference Wu JT, Book L, Sudar K: Serum alpha fetoprotein (AFP) Levels in Normal Infants. Pediatr Res. 1981, 15: 50-52.CrossRefPubMed Wu JT, Book L, Sudar K: Serum alpha fetoprotein (AFP) Levels in Normal Infants. Pediatr Res. 1981, 15: 50-52.CrossRefPubMed
31.
go back to reference Lee PI, Chang MH, Chen DS, Lee CY: Serum α-fetoprotein levels in normal infants: a reappraisal of regression analysis and sex difference. J Pediatr Gastroenterol Nutr. 1989, 8: 19-25.CrossRefPubMed Lee PI, Chang MH, Chen DS, Lee CY: Serum α-fetoprotein levels in normal infants: a reappraisal of regression analysis and sex difference. J Pediatr Gastroenterol Nutr. 1989, 8: 19-25.CrossRefPubMed
32.
go back to reference Bergman AJIW, van den Berg IET, Brink W, Poll-The BT, van Amstel P, Berger R: Spectrum of Mutations in the Fumarylacetoacetate Hydrolase Gene of Tyrosinemia Type I Patients in Northwestern Europe and Mediterranean Countries. Hum Mutat. 1998, 12: 19-26.CrossRefPubMed Bergman AJIW, van den Berg IET, Brink W, Poll-The BT, van Amstel P, Berger R: Spectrum of Mutations in the Fumarylacetoacetate Hydrolase Gene of Tyrosinemia Type I Patients in Northwestern Europe and Mediterranean Countries. Hum Mutat. 1998, 12: 19-26.CrossRefPubMed
33.
go back to reference Halvorsen S: Tyrosinemia. Inborn Metabolic diseases. 1st edition. Edited by: Fernandes J, Saudubray J-M, Tada K. 1990, Springer, Berlin, 199-209.CrossRef Halvorsen S: Tyrosinemia. Inborn Metabolic diseases. 1st edition. Edited by: Fernandes J, Saudubray J-M, Tada K. 1990, Springer, Berlin, 199-209.CrossRef
34.
go back to reference Van Spronsen FJ, Thomasse Y, Smit GPA, Leonard JV, Clayton PT, Fidler V, Berger R, Heymans HAS: Hereditary Tyrosinemia Type I: A New Clinical Classification with Difference in Prognosis on Dietary Treatment. Hepatology. 1994, 20: 1187-1191.CrossRefPubMed Van Spronsen FJ, Thomasse Y, Smit GPA, Leonard JV, Clayton PT, Fidler V, Berger R, Heymans HAS: Hereditary Tyrosinemia Type I: A New Clinical Classification with Difference in Prognosis on Dietary Treatment. Hepatology. 1994, 20: 1187-1191.CrossRefPubMed
35.
go back to reference Dursun A, Ozgül RK, Sivri S, Tokatli A, Güzel A, Mesci L, Kilic M, Alifendiolglu D, Ozcay F, Gündüz M, Coskun T: Mutation Spectrum of Fumarylacetoacetase Gene amd Clinical Aspects of Tyrosinemia Type I Disease. JIMD Rep. 2011, 1: 17-21.CrossRefPubMedPubMedCentral Dursun A, Ozgül RK, Sivri S, Tokatli A, Güzel A, Mesci L, Kilic M, Alifendiolglu D, Ozcay F, Gündüz M, Coskun T: Mutation Spectrum of Fumarylacetoacetase Gene amd Clinical Aspects of Tyrosinemia Type I Disease. JIMD Rep. 2011, 1: 17-21.CrossRefPubMedPubMedCentral
36.
go back to reference Kvittingen EA, Rootwelt H, Berger R, Brandtzaeg P: Self-induced correction of the genetic defect of tyrosinemia type I. J Clin Invest. 1994, 94: 1657-1661.CrossRefPubMedPubMedCentral Kvittingen EA, Rootwelt H, Berger R, Brandtzaeg P: Self-induced correction of the genetic defect of tyrosinemia type I. J Clin Invest. 1994, 94: 1657-1661.CrossRefPubMedPubMedCentral
37.
go back to reference Demers SI, Russo P, Lettre F, Tanguay RM: Frequent mutation inversion correlates with clinical severity in a genetic liver disease, hereditary tyrosinemia. Hum Pathol. 2003, 34: 1313-1320.CrossRefPubMed Demers SI, Russo P, Lettre F, Tanguay RM: Frequent mutation inversion correlates with clinical severity in a genetic liver disease, hereditary tyrosinemia. Hum Pathol. 2003, 34: 1313-1320.CrossRefPubMed
38.
go back to reference Wilson MG, Jungner G: Principles and practice of screening for disease. Public Health Pap. 1968, 34: 26-35. Wilson MG, Jungner G: Principles and practice of screening for disease. Public Health Pap. 1968, 34: 26-35.
39.
go back to reference Sander J, Janzen N, Terhardt M, Sander S, Gökcay G, Dermikol M, Ozer I, Peter M, Das AM: Monitoring tyrosinaemia type I: Blood spot test for nitisinone. Clin Chim Acta. 2011, 412: 134-138.CrossRefPubMed Sander J, Janzen N, Terhardt M, Sander S, Gökcay G, Dermikol M, Ozer I, Peter M, Das AM: Monitoring tyrosinaemia type I: Blood spot test for nitisinone. Clin Chim Acta. 2011, 412: 134-138.CrossRefPubMed
40.
go back to reference Orejuela D, Jorquera R, Bergeron A, Finegold MJ, Tanguay RM, et al: Hepatic stress in hereditary tyrosinemia type 1 (HT1) activates the AKT survival pathway in the fahknockout mice model.J Hepatol 2008, 2008(48):308–317.,CrossRef Orejuela D, Jorquera R, Bergeron A, Finegold MJ, Tanguay RM, et al: Hepatic stress in hereditary tyrosinemia type 1 (HT1) activates the AKT survival pathway in the fahknockout mice model.J Hepatol 2008, 2008(48):308–317.,CrossRef
41.
go back to reference Schlump JU, Perot C, Ketteler K, Schiff M, Mayatepek E, Wendel U, Spiekerkoetter U: Severe neurological crisis in a patient with hereditary tyrosinemia type I after interruption of NTBC. J Inherit Metab Dis. 2008, 31 (Suppl 2): 223-225.CrossRef Schlump JU, Perot C, Ketteler K, Schiff M, Mayatepek E, Wendel U, Spiekerkoetter U: Severe neurological crisis in a patient with hereditary tyrosinemia type I after interruption of NTBC. J Inherit Metab Dis. 2008, 31 (Suppl 2): 223-225.CrossRef
42.
go back to reference Schlune A, Thimm E, Herebian D, Spiekerkoetter U: Single dose NTBC-treatment of hereditary tyrosinemia type I. J Inherit Metab Dis. 2012, 35: 831-836.CrossRefPubMed Schlune A, Thimm E, Herebian D, Spiekerkoetter U: Single dose NTBC-treatment of hereditary tyrosinemia type I. J Inherit Metab Dis. 2012, 35: 831-836.CrossRefPubMed
43.
go back to reference Ahmad S, Teckman JH, Lueder GT: Corneal opacities associated with NTBC treatment. Am J Ophthalmol. 2002, 134: 266-268.CrossRefPubMed Ahmad S, Teckman JH, Lueder GT: Corneal opacities associated with NTBC treatment. Am J Ophthalmol. 2002, 134: 266-268.CrossRefPubMed
44.
go back to reference Gissen P, Preece MA, Willshaw HA, McKiernan PJ: Ophthalmic follow-up of patients with tyrosinaemia type I on NTBC. J Inherit Metab Dis. 2003, 26: 13-16.CrossRefPubMed Gissen P, Preece MA, Willshaw HA, McKiernan PJ: Ophthalmic follow-up of patients with tyrosinaemia type I on NTBC. J Inherit Metab Dis. 2003, 26: 13-16.CrossRefPubMed
45.
go back to reference Holme E: Disorders of tyrosine degradation. Physician’s Guide to the Treatment and Follow-Up of Metabolic Diseases. Edited by: Blau N, Leonard J, Hoffmann GF, Clarke JTR. 2006, Springer, Berlin, 49-56.CrossRef Holme E: Disorders of tyrosine degradation. Physician’s Guide to the Treatment and Follow-Up of Metabolic Diseases. Edited by: Blau N, Leonard J, Hoffmann GF, Clarke JTR. 2006, Springer, Berlin, 49-56.CrossRef
46.
go back to reference Herebian D, Spiekerkoetter U, Lamshöft M, Thimm E, Laryea M, Mayatepek E: Liquid chromatography tandem mass spectrometry method for the quantification of NTBC (2-(2-nitro-4-fluoromethylbenzoyl)-1,3-cyclohexanedione) in plasma of tyrosinemia type I patients. J Chromatogr B. 2009, 877: 1453-1459.CrossRef Herebian D, Spiekerkoetter U, Lamshöft M, Thimm E, Laryea M, Mayatepek E: Liquid chromatography tandem mass spectrometry method for the quantification of NTBC (2-(2-nitro-4-fluoromethylbenzoyl)-1,3-cyclohexanedione) in plasma of tyrosinemia type I patients. J Chromatogr B. 2009, 877: 1453-1459.CrossRef
47.
go back to reference Prieto JA, Andrade F, Lage S, Aldamiz-Echevarria L: Comparison of plasma and dry blood spots as samples for the determination of nitisinone (NTBC) by high-performance liquid chromatography-tandem mass spectrometry. Study of the stability of the samples at different temperatures. J Chromatogr B Analyt Technol Biomed Life Sci. 2011, 879: 671-676.CrossRefPubMed Prieto JA, Andrade F, Lage S, Aldamiz-Echevarria L: Comparison of plasma and dry blood spots as samples for the determination of nitisinone (NTBC) by high-performance liquid chromatography-tandem mass spectrometry. Study of the stability of the samples at different temperatures. J Chromatogr B Analyt Technol Biomed Life Sci. 2011, 879: 671-676.CrossRefPubMed
48.
go back to reference la Marca G, Malvagia S, Materazzi S, Della Bona ML, Boenzi S, Martinelli D, Dionisi- Vici C: LC-MS/MS for simultaneous determination on a dried blood spots of multiple anaytes relevant for treatment monitoring of patients with tyrosinemia type I. Anal Chem. 2012, 84: 1184-1188.CrossRefPubMed la Marca G, Malvagia S, Materazzi S, Della Bona ML, Boenzi S, Martinelli D, Dionisi- Vici C: LC-MS/MS for simultaneous determination on a dried blood spots of multiple anaytes relevant for treatment monitoring of patients with tyrosinemia type I. Anal Chem. 2012, 84: 1184-1188.CrossRefPubMed
49.
go back to reference Daly A, Gokmen–Ozel H, MacDonald A, Preece MA, Davies P, Chakrapani A, McKiernan P: Diurnal variation of phenylalanine concentrations in tyrosinaemia type 1: should we be concerned?. J Hum Nutr Diet. 2012, 25: 111-116.CrossRefPubMed Daly A, Gokmen–Ozel H, MacDonald A, Preece MA, Davies P, Chakrapani A, McKiernan P: Diurnal variation of phenylalanine concentrations in tyrosinaemia type 1: should we be concerned?. J Hum Nutr Diet. 2012, 25: 111-116.CrossRefPubMed
50.
go back to reference Hall MG, Wilks MF, Provan WM, Eksborg S, Lumholtz B: Pharmacokinetics and pharmacodynamics of NTBC (2-(2-nitro-4 fluoromethylbenzpyl)-1,3-cyclohexanedione) and mestrione, inhibitors of 4 hydroxyphenyl pyruvate dioxigenase (HPPD) following a single dose to healthy male volunteers. Br J Clin Pharmocol. 2001, 52: 169-177.CrossRef Hall MG, Wilks MF, Provan WM, Eksborg S, Lumholtz B: Pharmacokinetics and pharmacodynamics of NTBC (2-(2-nitro-4 fluoromethylbenzpyl)-1,3-cyclohexanedione) and mestrione, inhibitors of 4 hydroxyphenyl pyruvate dioxigenase (HPPD) following a single dose to healthy male volunteers. Br J Clin Pharmocol. 2001, 52: 169-177.CrossRef
51.
go back to reference Mohan N, McKiernan P, Preece MA, Green A, Buckels J, Mayer AD, Kelly DA: Indication and outcome of liver tranplantation in tyrosinaemia type 1. Eur J Pediatr. 1999, 158 (Suppl 2): 49-54.CrossRef Mohan N, McKiernan P, Preece MA, Green A, Buckels J, Mayer AD, Kelly DA: Indication and outcome of liver tranplantation in tyrosinaemia type 1. Eur J Pediatr. 1999, 158 (Suppl 2): 49-54.CrossRef
52.
go back to reference Bartlett DC, Preece MA, Holme E, Lloyd C, Newsome PN, McKiernan PJ: Plasma succninylacetone is persistently raised after liver transplantation. J Inherit Metab Dis. 2013, 36: 15-20.CrossRefPubMed Bartlett DC, Preece MA, Holme E, Lloyd C, Newsome PN, McKiernan PJ: Plasma succninylacetone is persistently raised after liver transplantation. J Inherit Metab Dis. 2013, 36: 15-20.CrossRefPubMed
53.
go back to reference Pierik LJWM, van Spronsen FJ, Bijleveld CM, van Dael CM: Renal function in tyrosinaemia type I after liver transplantation: A long-term follow-up. J Inherit Metab Dis. 2005, 28: 871-876.CrossRefPubMed Pierik LJWM, van Spronsen FJ, Bijleveld CM, van Dael CM: Renal function in tyrosinaemia type I after liver transplantation: A long-term follow-up. J Inherit Metab Dis. 2005, 28: 871-876.CrossRefPubMed
54.
go back to reference Santra S, Preece MA, Hulton S-A, McKiernan PJ: Renal tubular function in children with tyrosinaemia type I with nitisinone. J Inherit Metab Dis. 2008, 31: 399-402.CrossRefPubMed Santra S, Preece MA, Hulton S-A, McKiernan PJ: Renal tubular function in children with tyrosinaemia type I with nitisinone. J Inherit Metab Dis. 2008, 31: 399-402.CrossRefPubMed
55.
go back to reference Mohamed S, Kambal MA, Al Jurayyan NA, Al-Nemri A, Babiker A, Hasanato R, Al-Jarallah AS: Tyrosinemia type 1: a rare and forgotten cause of reversible hypertrophic cardiomyopathy in infancy. BMC Res Notes. 2013, 6: 362-CrossRefPubMedPubMedCentral Mohamed S, Kambal MA, Al Jurayyan NA, Al-Nemri A, Babiker A, Hasanato R, Al-Jarallah AS: Tyrosinemia type 1: a rare and forgotten cause of reversible hypertrophic cardiomyopathy in infancy. BMC Res Notes. 2013, 6: 362-CrossRefPubMedPubMedCentral
56.
go back to reference André N, Roquelaure B, Jubin V, Ovaert C: Successful treatment of severe cardiomyopathy with NTBC in a child with tyrosinaemia type I. J Inherit Metab Dis. 2005, 28: 103-106.CrossRefPubMed André N, Roquelaure B, Jubin V, Ovaert C: Successful treatment of severe cardiomyopathy with NTBC in a child with tyrosinaemia type I. J Inherit Metab Dis. 2005, 28: 103-106.CrossRefPubMed
57.
go back to reference Arora N, Stumper O, Wright J, Kelly DA, McKiernan PJ, et al: Cardiomyopathy in tyrosinaemia type I is common but usually benign.J Inherit Metab Dis 2006, 29:54–57.,CrossRefPubMed Arora N, Stumper O, Wright J, Kelly DA, McKiernan PJ, et al: Cardiomyopathy in tyrosinaemia type I is common but usually benign.J Inherit Metab Dis 2006, 29:54–57.,CrossRefPubMed
58.
go back to reference Koelink CJL, Van Hasselt P, der Ploeg V, Van den Heuvel-Eibrink MM, Wijburg FA, Bijlefeld CM, Van Spronsen FJ: Tyrosinemia Typ I treated by NTBC: How does AFP predict liver cancer?. Mol Genet Metab. 2006, 89: 310-315.CrossRefPubMed Koelink CJL, Van Hasselt P, der Ploeg V, Van den Heuvel-Eibrink MM, Wijburg FA, Bijlefeld CM, Van Spronsen FJ: Tyrosinemia Typ I treated by NTBC: How does AFP predict liver cancer?. Mol Genet Metab. 2006, 89: 310-315.CrossRefPubMed
Metadata
Title
Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice
Authors
Sebene Mayorandan
Uta Meyer
Gülden Gokcay
Nuria Garcia Segarra
Hélène Ogier de Baulny
Francjan van Spronsen
Jiri Zeman
Corinne de Laet
Ute Spiekerkoetter
Eva Thimm
Arianna Maiorana
Carlo Dionisi-Vici
Dorothea Moeslinger
Michaela Brunner-Krainz
Amelie Sophia Lotz-Havla
José Angel Cocho de Juan
Maria Luz Couce Pico
René Santer
Sabine Scholl-Bürgi
Hanna Mandel
Yngve Thomas Bliksrud
Peter Freisinger
Luis Jose Aldamiz-Echevarria
Michel Hochuli
Matthias Gautschi
Jessica Endig
Jens Jordan
Patrick McKiernan
Stefanie Ernst
Susanne Morlot
Arndt Vogel
Johannes Sander
Anibh Martin Das
Publication date
01-12-2014
Publisher
BioMed Central
Published in
Orphanet Journal of Rare Diseases / Issue 1/2014
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/s13023-014-0107-7

Other articles of this Issue 1/2014

Orphanet Journal of Rare Diseases 1/2014 Go to the issue