Literature DB >> 34628487

Evaluation of dynamic thiol/disulfide homeostasis in hereditary tyrosinemia type 1 patients.

Ayse Cigdem Aktuglu Zeybek1, Ertugrul Kiykim2, Salim Neselioglu3, Halise Zeynep Iscan4, Tanyel Zubarioglu2, Mehmet Serif Cansever5, Ozcan Erel3.   

Abstract

BACKGROUND: Despite successful treatment with nitisinone, the pathophysiology of long-term complications, including hepatocellular carcinoma and mental decline in tyrosinemia type 1 patients, is still obscure. Oxidative stress may play a role in these complications. While increased fumarylacetoacetate and maleylacetoacetate cause oxidative stress in the liver, increased tyrosine causes oxidative stress in the brain. The aim of this study is to evaluate dynamic thiol/disulfide homeostasis as an indicator of oxidative stress in late-diagnosed tyrosinemia type 1 patients.
METHODS: Twenty-four late-diagnosed (age of diagnosis; 14.43 ± 26.35 months) tyrosinemia type 1 patients (19 under nitisinone treatment and 5 with liver transplantation) and 25 healthy subjects were enrolled in the study. Serum native thiol, total thiol, and disulfide levels were measured, and disulfide/native, disulfide/total, and native thiol/total thiol ratios were calculated from these values.
RESULTS: No significant difference was observed in native, total, and disulfide thiol levels between the groups and no increase in disulfide/native, disulfide/total, and native/total thiol ratios was detected, despite significantly higher plasma tyrosine levels in the nitisinone-treated group.
CONCLUSIONS: We suggest that providing sufficient metabolic control with good compliance to nitisinone treatment can help to prevent oxidative stress in late-diagnosed tyrosinemia type 1 patients. IMPACT: Despite successful nitisinone (NTBC) treatment, the underlying mechanisms of long-term complications in hereditary tyrosinemia type 1 (HT1), including hepatocellular carcinoma and mental decline, are still obscure. Oxidative stress may play a role in these complications. Thiol/disulfide homeostasis, which is an indicator of oxidative stress, is not disturbed in hereditary tyrosinemia patients under NTBC treatment, despite higher plasma tyrosine levels and patients who had liver transplantation. This is the first study evaluating dynamic thiol/disulfide homeostasis as an indicator of oxidative stress in late-diagnosed HT1 patients.
© 2021. The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc.

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Year:  2021        PMID: 34628487     DOI: 10.1038/s41390-021-01770-6

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.953


  44 in total

1.  HCC prevalence and histopathological findings in liver explants of patients with hereditary tyrosinemia type 1.

Authors:  Joao Seda Neto; Katia M R Leite; Adriana Porta; Eduardo A Fonseca; Flavia H Feier; Renata Pugliese; Irene K Miura; Paulo Chapchap; Gilda Porta
Journal:  Pediatr Blood Cancer       Date:  2014-05-22       Impact factor: 3.167

2.  Outcome of children with hereditary tyrosinaemia following newborn screening.

Authors:  P J McKiernan; Mary Anne Preece; Anupam Chakrapani
Journal:  Arch Dis Child       Date:  2015-01-06       Impact factor: 3.791

Review 3.  Nontransplant treatment of tyrosinemia.

Authors:  E Holme; S Lindstedt
Journal:  Clin Liver Dis       Date:  2000-11       Impact factor: 6.126

Review 4.  Molecular Aspects of the FAH Mutations Involved in HT1 Disease.

Authors:  Geneviève Morrow; Francesca Angileri; Robert M Tanguay
Journal:  Adv Exp Med Biol       Date:  2017       Impact factor: 2.622

5.  Hereditary tyrosinemia type I: a new clinical classification with difference in prognosis on dietary treatment.

Authors:  F J van Spronsen; Y Thomasse; G P Smit; J V Leonard; P T Clayton; V Fidler; R Berger; H S Heymans
Journal:  Hepatology       Date:  1994-11       Impact factor: 17.425

6.  Cardiomyopathy in tyrosinaemia type I is common but usually benign.

Authors:  N Arora; O Stumper; J Wright; D A Kelly; P J McKiernan
Journal:  J Inherit Metab Dis       Date:  2006-02       Impact factor: 4.982

7.  Hyperinsulinism in tyrosinaemia type I.

Authors:  U Baumann; M A Preece; A Green; D A Kelly; P J McKiernan
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.982

8.  Early nitisinone treatment reduces the need for liver transplantation in children with tyrosinaemia type 1 and improves post-transplant renal function.

Authors:  David C Bartlett; Carla Lloyd; Patrick J McKiernan; Phil N Newsome
Journal:  J Inherit Metab Dis       Date:  2014-02-11       Impact factor: 4.982

9.  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
Journal:  Orphanet J Rare Dis       Date:  2014-08-01       Impact factor: 4.123

Review 10.  Long-Term Outcomes and Practical Considerations in the Pharmacological Management of Tyrosinemia Type 1.

Authors:  Willem G van Ginkel; Iris L Rodenburg; Cary O Harding; Carla E M Hollak; M Rebecca Heiner-Fokkema; Francjan J van Spronsen
Journal:  Paediatr Drugs       Date:  2019-12       Impact factor: 3.022

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