Literature DB >> 33679043

Outcome of Tyrosinemia Type 1 in Indian Children.

Sonal Mirani1, Vishrutha Poojari1, Naman S Shetty1, Ira Shah1,2.   

Abstract

AIM: The objective of this study was to determine the outcome of children with tyrosinemia type 1 from India.
METHODS: A retrospective observational study was conducted on 11 patients diagnosed with type I tyrosinemia under our care. Age at symptoms, age at diagnosis, age at starting 2-nitro-4-trifluoromethylbenzoyl-1,3-cyclohexanedione (NTBC), duration between diagnosis and initiation of NTBC, dose given, total duration of NTBC, and outcomes were noted.
RESULTS: Eleven children with a median age of 1.1 years (0.51-1.52) at onset of symptoms were included in the study. The median age at diagnosis was 1.76 years (0.95-2.43). Their current median age is 5.44 (2.36-8.80) years. Common clinical features at presentation were chronic liver disease in 8 (72.72%), rickets in 2 (18.18%), and fulminant liver disease in 1 (9.09%) patient. Hepatomegaly was observed in all children, growth retardation in 9 (81.81%), coagulopathy in 8 (72.72%), and abdominal distention in 6 (54.54%) patients. The median duration of NTBC therapy was 13.5 (7-21.25) months. The median dose of NTBC was 1 (0.77-1) mg/kg/day. One (9.09%) patient died due to liver cell failure. However, she had received NTBC only for a month. Another patient developed hepatocellular carcinoma (HCC) and underwent liver transplantation. He could receive NTBC only for 2 months, although he was diagnosed to have tyrosinemia for over a 1 year. Eight patients are on treatment with NTBC and are doing well, and 1 patient is not on NTBC and continues to have renal tubular acidosis.
CONCLUSION: NTBC therapy is effective and improves the prognosis of tyrosinemia. A long-term follow-up is required to determine progression to HCC and need for liver transplantation.
© 2020 Indian National Association for Study of the Liver. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  AFP, Alpha-feto Protein; ALP, Alkaline Phosphatase; CLD, Chronic Liver Disease; GGPT, γ-glutamine Transaminase; HCC, Hepatocellular Carcinoma; INR, International Normalized Ratio; LFT, Liver Function Test; NTBC; NTBC, 2-nitro-4-trifluoromethylbenzoyl-1,3-cyclohexanedione; RTA, Renal Tubular Acidosis; SA, Succinylacetone; SGOT, Aspartate Transaminase; SGPT, Alanine Transaminase; Tyrosinemia type 1; hepatocellular carcinoma; liver transplant; succinylacetone

Year:  2020        PMID: 33679043      PMCID: PMC7897851          DOI: 10.1016/j.jceh.2020.07.002

Source DB:  PubMed          Journal:  J Clin Exp Hepatol        ISSN: 0973-6883


  10 in total

1.  Hereditary tyrosinemia type 1 from a single center in Egypt: clinical study of 22 cases.

Authors:  Hanaa El-Karaksy; Mona Fahmy; Mona El-Raziky; Nehal El-Koofy; Rokaya El-Sayed; Mohamed S Rashed; Hasan El-Kiki; Ahmad El-Hennawy; Nabil Mohsen
Journal:  World J Pediatr       Date:  2011-06-01       Impact factor: 2.764

2.  Hepatocellular carcinoma in hereditary tyrosinemia type I despite 2-(2 nitro-4-3 trifluoro- methylbenzoyl)-1, 3-cyclohexanedione treatment.

Authors:  Francjan J van Spronsen; Charles M A Bijleveld; Bianca T van Maldegem; Frits A Wijburg
Journal:  J Pediatr Gastroenterol Nutr       Date:  2005-01       Impact factor: 2.839

3.  Tyrosinemia type 1 in Spain: mutational analysis, treatment and long-term outcome.

Authors:  Maria Luz Couce; Jaime Dalmau; Mireia del Toro; Guillem Pintos-Morell; Luís Aldámiz-Echevarría
Journal:  Pediatr Int       Date:  2011-12       Impact factor: 1.524

Review 4.  Nontransplant treatment of tyrosinemia.

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

5.  Geographical and Ethnic Distribution of Mutations of the Fumarylacetoacetate Hydrolase Gene in Hereditary Tyrosinemia Type 1.

Authors:  Francesca Angileri; Anne Bergeron; Geneviève Morrow; Francine Lettre; George Gray; Tim Hutchin; Sarah Ball; Robert M Tanguay
Journal:  JIMD Rep       Date:  2015-02-15

6.  Nitisinone in the treatment of hereditary tyrosinaemia type 1.

Authors:  Patrick J McKiernan
Journal:  Drugs       Date:  2006       Impact factor: 9.546

7.  NTBC treatment in tyrosinaemia type I: long-term outcome in French patients.

Authors:  A Masurel-Paulet; J Poggi-Bach; M-O Rolland; O Bernard; N Guffon; D Dobbelaere; J Sarles; H Ogier de Baulny; G Touati
Journal:  J Inherit Metab Dis       Date:  2008-01-25       Impact factor: 4.982

Review 8.  Experience of nitisinone for the pharmacological treatment of hereditary tyrosinaemia type 1.

Authors:  Saikat Santra; Ulrich Baumann
Journal:  Expert Opin Pharmacother       Date:  2008-05       Impact factor: 3.889

9.  The outcome of seven patients with hereditary tyrosinemia type 1.

Authors:  Songul Gokay; Pembe Soylu Ustkoyuncu; Fatih Kardas; Mustafa Kendirci
Journal:  J Pediatr Endocrinol Metab       Date:  2016-10-01       Impact factor: 1.634

10.  Hereditary tyrosinemia type 1 in Turkey: twenty year single-center experience.

Authors:  A Cigdem Aktuglu Zeybek; Ertugrul Kiykim; Erdogan Soyucen; Serif Cansever; Suheyla Altay; Tanyel Zubarioglu; Tulay Erkan; Ahmet Aydin
Journal:  Pediatr Int       Date:  2014-12-11       Impact factor: 1.524

  10 in total

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