Literature DB >> 24485820

Significant hepatic involvement in patients with ornithine transcarbamylase deficiency.

Renata C Gallagher1, Christina Lam2, Derek Wong2, Stephen Cederbaum2,3, Ronald J Sokol4.   

Abstract

OBJECTIVE: To determine the frequency of significant liver injury and acute liver failure (ALF) in patients with ornithine transcarbamylase deficiency (OTCD), the most common urea cycle defect. STUDY
DESIGN: In this historical cohort study, charts of 71 patients with OTCD at 2 centers were reviewed to assess the prevalence of ALF (international normalized ratio [INR] ≥2.0), liver dysfunction (INR 1.5-1.99), and hepatocellular injury (aspartate aminotransferase/alanine aminotransferase ≥250 IU/L).
RESULTS: More than one-half (57%) of the 49 patients with symptomatic OTCD had liver involvement; 29% met the criteria for ALF, 20% had liver dysfunction, and 8% had isolated hepatocellular injury. The prevalence of ALF was highest in the patients with more severe OTCD, including those with markedly elevated ammonia levels (>1000 μmol/L). Some patients with severe liver involvement (INR ≥2.0 and aspartate aminotransferase/alanine aminotransferase >1000 IU/L) had only moderate hyperammonemia (ammonia 100-400 μmol/L). ALF was the initial presenting symptom of OTCD in at least 3 of 49 symptomatic patients with OTCD.
CONCLUSION: Episodes of hepatocellular injury, liver dysfunction, and ALF were identified in a high proportion of children with symptomatic OTCD. The more severely affected patients had a higher likelihood of ALF. The diagnosis of a urea cycle defect should be considered in patients with unexplained ALF, liver dysfunction, or hepatocellular injury.
Copyright © 2014 Mosby, Inc. All rights reserved.

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Year:  2014        PMID: 24485820      PMCID: PMC4070427          DOI: 10.1016/j.jpeds.2013.12.024

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  60 in total

1.  Hyperammonaemia due to ornithine transcarbamylase deficiency.

Authors:  I J Hopkins; J F Connelly; A G Dawson; F J Hird; T G Maddison
Journal:  Arch Dis Child       Date:  1969-04       Impact factor: 3.791

2.  Heritable urea cycle enzyme deficiency-liver disease in 16 patients.

Authors:  D R LaBrecque; P S Latham; C A Riely; Y E Hsia; G Klatskin
Journal:  J Pediatr       Date:  1979-04       Impact factor: 4.406

Review 3.  Unmasked adult-onset urea cycle disorders in the critical care setting.

Authors:  Marshall L Summar; Frederick Barr; Sheila Dawling; Wendy Smith; Brendan Lee; Rani H Singh; William J Rhead; Lisa Sniderman King; Brian W Christman
Journal:  Crit Care Clin       Date:  2005-10       Impact factor: 3.598

4.  Adult onset urea cycle disorder in a patient with presumed hepatic encephalopathy.

Authors:  Muslim Atiq; Andrew F Holt; Kamran Safdar; Frederick Weber; Ravi Ravinuthala; Mark E Jonas; Guy W Neff
Journal:  J Clin Gastroenterol       Date:  2008-02       Impact factor: 3.062

5.  High urgency liver transplantation in ornithine transcarbamylase deficiency presenting with acute liver failure.

Authors:  Ulrike Teufel; Jürgen Weitz; Christa Flechtenmacher; Viola Prietsch; Jan Schmidt; Georg F Hoffmann; Stefan Kölker; Guido Engelmann
Journal:  Pediatr Transplant       Date:  2009-04-26

6.  Reye's syndrome due to a novel protein-tolerant variant of ornithine-transcarbamylase deficiency.

Authors:  M M Thaler; N J Hoogenraad; M Boswell
Journal:  Lancet       Date:  1974-08-24       Impact factor: 79.321

7.  Hyperammonemia due to a defect in hepatic ornithine transcarbamylase.

Authors:  P Sunshine; J E Lindenbaum; H L Levy; J M Freeman
Journal:  Pediatrics       Date:  1972-07       Impact factor: 7.124

8.  Progressive liver fibrosis in late-onset argininosuccinate lyase deficiency.

Authors:  Toshihiko Mori; Kazushige Nagai; Michio Mori; Masayoshi Nagao; Masakatsu Imamura; Mikio Iijima; Keiko Kobayashi
Journal:  Pediatr Dev Pathol       Date:  2002-10-10

9.  Liver peroxisome damage during acute hepatic failure in partial ornithine transcarbamylase deficiency.

Authors:  P Landrieu; B François; G Lyon; F Van Hoof
Journal:  Pediatr Res       Date:  1982-12       Impact factor: 3.756

10.  Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency.

Authors:  M L Batshaw; M Msall; A L Beaudet; J Trojak
Journal:  J Pediatr       Date:  1986-02       Impact factor: 4.406

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  20 in total

1.  The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation.

Authors:  Stefan Kölker; Angeles Garcia-Cazorla; Angeles Garcia Cazorla; Vassili Valayannopoulos; Allan M Lund; Alberto B Burlina; Jolanta Sykut-Cegielska; Frits A Wijburg; Elisa Leão Teles; Jiri Zeman; Carlo Dionisi-Vici; Ivo Barić; Daniela Karall; Persephone Augoustides-Savvopoulou; Lise Aksglaede; Jean-Baptiste Arnoux; Paula Avram; Matthias R Baumgartner; Javier Blasco-Alonso; Brigitte Chabrol; Anupam Chakrapani; Kimberly Chapman; Elisenda Cortès I Saladelafont; Maria L Couce; Linda de Meirleir; Dries Dobbelaere; Veronika Dvorakova; Francesca Furlan; Florian Gleich; Wanda Gradowska; Stephanie Grünewald; Anil Jalan; Johannes Häberle; Gisela Haege; Robin Lachmann; Alexander Laemmle; Eveline Langereis; Pascale de Lonlay; Diego Martinelli; Shirou Matsumoto; Chris Mühlhausen; Hélène Ogier de Baulny; Carlos Ortez; Luis Peña-Quintana; Danijela Petković Ramadža; Esmeralda Rodrigues; Sabine Scholl-Bürgi; Etienne Sokal; Christian Staufner; Marshall L Summar; Nicholas Thompson; Roshni Vara; Inmaculada Vives Pinera; John H Walter; Monique Williams; Peter Burgard
Journal:  J Inherit Metab Dis       Date:  2015-04-15       Impact factor: 4.982

2.  Acute liver dysfunction with delayed peak of serum aminotransferase levels as a presentation of ornithine transcarbamylase deficiency in females.

Authors:  Kathryn Clarkston; Joy Lee; Sarah Donoghue; Heidi Peters; Hernan Eiroa; Amit A Shah; Kathleen Loomes; Jessica Wen; Mark Oliver; Winita Hardikar; Carlos E Prada; Akihiro Asai
Journal:  Am J Med Genet A       Date:  2020-12-24       Impact factor: 2.802

3.  Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disorders-A successful strategy for clinical research of rare diseases.

Authors:  Roland Posset; Sven F Garbade; Nikolas Boy; Alberto B Burlina; Carlo Dionisi-Vici; Dries Dobbelaere; Angeles Garcia-Cazorla; Pascale de Lonlay; Elisa Leão Teles; Roshni Vara; Nicholas Ah Mew; Mark L Batshaw; Matthias R Baumgartner; Shawn E McCandless; Jennifer Seminara; Marshall Summar; Georg F Hoffmann; Stefan Kölker; Peter Burgard
Journal:  J Inherit Metab Dis       Date:  2019-01       Impact factor: 4.982

Review 4.  A longitudinal study of urea cycle disorders.

Authors:  Mark L Batshaw; Mendel Tuchman; Marshall Summar; Jennifer Seminara
Journal:  Mol Genet Metab       Date:  2014-08-10       Impact factor: 4.797

Review 5.  Arginase-1 deficiency.

Authors:  Yuan Yan Sin; Garrett Baron; Andreas Schulze; Colin D Funk
Journal:  J Mol Med (Berl)       Date:  2015-10-14       Impact factor: 4.599

6.  Chronic liver disease and impaired hepatic glycogen metabolism in argininosuccinate lyase deficiency.

Authors:  Lindsay C Burrage; Simran Madan; Xiaohui Li; Saima Ali; Mahmoud Mohammad; Bridget M Stroup; Ming-Ming Jiang; Racel Cela; Terry Bertin; Zixue Jin; Jian Dai; Danielle Guffey; Milton Finegold; Sandesh Nagamani; Charles G Minard; Juan Marini; Prakash Masand; Deborah Schady; Benjamin L Shneider; Daniel H Leung; Deeksha Bali; Brendan Lee
Journal:  JCI Insight       Date:  2020-02-27

Review 7.  Genotype-Phenotype Correlations in Ornithine Transcarbamylase Deficiency: A Mutation Update.

Authors:  Ljubica Caldovic; Iman Abdikarim; Sahas Narain; Mendel Tuchman; Hiroki Morizono
Journal:  J Genet Genomics       Date:  2015-05-19       Impact factor: 4.275

Review 8.  Metabolic Liver Disease: When to Suspect and How to Diagnose?

Authors:  Seema Alam; Vikrant Sood
Journal:  Indian J Pediatr       Date:  2016-04-29       Impact factor: 1.967

9.  Hepatocyte selection medium eliminating induced pluripotent stem cells among primary human hepatocytes.

Authors:  Minoru Tomizawa; Fuminobu Shinozaki; Yasufumi Motoyoshi; Takao Sugiyama; Shigenori Yamamoto; Naoki Ishige
Journal:  World J Methodol       Date:  2015-09-26

10.  Liver Failure as the Presentation of Ornithine Transcarbamylase Deficiency in a 13-Month-Old Female.

Authors:  Farrah Rajabi; Lance H Rodan; Maureen M Jonas; Janet S Soul; Nicole J Ullrich; Ann Wessel; Susan E Waisbren; Wen-Hann Tan; Gerard T Berry
Journal:  JIMD Rep       Date:  2017-09-09
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