Literature DB >> 17479648

Acetaminophen-induced hepatotoxicity in a glutathione synthetase-deficient patient.

Ayşegül Tokatli1, H Serap Kalkanoğlu-Sivri, Aysel Yüce, Turgay Coşkun.   

Abstract

We report a patient with glutathione synthetase (GS) deficiency who developed acetaminophen-induced hepatotoxicity after a two-day treatment with regular doses of acetaminophen. A nine-month-old female was referred because of intractable metabolic acidosis. She was given acetaminophen at therapeutic doses over a 48-hour period. She was hospitalized because of confusion and metabolic acidosis. Liver function tests were abnormal with normal bilirubin levels. The urine gas chromatography-mass spectrometry (GC/MS) showed massive excretion of 5-oxoproline. She improved and liver function tests normalized in the next six days, but compensated metabolic acidosis and massive 5-oxoprolinuria persisted. The analysis of GS in erythrocytes revealed 5% of normal enzyme activity, and the patient had 491G > A mutation on both alleles in the GS gene. In this report it can be assumed that patients, even if heterozygous for a mutation of the GS gene, are at risk for acetaminophen toxicity.

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Year:  2007        PMID: 17479648

Source DB:  PubMed          Journal:  Turk J Pediatr        ISSN: 0041-4301            Impact factor:   0.552


  2 in total

1.  5-Oxoprolinuria as a cause of high anion gap metabolic acidosis.

Authors:  Rajanshu Verma; Karthik R Polsani; Jeffrey Wilt; Mark E Loehrke
Journal:  Br J Clin Pharmacol       Date:  2012-03       Impact factor: 4.335

2.  Rifampicin-activated human pregnane X receptor and CYP3A4 induction enhance acetaminophen-induced toxicity.

Authors:  Jie Cheng; Xiaochao Ma; Kristopher W Krausz; Jeffrey R Idle; Frank J Gonzalez
Journal:  Drug Metab Dispos       Date:  2009-05-21       Impact factor: 3.922

  2 in total

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