HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Recipient/donor contradictory genotypes with impact on drug pharmacogenetics after liver transplant: a deadly gift?

Abstract
A 5-year-old girl who had undergone liver transplantation was scheduled for treatment with high-dose cytarabine for a Burkitt lymphoma. Because of impaired transplantation, a study of cytidine deaminase (CDA), the liver enzyme responsible for cytarabine detoxification, was conducted before initiating treatment to evaluate the risk for toxicity in this patient. The CDA genotype and phenotype were both studied and showed none of the polymorphisms usually associated with impaired CDA, but surprisingly functional deficiency was observed. Despite a subsequent 30% reduction in cytarabine dosing, life-threatening toxicities appeared quickly and treatment was discontinued. Further genetic investigations performed on liver biopsy showed that the donor was actually homozygous for CDA*2, a genotype associated with severe CDA deficiency. On the basis of the liver genotype, treatment was resumed with further dose reduction, which led to a better tolerance. This case report highlights the limits of searching germline polymorphisms in patients with liver transplant when the story plays in the liver.
AuthorsCindy Serdjebi, Joseph Ciccolini, Frederic Fina, Arnauld Delarue, Arnauld Verschuur, Bruno Lacarelle, L'Houcine Ouafik, Nicolas André
JournalPharmacogenetics and genomics (Pharmacogenet Genomics) Vol. 24 Issue 10 Pg. 527-9 (Oct 2014) ISSN: 1744-6880 [Electronic] United States
PMID25003625 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antimetabolites, Antineoplastic
  • Cytarabine
  • Cytidine Deaminase
Topics
  • Antimetabolites, Antineoplastic (administration & dosage, adverse effects)
  • Burkitt Lymphoma (drug therapy, genetics)
  • Child, Preschool
  • Cytarabine (administration & dosage, adverse effects)
  • Cytidine Deaminase (deficiency, genetics)
  • Dose-Response Relationship, Drug
  • Female
  • Germ-Line Mutation
  • Humans
  • Liver Transplantation (adverse effects)
  • Polymorphism, Genetic

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: