AI Article Synopsis

  • Hepatotoxicity is a common issue in children undergoing maintenance therapy for acute lymphoblastic leukemia (ALL) due to medications like 6-mercaptopurine and methotrexate.
  • Elevated levels of methylated 6-mercaptopurine metabolites (MeMP) are linked to increased liver damage, but other mechanisms remain unclear.
  • A study examining POLG gene variants in 34 ALL patients identified four variants in 12 individuals, including one patient with severe liver damage that did not show high MeMP levels, indicating a potential specific genetic link to hepatotoxicity.

Article Abstract

Hepatotoxicity is a frequent complication during maintenance therapy of acute lymphoblastic leukemia (ALL) with 6-mercaptopurine and methotrexate. Elevated levels of methylated 6-mercaptopurine metabolites (MeMP) are associated with hepatotoxicity. However, not all mechanisms are known that lead to liver failure in patients with ALL. Variants in the POLG gene, which encodes the catalytic subunit of mitochondrial DNA polymerase gamma (POLG1), have been related to drug-induced hepatotoxicity, for example, by sodium valproate. The association of common POLG variants with hepatotoxicity during maintenance therapy was studied in 34 patients with childhood ALL. Of the screened POLG variants, four different variants were detected in 12 patients. One patient developed severe hepatotoxicity without elevated MeMP levels and harbored a heterozygous POLG p.G517V variant, which was not found in the other patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506908PMC
http://dx.doi.org/10.1038/s41397-023-00303-0DOI Listing

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