Thiopurine methyltransferase (TPMT) and Nudix hydrolase 15 (NUDT15) are key enzymes that catabolize thiopurines. Decreased or no‐function alleles in TPMT and NUDT15 are associated with reduced or no enzyme activity and predictive of pronounced adverse effects, including severe myelosuppression, that may occur among individuals treated with standard doses of thiopurines. Genetic variants in these genes are present in all world populations; however, their frequency varies by ancestry. In this updated guideline, we provide recommendations for adjusting starting doses of mercaptopurine, thioguanine, and azathioprine based on TPMT and NUDT15 genotypes, including for individuals with variants in both genes (updates on www.clinpgx.org ).
Building similarity graph...
Analyzing shared references across papers
Loading...
M. Maillard
St. Jude Children's Research Hospital
Matthias Schwab
Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology
Michelle Whirl-Carrillo
Palo Alto University
Clinical Pharmacology & Therapeutics
Stanford University
The University of Tokyo
Mayo Clinic
Building similarity graph...
Analyzing shared references across papers
Loading...
Maillard et al. (Sat,) studied this question.
synapsesocial.com/papers/6980fefbc1c9540dea811919 — DOI: https://doi.org/10.1002/cpt.70209