Distribution of ITPA P32T alleles in multiple world populations View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2004-10

AUTHORS

Sharon Marsh, Cristi R. King, Ranjeet Ahluwalia, Howard L. McLeod

ABSTRACT

Dose-limiting toxicity from azathioprine treatment affects up to 37% of patients. Screening for thiopurine methyltransferase (TPMT) polymorphisms will prospectively identify approximately 10% of patients. Recently, a polymorphism in the inosine triphosphate pyrophosphatase gene (ITPA) has been associated with severe azathioprine toxicity. We demonstrate here that this proline to threonine substitution at codon 32 in the ITPA gene is found at low frequency in Central/South American populations (1-2%), at a constant frequency across Caucasian and African populations (6-7%), and is highest in Asian populations (14-19%). This data is consistent with previously described allele frequencies in other Caucasian (7%), African (5%), and Asian (11-15%) populations. This data provides a foundation on which prospective screening studies can be planned to identify patients at risk for severe toxicity from azathioprine therapy. More... »

PAGES

579

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10038-004-0183-y

DOI

http://dx.doi.org/10.1007/s10038-004-0183-y

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PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/15322947


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