| Literature DB >> 18250137 |
U Boonsrirat1, S Angsuthum, S Vannaprasaht, J Kongpunvijit, N Hirankarn, W Tassaneeyakul, Y Avihingsanon.
Abstract
Azathioprine (AZA) is a commonly used immunosuppressant for systemic lupus erythematosus (SLE). Myelosuppression is a serious adverse reaction due to AZA and its metabolites. Thiopurine S-methyltransferase (TPMT) is the rate-limiting enzyme. Variations of TPMT enzyme activity may be responsible for myelosuppression. However, a correlation between certain mutant alleles of low TPMT enzyme activity and myelotoxicity has also been suggested as a factor. We describe herein a case of AZA-induced severe myelosuppression associated with TPMT*3C heterozygous mutant allele in a SLE patient. The patient presented with pancytopenia, sepsis, typhlitis and disseminated intravascular coagulopathy after a short period of AZA therapy. The patient had low TPMT activity and TPMT*3C genotype. Measurement of TPMT activity and determination of TPMT variant allele may identify patients at risk for AZA-induced myelosuppression.Entities:
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Year: 2008 PMID: 18250137 DOI: 10.1177/0961203307085255
Source DB: PubMed Journal: Lupus ISSN: 0961-2033 Impact factor: 2.911