Abstract | BACKGROUND: AIM: To evaluate the results of initial AZA/MP metabolite panels sent by gastroenterologists during the first year of its widespread availability. METHODS: Initial AZA/MP metabolite panels sent by gastroenterologists to a single laboratory were reviewed and the metabolite panels were interpreted. RESULTS: Initial metabolite levels were reviewed for 9187 patients. Noncompliance was detected in 263 patients (3%) and under-dosing in 4260 patients (46%). 534 patients (6%) had levels that were consistent with preferential metabolism via the TPMT pathway. The therapeutic goal was achieved in 2444 patients (27%) and an additional 552 patients (6%) had appropriate TG levels but potential hepatotoxicity. 936 patients (10%) had potential TPMT deficiency, and 58 patients (1%) had potential TPMT absence and were at risk for leukopenia. 140 patients (2%) had too high a dose. CONCLUSIONS: Measurement of AZA/MP metabolites can be used by practising gastroenterologists to identify potential reasons for nonresponse to AZA or MP, and to identify patients at risk for certain drug-related toxicities.
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Authors | R S Bloomfeld, J E Onken |
Journal | Alimentary pharmacology & therapeutics
(Aliment Pharmacol Ther)
Vol. 17
Issue 1
Pg. 69-73
(Jan 2003)
ISSN: 0269-2813 [Print] England |
PMID | 12492734
(Publication Type: Journal Article)
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Chemical References |
- 6-methylthiopurine
- Mercaptopurine
- Thioguanine
- Azathioprine
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Topics |
- Azathioprine
(metabolism)
- Humans
- Inflammatory Bowel Diseases
(drug therapy, metabolism)
- Mercaptopurine
(analogs & derivatives, metabolism, therapeutic use)
- Patient Compliance
- Risk Factors
- Thioguanine
(metabolism)
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