Lara Colleoni, Dimos Kapetis, Lorenzo Maggi, Giorgia Camera, Eleonora Canioni, Paola Cavalcante, Nicole Kerlero de Rosbo, Fulvio Baggi, Carlo Antozzi, Paolo Confalonieri, Renato Mantegazza, Pia Bernasconi
Neurology IV, Foundation IRCCS Neurological Institute Carlo Besta, Milan, Italy.
Journal of clinical pharmacology 2013 JanThe authors have analyzed single nucleotide polymorphisms in the thiopurine S-methyltransferase (TPMT) gene in the context of efficacy and toxicity of azathioprine (AZA) to determine possible genotype-phenotype correlations between TPMT allelic variants and response to AZA treatment in 76 Italian patients with myasthenia gravis. They confirm known intronic and exonic TPMT polymorphisms that do not correlate with AZA responses and demonstrate a novel intronic polymorphism in a patient intolerant to AZA. Most importantly, they show that of the 22 AZA-intolerant patients, all 5 who carried mutations of the intolerance-linked haplotype TPMT*3A also carried the intronic T140+114A (rs3931660), all 3 mutations being part of a new haplotype designated TMPT*3E. TPMT*3E was not observed in unresponsive or responsive patients. The association of TPMT*3E with AZA intolerance and its frequency must be ascertained in larger, ethnically different cohorts. Nevertheless, in view of the highly significant association (Psim = 0.0026) between TPMT*3E and AZA intolerance in the study, this new haplotype should be taken into consideration in pharmacogenetic profiling for AZA. © 2012 The Author(s).
Lara Colleoni, Dimos Kapetis, Lorenzo Maggi, Giorgia Camera, Eleonora Canioni, Paola Cavalcante, Nicole Kerlero de Rosbo, Fulvio Baggi, Carlo Antozzi, Paolo Confalonieri, Renato Mantegazza, Pia Bernasconi. A new thiopurine s-methyltransferase haplotype associated with intolerance to azathioprine. Journal of clinical pharmacology. 2013 Jan;53(1):67-74
PMID: 23400745
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