Non-thiopurine methyltransferase related effects in 6-mercaptopurine therapy
View Patent ↗The present invention provides methods for predicting tolerance associated with 6-mercaptopurine drug treatment of an immune-mediated gastrointestinal disorder such as inflammatory bowel disease. In particular, the present invention provides methods for predicting a patient's risk of an adverse drug reaction (or tolerance) to a 6-mercaptopurine drug by genotyping a patient at a polymorphic site in at least one gene selected from the group consisting of a xanthine dehydrogenase (XDH) gene, molybdenum cofactor sulfurase (MOCOS) gene, and aldehyde oxidase (AOX) gene. The present invention further provides methods for optimizing therapeutic efficacy in a patient receiving a 6-mercaptopurine drug by determining whether the patient should be given an alternative drug based on the presence or absence of a polymorphism in at least one of the XDH, MOCOS, and AOX genes.
1. A method for identifying a human subject who is likely to lack response to azathioprine (AZA) or 6-mercaptopurine (6-MP), said method comprising:
(a) genotyping nucleic acid in a sample from said subject for the presence of the 3404 A to G mutation in the Aldehyde oxidase (AOX) coding sequence;
(b) detecting a G at position 3404 in the AOX coding sequence; and
(c) identifying the subject as likely to lack response to AZA or 6-MP when a G at position 3404 in the AOX coding sequence is detected.
2. The method of claim 1 , wherein said individual has a disease or disorder selected from the group consisting of an immune-mediated gastrointestinal disorder, an autoimmune disease, and graft versus host disease.
3. The method of claim 2 , wherein said immune-mediated gastrointestinal disorder is inflammatory bowel disease.
4. The method of claim 1 , wherein the method further comprises genotyping thiopurine methyltransferase (TPMT).
5. A method for treating a human subject having inflammatory bowel disease (IBD), said method comprising:
(a) genotyping nucleic acid in a sample from said subject for the presence of the 3404 A to G mutation in the Aldehyde oxidase (AOX) coding sequence;
(b) detecting a G at position 3404 in the AOX coding sequence; and
(c) treating the human subject having the presence of a G at position 3404 in the AOX coding sequence with a drug other than AZA or 6-MP.
6. The method of claim 5 , wherein said drug other than AZA or 6-MP is an anti-inflammatory agent.
7. The method of claim 6 , wherein said anti-inflammatory agent is infliximab.
8. The method of claim 5 , wherein said drug other than AZA or 6-MP is an immunosuppressive agent.
9. The method of claim 5 , wherein the human subject having IBD has Crohn's disease.
10. The method of claim 1 or 5 , wherein the method further comprises genotyping the xanthine dehydrogenase (XDH) gene for a variant allele selected from the group consisting of 2211C>T (exon 21), 3030T>C (exon 27), 837 C>T (exon 10), 37170>A (exon 34), 2107A>G (exon 20), 1936 A>G (exon 18) and a combination thereof.
11. The method of claim 1 or 5 , wherein the method further comprises genotyping the molybdenum cofactor sulfurase (MOCOS) gene for a variant allele selected from the group consisting of 2107C>A (exon 11), 509 C>T (exon 4), 1072 G>A (exon 6), 2600T>C (exon 15), 3590>A (exon 4) and a combination thereof.