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. 2008 Jul 25;66(4):517–528. doi: 10.1111/j.1365-2125.2008.03248.x

Table 4.

Significance of the association of 6-MP metabolite concentrations summary measures with XO, TPMT or ITPA variant genotypes in (a) ALL patients and (b) IBD patients treated with 6-MP/AZA*

(a) ALL patients genotype AUC of RBC metabolite concentrations (AUC1–4 months)
6-TGNs 6-mMPNs 6-TU 6-MP
TPMT*3 heterozygote 0.021 0.008 0.021 0.041
ITPA C94A heterozygote 0.439 0.972 0.950 0.359
ITPA IVS2+21AC mutant 0.008 0.660 0.660 0.660
(b)IBD patients Genotype Mean RBC metabolite concentrations
6-TGNs 6-mMPNs 6-TU 6-MP
XO heterozygote 0.337 0.670 0.497 0.060
TPMT*3 heterozygote 0.866 0.038 0.187 0.670
ITPA C94A mutant 0.670 0.154 0.822 0.497
ITPA IVS2+21AC mutant 0.047 0.960 0.305 0.427
*

Numbers represent P-values for the corresponding association adjusted as per the Bonferroni justification for multiple testing.

Mutant refers to any mutant (homozygote or heterozygote). 6-MP, 6-mercaptopurine; XO, xanthine oxidase; TPMT, thiopurine S-methyl transferase; ITPA, inosine triphosphatase; ALL, acute lymphoblastic leukaemia; IBD, inflammatory bowel disease; AZA, azathioprine; 6-TGN, 6-thioguanine nucleotide; 6-mMPN, 6-methylmercaptopurine nucleotide; 6-TU, 6-thiouric acid.