The utility of 6-thioguanine metabolite levels in managing patients with inflammatory bowel disease

被引:75
作者
Goldenberg, BA [1 ]
Rawsthorne, P [1 ]
Bernstein, CN [1 ]
机构
[1] Univ Manitoba, John Buhler Res Ctr, Inflammatory Bowel Dis Clin & Res Ctr, Winnipeg, MB R3E 3P4, Canada
关键词
D O I
10.1111/j.1572-0241.2004.30415.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVES: We aimed at determining the utility of measuring 6-thioguanine (6-TG) and 6-methylmercaptopurine (6-MMP) in inflammatory bowel disease (IBD) patients on azathioprine (AZA) or 6-mercaptopurine (6-MP), whether the described therapeutic range for 6-TG (235-400 pmol/8 x 10(8) red blood cells, RBC) correlated with clinical remission or leukopenia, and if 6-MMP level was a marker for hepatotoxicity (>5,700 pmol/8 x 10(8) RBC). METHODS: Study eligibility included an IBD diagnosis of >6 months and either active disease or disease remission of <6 months and the use of AZA/6-MP for >10 wk consecutively. Metabolite levels were evaluated against clinical status, CBC, and hepatic parameters. RESULTS: Seventy-four of 166 AZA/6-MP users were eligible. 6-TG levels >235 pmol/8 x 10(8) RBC were found in 22/59 (38%) with active disease and in 7/15 with remission (47%, p = 0.16). There was a trend of higher 6-TG levels among those in remission versus those with active disease (mean 325 +/- 284 vs 223 +/- 159 pmol/8 x 10(8) RBC, p = 0.2). No hepatotoxicity was observed, although 12.2% had 6-MMP levels > 5,700 pmol/8 x 10(8) RBC. The correlation between 6-MP dose and 6-TG levels was weak (r = 0.22, p = 0.08). The 6-TG level did not correlate with WBC. There were five instances, each of markedly low levels of both 6-TG and 6-MMP, suggesting noncompliance and of marked 6-MMP levels versus 6-TG. CONCLUSIONS: There was a poor correlation between 6-TG levels and remission. Nonetheless, the measurements of these levels are helpful when patients are on high doses but not achieving remission since noncompliance or metabolism favoring 6-MMP can be established.
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页码:1744 / 1748
页数:5
相关论文
共 16 条
[1]   Mercaptopurine metabolite results in clinical gastroenterology practice [J].
Bloomfeld, RS ;
Onken, JE .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 17 (01) :69-73
[2]   Utilisation of erythrocyte 6-thioguanine metabolite levels to optimise azathioprine therapy in patients with inflammatory bowel disease [J].
Cuffari, C ;
Hunt, S ;
Bayless, T .
GUT, 2001, 48 (05) :642-646
[3]   Pharmacogenomics and metabolite measurement for 6-mercaptopurine therapy in inflammatory bowel disease [J].
Dubinsky, MC ;
Lamothe, S ;
Yang, HY ;
Targan, SR ;
Sinnett, D ;
Théorêt, Y ;
Seidman, EG .
GASTROENTEROLOGY, 2000, 118 (04) :705-713
[4]   6-thioguanine can cause serious liver injury in inflammatory bowel disease patients [J].
Dubinsky, MC ;
Vasiliauskas, EA ;
Singh, H ;
Abreu, MT ;
Papadakis, KA ;
Tran, T ;
Martin, P ;
Vierling, JM ;
Geller, SA ;
Targan, SR ;
Poordad, FF .
GASTROENTEROLOGY, 2003, 125 (02) :298-303
[5]   6-MP metabolite profiles provide a biochemical explanation for 6-MP resistance in patients with inflammatory bowel disease [J].
Dubinsky, MC ;
Yang, HY ;
Hassard, PV ;
Seidman, EG ;
Kam, LY ;
Abreu, MT ;
Targan, SR ;
Vasiliauskas, EA .
GASTROENTEROLOGY, 2002, 122 (04) :904-915
[6]   A REVERSED PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY APPROACH IN DETERMINING TOTAL RED-BLOOD-CELL CONCENTRATIONS OF 6-THIOGUANINE, 6-MERCAPTOPURINE, METHYLTHIOGUANINE, AND METHYLMERCAPTOPURINE IN A PATIENT RECEIVING THIOPURINE THERAPY [J].
ERDMANN, GR ;
FRANCE, LA ;
BOSTROM, BC ;
CANAFAX, DM .
BIOMEDICAL CHROMATOGRAPHY, 1990, 4 (02) :47-51
[7]   6-mercaptopurine metabolite levels in children with inflammatory bowel disease [J].
Gupta, P ;
Gokhale, R ;
Kirschner, BS .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2001, 33 (04) :450-454
[8]  
HARVEY RF, 1980, LANCET, V1, P1134
[9]   Profile of non-compliance in lymphoblastic leukaemia [J].
Lancaster, D ;
Lennard, L ;
Lilleyman, JS .
ARCHIVES OF DISEASE IN CHILDHOOD, 1997, 76 (04) :365-366
[10]   Measurement of thiopurine methyltransferase activity and azathioprine metabolites in patients with inflammatory bowel disease [J].
Lowry, PW ;
Franklin, CL ;
Weaver, AL ;
Pike, MG ;
Mays, DC ;
Tremaine, WJ ;
Lipsky, JJ ;
Sandborn, WJ .
GUT, 2001, 49 (05) :665-670