Mistaken identity: misclassification of TPMT phenotype following blood transfusion

被引:32
作者
Cheung, ST [1 ]
Allan, RN [1 ]
机构
[1] Queen Elizabeth Hosp, Gastroenterol Unit, Birmingham B15 2TH, W Midlands, England
关键词
azathioprine; thiopurine methyltransferase; inflammatory bowel disease; ulcerative colitis; blood transfusion; myelosuppression;
D O I
10.1097/00042737-200311000-00016
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Azathioprine (AZA) is an effective treatment for inflammatory bowel disease. The measurement of thiopurine methyltransferase (TPMT) activity levels helps to identify the one in 300 patients who are at risk of profound myelosuppression with standard doses of AZA. Thus, it is important that the measurement of TPMT activity is accurate. We report a case of misclassification of TPMT phenotype caused by prior blood transfusion. The patient appeared to have an intermediate level of TPMT enzyme activity as measured after the blood transfusion, However, following severe myelosuppression soon after starting AZA, her genotype was determined, which showed that she was homozygous for low TPMT activity. This report reviews some of the limitations in determining both the phenotype and the genotype of TPMT, especially following recent blood transfusion. The dilemma of whether or not to wait for the TPMT activity result before starting AZA is also discussed. (C) 2003 Lippincott Williams Wilkins.
引用
收藏
页码:1245 / 1247
页数:3
相关论文
共 22 条
[1]  
ANSTEY A, 1992, J ROY SOC MED, V85, P752
[2]   REMEDIABLE DEFECTS IN CROHN DISEASE - PROSPECTIVE STUDY OF 63 PATIENTS [J].
BEEKEN, WL .
ARCHIVES OF INTERNAL MEDICINE, 1975, 135 (05) :686-690
[3]   THE IMPORTANCE OF THIOPURINE METHYLTRANSFERASE ACTIVITY FOR THE USE OF AZATHIOPRINE IN TRANSPLANT RECIPIENTS [J].
CHOCAIR, PR ;
DULEY, JA ;
SIMMONDS, HA ;
CAMERON, JS .
TRANSPLANTATION, 1992, 53 (05) :1051-1056
[4]   Genotypic analysis of thiopurine S-methyltransferase in patients with Crohn's disease and severe myelosuppression during azathioprine therapy [J].
Colombel, JF ;
Ferrari, N ;
Debuysere, H ;
Marteau, P ;
Gendre, JP ;
Bonaz, B ;
Soulé, JC ;
Modgliani, R ;
Touze, Y ;
Catala, P ;
Libersa, C ;
Broly, F .
GASTROENTEROLOGY, 2000, 118 (06) :1025-1030
[5]  
COLONNA T, 1994, AM J GASTROENTEROL, V89, P362
[6]   BONE-MARROW TOXICITY CAUSED BY AZATHIOPRINE IN INFLAMMATORY BOWEL-DISEASE - 27 YEARS OF EXPERIENCE [J].
CONNELL, WR ;
KAMM, MA ;
RITCHIE, JK ;
LENNARDJONES, JE .
GUT, 1993, 34 (08) :1081-1085
[7]   Anemia in patients with chronic inflammatory bowel disease [J].
Cronin, CC ;
Shanahan, F .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2001, 96 (08) :2296-2298
[8]   The efficacy of azathioprine for the treatment of inflammatory bowel disease: a 30 year review [J].
Fraser, AG ;
Orchard, TR ;
Jewell, DP .
GUT, 2002, 50 (04) :485-489
[9]   Intravenous iron and erythropoietin for anemia associated with Crohn disease - A randomized, controlled trial [J].
Gasche, C ;
Dejaco, C ;
Waldhoer, T ;
Tillinger, W ;
Reinisch, W ;
Fueger, GF ;
Gangl, A ;
Lochs, H .
ANNALS OF INTERNAL MEDICINE, 1997, 126 (10) :782-787
[10]   Erythrocyte thiopurine methyl transferase assessment prior to azathioprine use in the UK [J].
Holme, SA ;
Duley, JA ;
Sanderson, J ;
Routledge, PA ;
Anstey, AV .
QJM-AN INTERNATIONAL JOURNAL OF MEDICINE, 2002, 95 (07) :439-444