Armstrong Victor W, Shipkova Maria, von Ahsen Nicolas, Oellerich Michael
Department of Clinical Chemistry, George-August University, D-37075 Goettingen, Germany.
Ther Drug Monit. 2004 Apr;26(2):220-6. doi: 10.1097/00007691-200404000-00024.
The thiopurine medications 6-mercaptopurine (6-MP), 6-thioguanine (6-TG), and azathioprine are used in treatment of childhood acute lymphoblastic leukemia, autoimmune diseases, and, in the case of azathioprine, in solid organ transplantation. They are converted in vivo to the active 6-thioguanine nucleotides (6-TGN). One person in 300 in white populations has low or undetectable TPMT activity and is at risk for accumulating 6-TGN with the consequence of severe, life-threatening myelosuppression. A rational therapeutic strategy for thiopurine drug use is to first determine TPMT phenotype/genotype and then to adjust the dosage on an individual basis. Determination of erythrocyte 6-TGN levels can further help to optimize therapy. TPMT activity (phenotype) is determined in erythrocytes using radiochemical or HPLC procedures. Recent HPLC procedures show good agreement with the original radiochemical method, while offering simplified sample pretreatment and improved precision. To date, 12 mutant alleles responsible for TPMT deficiency have been published. Restriction fragment length polymorphism PCR and allele-specific PCR have been used for detection of TPMT mutations. Genotyping methods that allow a higher throughput include real-time PCR (LightCycler) and denaturing HPLC. Numerous HPLC methods have been reported for quantification of 6-TGN. The majority involve acid hydrolysis to 6-TG at high temperature. There are substantial differences in the hydrolysis step, extraction procedure, chromatographic conditions and method of detection. Erythrocyte 6-TGN concentrations can vary up to 2.6-fold depending on the HPLC method. The method that has found the greatest application in clinical studies is that of Lennard. This has served as the basis for the establishment of treatment-related therapeutic ranges for thiopurine therapy. These ranges will not necessarily be applicable when other methodology is used. There is an urgent need to harmonize the analytic procedures for 6-TGN.
硫嘌呤类药物6-巯基嘌呤(6-MP)、6-硫鸟嘌呤(6-TG)和硫唑嘌呤用于治疗儿童急性淋巴细胞白血病、自身免疫性疾病,硫唑嘌呤还用于实体器官移植。它们在体内转化为活性6-硫鸟嘌呤核苷酸(6-TGN)。白种人群中每300人中有1人TPMT活性低或检测不到,有蓄积6-TGN的风险,可能导致严重的、危及生命的骨髓抑制。合理使用硫嘌呤类药物的治疗策略是首先确定TPMT表型/基因型,然后根据个体情况调整剂量。测定红细胞6-TGN水平有助于进一步优化治疗。使用放射化学法或高效液相色谱法(HPLC)在红细胞中测定TPMT活性(表型)。最近的HPLC方法与原始放射化学方法结果吻合良好,同时简化了样品预处理并提高了精密度。迄今为止,已公布了12个导致TPMT缺乏的突变等位基因。限制性片段长度多态性PCR和等位基因特异性PCR已用于检测TPMT突变。通量更高的基因分型方法包括实时PCR(LightCycler)和变性HPLC。已有许多HPLC方法用于定量6-TGN。大多数方法涉及在高温下将其酸水解为6-TG。水解步骤、提取程序、色谱条件和检测方法存在很大差异。根据HPLC方法不同,红细胞6-TGN浓度变化可达2.6倍。在临床研究中应用最广泛的方法是Lennard法。这已成为确立硫嘌呤治疗相关治疗范围的基础。当使用其他方法时,这些范围不一定适用。迫切需要统一6-TGN的分析程序。