Klemetsdal B, Straume B, Wist E, Aarbakke J
Department of Pharmacology, University of Tromsø, Norway.
Eur J Clin Pharmacol. 1993;44(2):147-52. doi: 10.1007/BF00315472.
Red blood cell (RBC) thiopurine methyltransferase (TPMT), an inactivating pathway of 6-mercaptopurine, is controlled by genetic polymorphism and is subject to ethnic variation. RBC TPMT is a good predictor of clinical outcome in children with acute lymphoblastic leukemia. RBC TPMT activity was determined in 226 patients, 176 of them living in northern Norway (of which 123 were Saami (Lapps)). Demographic variables, use of drugs and presence of chronic diseases were evaluated as possible predictors of RBC TPMT activity by a multiple regression model. Men had higher RBC TPMT activity compared to women. Living in the northernmost county of Norway was associated with increased RBC TPMT activity irrespective of ethnicity. The use of diuretics was associated with increased RBC TPMT activity. The gender difference in RBC TPMT activity may indicate a need to treat male subjects more aggressively with thiopurine drugs compared to female subjects.
红细胞(RBC)硫嘌呤甲基转移酶(TPMT)是6-巯基嘌呤的一种失活途径,受基因多态性控制且存在种族差异。RBC TPMT是急性淋巴细胞白血病患儿临床预后的良好预测指标。对226例患者测定了RBC TPMT活性,其中176例生活在挪威北部(其中123例为萨米人(拉普人))。通过多元回归模型评估人口统计学变量、药物使用情况和慢性病的存在作为RBC TPMT活性可能的预测因素。男性的RBC TPMT活性高于女性。无论种族如何,生活在挪威最北部的郡与RBC TPMT活性增加有关。使用利尿剂与RBC TPMT活性增加有关。RBC TPMT活性的性别差异可能表明与女性相比,对男性受试者使用硫嘌呤药物时需要更积极地治疗。