Scott J, Poffenbarger P L
JAMA. 1979 Jul 6;242(1):45-8.
We analyzed the relationship between the pharmacogenetics of tolbutamide metabolism and the controversial University Group Diabetes Program (UGDP) study. Before the institution of that study, the extent of genetic control over the variation in the rate of tolbutamide metabolism was unknown, and all subjects included in the tolbutamide treatment group were given 1,500 mg/day of tolbutamide in a fixed dosage. We addressed the hypothesis that high accrued blood levels of tolbutamide in genetically predisposed slow inactivators might have contributed to the toxic effects reported by the UGDP study. This proposal is based on recent findings from population, twin, and family studies that tolbutamide metabolism is under monogenic control, with nearly one fourth of the population classified as slow inactivators.
我们分析了甲苯磺丁脲代谢的药物遗传学与存在争议的大学组糖尿病计划(UGDP)研究之间的关系。在该研究开展之前,基因对甲苯磺丁脲代谢速率变异的控制程度尚不清楚,且甲苯磺丁脲治疗组纳入的所有受试者均以固定剂量每天服用1500毫克甲苯磺丁脲。我们探讨了这样一种假设,即遗传易感性导致的慢代谢者体内甲苯磺丁脲累积的高血药浓度可能是UGDP研究所报告的毒性作用的原因。这一观点基于近期人群、双胞胎及家族研究的结果,即甲苯磺丁脲代谢受单基因控制,近四分之一的人群被归类为慢代谢者。