Tamminga W J, Wemer J, Oosterhuis B, Weiling J, Wilffert B, de Leij L F, de Zeeuw R A, Jonkman J H
Pharma Bio-Research International B.V., Zuidlaren, The Netherlands.
Eur J Clin Pharmacol. 1999 May;55(3):177-84. doi: 10.1007/s002280050615.
We examined a large database containing results on CYP2D6 and CYP2C19 activity of 4301 Dutch volunteers phenotyped in the context of various clinical pharmacology studies.
The subjects were given 22 mg dextromethorphan, 100 mg mephenytoin and 200 mg caffeine. For CYP2D6, the dextromethorphan/dextrorphan metabolic ratios in urine samples taken for a subsequent 8 h were used. Dextromethorphan and dextrorphan were quantified by reversed-phase high performance liquid chromatography. For CYP2C19 similarly obtained (R)-mephenytoin and (S)-mephenytoin ratios were used. (S)-mephenytoin and (R)-mephenytoin were analysed and quantified by enantioselective capillary gas chromatography. In addition, CYP2C19 poor metabolizer (PM) subjects were reanalysed after acidic pre-treatment of urine samples to confirm the PM status.
The investigated population mainly comprised Caucasian (98.9%) males (68%). The age ranged from 18 to 82 years. For CYP2D6, it was found that 8.0% of the subjects were PMs. The average metabolic ratio was 0.014 (0.033) for subjects who showed extensive metabolizing activity (EM) and 5.4 (7.6) for PM subjects. For CYP2C19, it was found that 1.8% of the subjects were PMs. The metabolic ratio was 0.162 (0.124) for EM subjects and 1.076 (0.040) for PM subjects. Within the EM group the metabolic ratio in females was significantly lower for CYP2D6 (-20%) and significantly higher for CYP2C19 (+40%) compared with males. For PMs there was no such difference for CYP2D6 (P = 0.79) or CYP2C19 (P = 0.20). Oral contraceptive (OC) use significantly decreased the CYP2C19 activity by 68% for mephenytoin as compared to non-OC using females.
For CYP2D6, the PM incidence (8.0%) is in accordance with literature data. The CYP2C19, PM incidence (1.8%) is low compared to reports from other European countries. For mephenytoin, the acidification procedure has been shown to be very important for the confirmation of CYP2C19 PMs. In EM females compared to EM males, CYP2D6 activity is increased and CYP2C19 activity is reduced. For CYP2C19 in particular this reduction is substantial and most pronounced in the age range from 18 to 40 years. For CYP2C19, the reduced activity is associated with the use of oral contraceptives.
我们研究了一个大型数据库,其中包含4301名荷兰志愿者在各种临床药理学研究背景下的CYP2D6和CYP2C19活性结果。
受试者服用22毫克右美沙芬、100毫克美芬妥英和200毫克咖啡因。对于CYP2D6,使用随后8小时采集的尿液样本中的右美沙芬/右啡烷代谢比值。右美沙芬和右啡烷通过反相高效液相色谱法定量。对于CYP2C19,同样使用获得的(R)-美芬妥英和(S)-美芬妥英比值。(S)-美芬妥英和(R)-美芬妥英通过对映体选择性毛细管气相色谱法进行分析和定量。此外,对尿液样本进行酸性预处理后,对CYP2C19慢代谢者(PM)受试者进行重新分析以确认PM状态。
所研究的人群主要为白种人(98.9%)男性(68%)。年龄范围为18至82岁。对于CYP2D6,发现8.0%的受试者为PM。表现出广泛代谢活性(EM)的受试者的平均代谢比值为0.014(0.033),PM受试者为5.4(7.6)。对于CYP2C19,发现1.8%的受试者为PM。EM受试者的代谢比值为0.162(0.124),PM受试者为1.零76(0.040)。在EM组中,与男性相比,女性CYP2D6的代谢比值显著降低(-20%),CYP2C19的代谢比值显著升高(+40%)。对于PM,CYP2D6(P = 0.79)或CYP2C19(P = 0.20)没有这种差异。与未使用口服避孕药的女性相比,使用口服避孕药(OC)使美芬妥英的CYP2C19活性显著降低68%。
对于CYP2D6,PM发生率(8.0%)与文献数据一致。与其他欧洲国家的报告相比,CYP2C19的PM发生率(1.8%)较低。对于美芬妥英,酸化程序已被证明对确认CYP2C19 PM非常重要。与EM男性相比,EM女性的CYP2D6活性增加,CYP2C19活性降低。特别是对于CYP2C19,这种降低幅度很大,在18至40岁年龄范围内最为明显。对于CYP2C19,活性降低与口服避孕药的使用有关。