Department of Pharmaceutical Sciences, College of Pharmacy and Pharmaceutical Sciences, Washington State University, Spokane, Washington, USA.
Department of Pharmacotherapy, College of Pharmacy and Pharmaceutical Sciences, Washington State University, Spokane, Washington, USA.
Clin Transl Sci. 2019 Jan;12(1):39-46. doi: 10.1111/cts.12598. Epub 2018 Nov 26.
The caffeine metabolic ratio is an established marker for cytochrome P450 (CYP) 1A2 activity. Optimal sample size calculation for clinical pharmacokinetic xenobiotic-caffeine interaction studies requires robust estimates of interindividual and intraindividual variation in this ratio. Compared with interindividual variation, factors contributing to intraindividual variation are less defined. An exploratory analysis involving healthy nonsmoking non-naïve caffeine drinkers (1-3 cups/day; 12 men, 12 women) administered caffeine (160 mg) on five occasions evaluated the effects of CYP1A2 induction status (based on genotype) and other factors on intraindividual variation in CYP1A2 activity. Results were compared with those from previous studies. Regardless of whether a hyperinducer (CYP1A21A/1F or CYP1A21F/1F) or normal metabolizer (CYP1A21A/1A, CYP1A21C/1F, or CYP1A21C1F/1C1F), sex, age, oral contraceptive use by women, and smoking status, intraindividual variation was ≤30%. A value of 30% is proposed for optimal design of pharmacokinetic xenobiotic-caffeine interaction studies. Prospective studies are needed for confirmation.
咖啡因代谢比是细胞色素 P450(CYP)1A2 活性的既定标志物。临床药代动力学外源-咖啡因相互作用研究的最佳样本量计算需要对该比值的个体间和个体内变异进行稳健估计。与个体间变异相比,导致个体内变异的因素定义较少。一项涉及健康非吸烟非咖啡因初饮者(每天 1-3 杯;12 名男性,12 名女性)的探索性分析,评估了 CYP1A2 诱导状态(基于基因型)和其他因素对 CYP1A2 活性个体内变异的影响。结果与之前的研究进行了比较。无论 CYP1A21A/1F 或 CYP1A21F/1F 是高诱导剂(hyperinducer)还是正常代谢者(CYP1A21A/1A、CYP1A21C/1F 或 CYP1A21C1F/1C1F),性别、年龄、女性使用口服避孕药以及吸烟状态,个体内变异均≤30%。建议 30%的值用于优化药代动力学外源-咖啡因相互作用研究的设计。需要前瞻性研究进行证实。