Department of Pharmacy, Shengjing Hospital of China Medical University, Shenyang 110004, China.
Br J Clin Pharmacol. 2009 Sep;68(3):395-401. doi: 10.1111/j.1365-2125.2009.03467.x.
To assess the association between polymorphisms of the ABCB1 gene and the pharmacokinetics of verapamil among healthy Chinese Han ethnic subjects.
Based on polymorphisms of the ABCB1 gene at positions 2677 and 3435, 24 healthy male participants were divided into three groups: 2677GG/3435CC (n = 6), 2677GT/3435CT (n = 12) and 2677TT/3435TT (n = 6). Each subject had received a single oral dose of verapamil (80 mg) under fasting conditions. Multiple blood samples were collected over 24 h, and plasma concentrations of verapamil were determined by HPLC. Pharmacokinetic characteristics were compared between the different genotypic groups.
The pharmacokinetics parameters of verapamil differed significantly among the three genotypic groups. AUC(last) was significantly lower among individuals with the 2677TT/3435TT (159.5 +/- 79.0 ng ml(-1) h) and 2677GT/3435CT (189.3 +/- 73.1 ng ml(-1) h) genotypes than those with the 2677GG/3435CC genotype (303.1 +/- 83.7 ng ml(-1) h) (P= 0.004 and P= 0.008, respectively). However, the CL/F value was higher among subjects with the 2677TT/3435TT (523.0 +/- 173.7 l h(-1)) genotype than those with the 2677GT/3435CT (452.2 +/- 188.6 l h(-1)) or 2677GG/3435CC (265.4 +/- 72.8 l h(-1)) genotypes. A significant difference was also found between the latter two groups (P= 0.034). In addition, the C(max) tended to be higher among subjects with the 2677GG/3435CC genotype than those with the 2677GT/3435CT or 2677TT/3435TT genotypes (42.2 +/- 3.9 vs 32.2 +/- 16.2 vs 38.1 +/- 13.7 ng ml(-1)).
Our study showed for the first time that verapamil pharmacokinetics may be influenced by particular genetic polymorphisms of the ABCB1 gene among healthy Chinese Han ethnic subjects. An individualized dosage regimen design incorporating such information may improve the efficacy of the drug whilst reducing adverse reactions.
评估 ABCB1 基因多态性与健康汉族人群中美托洛尔药代动力学的关系。
根据 ABCB1 基因在 2677 和 3435 位的多态性,将 24 名健康男性参与者分为三组:2677GG/3435CC(n=6)、2677GT/3435CT(n=12)和 2677TT/3435TT(n=6)。每个受试者在空腹状态下单次口服维拉帕米(80mg)。在 24 小时内采集多个血样,并用 HPLC 测定维拉帕米的血浆浓度。比较不同基因型组之间的药代动力学特征。
三组之间维拉帕米的药代动力学参数存在显著差异。2677TT/3435TT(159.5+/-79.0ng/ml/h)和 2677GT/3435CT(189.3+/-73.1ng/ml/h)基因型个体的 AUC(last)明显低于 2677GG/3435CC 基因型个体(303.1+/-83.7ng/ml/h)(P=0.004 和 P=0.008)。然而,2677TT/3435TT 基因型个体的 CL/F 值(523.0+/-173.7l/h)高于 2677GT/3435CT(452.2+/-188.6l/h)或 2677GG/3435CC(265.4+/-72.8l/h)基因型个体。后两者之间也存在显著差异(P=0.034)。此外,2677GG/3435CC 基因型个体的 C(max)值倾向于高于 2677GT/3435CT 或 2677TT/3435TT 基因型个体(42.2+/-3.9 vs 32.2+/-16.2 vs 38.1+/-13.7ng/ml)。
本研究首次表明,在健康汉族人群中,维拉帕米的药代动力学可能受到 ABCB1 基因特定遗传多态性的影响。在药物设计中纳入此类信息的个体化剂量方案可能会提高药物的疗效,同时降低不良反应的发生。