Effect of ABCB1 (MDR1) haplotypes derived from G2677T/C3435T on the pharmacokinetics of amlodipine in healthy subjects

KA Kim, PW Park, JY Park - British journal of clinical …, 2007 - Wiley Online Library
KA Kim, PW Park, JY Park
British journal of clinical pharmacology, 2007Wiley Online Library
Aim We aimed to investigate the effect of the ABCB1 gene on the pharmacokinetics of
amlodipine. Methods Based on polymorphisms of the ABCB1 gene at positions 2677 and
3435, 26 healthy male participants were divided into three groups: subjects with
2677GG/3435CC (n= 9), 2677GT/3435CT (n= 9) and 2677TT/3435TT (n= 8). After a single‐
dose administration of 5 mg amlodipine, plasma concentrations of amlodipine were
measured and its pharmacokinetic characteristics were compared according to ABCB1 …
Aim
We aimed to investigate the effect of the ABCB1 gene on the pharmacokinetics of amlodipine.
Methods
Based on polymorphisms of the ABCB1 gene at positions 2677 and 3435, 26 healthy male participants were divided into three groups: subjects with 2677GG/3435CC (n = 9), 2677GT/3435CT (n = 9) and 2677TT/3435TT (n = 8). After a single‐dose administration of 5 mg amlodipine, plasma concentrations of amlodipine were measured and its pharmacokinetic characteristics were compared according to ABCB1 genotype.
Results
The area under the plasma concentration–time curve was significantly lower in subjects with 2677TT/3435TT (140.8 ± 35.6 ng h−1 ml−1) and 2677GT/3435CT (149.8 ± 40.1 ng h−1 ml−1) than in those with 2677GG/3435CC (208.6 ± 39.2 ng h−1 ml−1) [95% confidence interval (CI) on the difference, 2677GG/3435CC vs. 2677GT/3435CT 12.0, 105.6, P < 0.01; 2677GG/3435CC vs. 2677TT/3435TT 19.6, 116.0, P < 0.01; 2677GT/3435CT vs. 2677TT/3435TT − 39.2, 57.2, P > 0.05]. The peak plasma concentrations were highest in subjects with 2677GG/3435CC (3.8 ± 0.5 ng ml−1), lower in subjects with 2677GT/3435CT (3.2 ± 0.5 ng ml−1) and 2677TT/3435TT (2.7 ± 0.5 ng ml−1) in rank and showed a significant difference between those with 2677GG/3435CC and with 2677TT/3435TT (95% CI on the difference 0.4, 2.0, P < 0.01). However, the oral clearance was higher in subjects with 2677TT/3435TT (37.7 ± 10.2 l h−1) than in those with 2677GT/3435CT (35.7 ± 9.9 l h−1) and with 2677GG/3435CC (24.8 ± 5.4 l h−1) and exhibited a significant difference between ABCB1 genotype groups (95% CI on the difference, 2677GG/3435CC vs. 2677GT/3435CT − 21.5, − 0.3, P < 0.05; 2677GG/3435CC vs. 2677TT/3435TT − 23.8, − 2.0, P < 0.05).
Conclusion
Amlodipine pharmacokinetics was affected by the genetic polymorphisms of the ABCB1 gene in humans. These findings may provide a plausible explanation for interindividual variation in the disposition of amlodipine, although our study could not explain the exact mechanism(s) by which the polymorphic ABCB1 gene paradoxically reduces the plasma levels of amlodipine. Further evaluation is thus warranted.
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