4.2 Article

OATP1B1 388A>G polymorphism and pharmacokinetics of pitavastatin in Chinese healthy volunteers

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WILEY
DOI: 10.1111/j.1365-2710.2009.01071.x

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liquid chromatography-mass spectrometry; organic anion transporting polypeptide 1B1; pharmacokinetic; pitavastatin; polymorphism; 388A > G

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P>Purpose: To investigate the contribution of the most frequent single nucleotide polymorphism (SNPs) of the organic anion transporting polypeptide 1B1 (OATP1B1) 388A > G to the pharmacokinetics of pitavastatin in Chinese healthy volunteers. Methods: Eighteen healthy volunteers participated in this study. Group 1 consisted of nine subjects who were of 388AA wild-type OATP1B1 genotype. Group 2 consisted of seven subjects with the 388GA genotype and two 388GG homozygotes. Two milligram of pitavastatin was administered orally to the volunteers. The plasma concentration of pitavastatin was measured for up to 48 h by liquid chromatography-mass spectrometry (LC-MS). Results: The pharmacokinetic parameters of pitavastatin were significantly different between the two genotyped groups. The concentration (C-max) value was higher in the 388GA + 388GG group than that in the 388AA group (39 center dot 22 +/- 8 center dot 45 vs. 22 center dot 90 +/- 4 center dot 03 ng/mL, P = 0 center dot 006). The area under the curve to the last measurable concentration (AUC(0-48)) and area under the curve extrapolated to infinity (AUC(0-infinity)) of pitavastatin were lower in the 388AA group than in the 388GA + 388GG group (100 center dot 42 +/- 21 center dot 19 vs. 182 center dot 19 +/- 86 center dot 46 ng h/mL, P = 0 center dot 024; 108 center dot 12 +/- 24 center dot 94 vs. 199 center dot 64 +/- 98 center dot 70ng h/mL, P = 0 center dot 026) respectively. The oral clearance (Cl/F) was lower in the 388GA + 388GG group than that in the 388AA group (12 center dot 46 +/- 4 center dot 79 vs. 19 center dot 21 +/- 3 center dot 74/h, P = 0 center dot 012). The elimination of half-life (t(1/2)) and peak concentration times (T-max) values showed no difference between these groups. Conclusions: The OATP 388A > G polymorphism causes significant alterations in the pharmacokinetics of pitavastatin in healthy Chinese volunteers and this may well be clinically significant.

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