No significant effect of ABCB1 haplotypes on the pharmacokinetics of fluvastatin, pravastatin, lovastatin, and rosuvastatin

التفاصيل البيبلوغرافية
العنوان: No significant effect of ABCB1 haplotypes on the pharmacokinetics of fluvastatin, pravastatin, lovastatin, and rosuvastatin
المؤلفون: Kaisa J. Kurkinen, Janne T. Backman, Pertti J. Neuvonen, Jenni E. Keskitalo, Mikko Niemi, Mikko Neuvonen
بيانات النشر: Blackwell Science Inc, 2009.
سنة النشر: 2009
مصطلحات موضوعية: Adult, Male, ATP Binding Cassette Transporter, Subfamily B, Indoles, Genotype, Biology, Pharmacology, Polymorphism, Single Nucleotide, Fatty Acids, Monounsaturated, Young Adult, Pharmacokinetics, medicine, Humans, Pharmacology (medical), Rosuvastatin, ATP Binding Cassette Transporter, Subfamily B, Member 1, Lovastatin, Rosuvastatin Calcium, Fluvastatin, Pravastatin, Sulfonamides, Cross-Over Studies, Fluorobenzenes, Pyrimidines, Haplotypes, Simvastatin, Pharmacogenetics, Area Under Curve, HMG-CoA reductase, biology.protein, Female, Lovastatin Acid, Hydroxymethylglutaryl-CoA Reductase Inhibitors, medicine.drug
الوصف: WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT • ABCB1 genotype affects the pharmacokinetics and cholesterol-lowering effects of simvastatin and atorvastatin. • The cholesterol-lowering effect of fluvastatin has been associated with ABCB1 genotype, and pravastatin, lovastatin, lovastatin acid, and rosuvastatin are substrates of ABCB1. • However, it is not known whether ABCB1 genotype affects the pharmacokinetics of fluvastatin, pravastatin, lovastatin, or rosuvastatin. WHAT THIS STUDY ADDS • ABCB1 c.1236C-c.2677G-c.3435C and c.1236T-c.2677T-c.3435T haplotypes have no significant effects on the pharmacokinetics of fluvastatin, pravastatin, lovastatin, or rosuvastatin. AIMS This study aimed to investigate possible effects of ABCB1 genotype on fluvastatin, pravastatin, lovastatin, and rosuvastatin pharmacokinetics. METHODS In a fixed-order crossover study, 10 healthy volunteers with the ABCB1 c.1236C/C-c.2677G/G-c.3435C/C (CGC/CGC) genotype and 10 with the c.1236T/T-c.2677T/T-c.3435T/T (TTT/TTT) genotype ingested a single 20-mg dose of fluvastatin, pravastatin, lovastatin, and rosuvastatin. Plasma fluvastatin, pravastatin, and lovastatin concentrations were measured up to 12 h and plasma and urine rosuvastatin concentrations up to 48 and 24 h, respectively. RESULTS The ABCB1 genotype had no significant effect on the pharmacokinetics of any of the investigated statins. The geometric mean ratio (95% confidence interval) of the area under the plasma concentration–time curve from 0 h to infinity (AUC0–∞) in participants with the TTT/TTT genotype to that in those with the CGC/CGC genotype was 0.96 (0.77, 1.20; P= 0.737) for fluvastatin, 0.92 (0.53, 1.62; P= 0.772) for pravastatin, 0.83 (0.36, 1.90; P= 0.644) for lovastatin, 1.25 (0.72, 2.17; P= 0.400) for lovastatin acid, and 1.10 (0.73, 1.65; P= 0.626) for rosuvastatin. The AUC0–∞ of lovastatin acid correlated significantly with that of rosuvastatin (r= 0.570, P= 0.009), but none of the other AUC0–∞ pairs showed a significant correlation. CONCLUSIONS These data suggest that the ABCB1 c.1236C-c.2677G-c.3435C and c.1236T-c.2677T-c.3435T haplotypes play no significant role in the interindividual variability in the pharmacokinetics of fluvastatin, pravastatin, lovastatin, and rosuvastatin.
اللغة: English
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c629cdae83c49635ab72c30b8dee9105Test
https://europepmc.org/articles/PMC2767284Test/
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....c629cdae83c49635ab72c30b8dee9105
قاعدة البيانات: OpenAIRE