The DOI matches its Crossref record; 54 of the 54 references it cites were found in a registry or an index.
Different Effects of SLCO1B1 Polymorphism on the Pharmacokinetics of Atorvastatin and Rosuvastatin
Abstract
Thirty-two healthy volunteers with different SLCO1B1 genotypes ingested a 20 mg dose of atorvastatin and 10 mg dose of rosuvastatin with a washout period of 1 week. Subjects with the SLCO1B1 c.521CC genotype (n=4) had a 144% (P<0.001) or 61% (P=0.049) greater mean area under the plasma atorvastatin concentration-time curve from 0 to 48 h (AUC(0-48 h)) than those with the c.521TT (n=16) or c.521TC (n=12) genotype, respectively. The AUC(0-48 h) of 2-hydroxyatorvastatin was 100% greater in subjects with the c.521CC genotype than in those with the c.521TT genotype (P=0.018). Rosuvastatin AUC(0-48 h) and peak plasma concentration (Cmax) were 65% (P=0.002) and 79% (P=0.003) higher in subjects with the c.521CC genotype than in those with the c.521TT genotype. These results indicate that, unexpectedly, SLCO1B1 polymorphism has a larger effect on the AUC of atorvastatin than on the more hydrophilic rosuvastatin.
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Metadata
- Authors
- Pasanen, M. K., Fredrikson, H., Neuvonen, P. J., & Niemi, M.
- Venue
- Clinical Pharmacology & Therapeutics
- Publisher
- Wiley
- Published
- 2007-05-02
- Volume
- 82
- Issue
- 6
- Pages
- 726-733
- ISSN
- 0009-9236 (ISSN-L)
- 1532-6535
- OpenAlex
- W2152218609
- Cited by
- 432
- References
- 54
- FWCI
- 19.65
- Type
- journal article
- Language
- en
- Open access
- closed
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- Pasanen, M. K., Fredrikson, H., Neuvonen, P. J., & Niemi, M. (2007). Different Effects of SLCO1B1 Polymorphism on the Pharmacokinetics of Atorvastatin and Rosuvastatin. Clinical Pharmacology & Therapeutics. https://doi.org/10.1038/sj.clpt.6100220
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