Title : Effect of CYP3A4 and CYP3A5 Genetic Polymorphisms on the Pharmacokinetics of Sirolimus in Healthy Chinese Volunteers.

Pub. Date : 2017 Aug

PMID : 28700521






6 Functional Relationships(s)
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1 Effect of CYP3A4 and CYP3A5 Genetic Polymorphisms on the Pharmacokinetics of Sirolimus in Healthy Chinese Volunteers. Sirolimus cytochrome P450 family 3 subfamily A member 4 Homo sapiens
2 Sirolimus is primarily metabolized by cytochrome CYP3A4 and CYP3A5. Sirolimus cytochrome P450 family 3 subfamily A member 4 Homo sapiens
3 This study aimed to clarify the effect of CYP3A genetic polymorphisms, including the CYP3A4*1G and CYP3A5*3 polymorphisms, on the pharmacokinetics of sirolimus. Sirolimus cytochrome P450 family 3 subfamily A member 4 Homo sapiens
4 This study aimed to clarify the effect of CYP3A genetic polymorphisms, including the CYP3A4*1G and CYP3A5*3 polymorphisms, on the pharmacokinetics of sirolimus. Sirolimus cytochrome P450 family 3 subfamily A member 4 Homo sapiens
5 CONCLUSIONS: CYP3A4 and CYP3A5 genetic polymorphisms are important factors affecting pharmacokinetic parameters of sirolimus. Sirolimus cytochrome P450 family 3 subfamily A member 4 Homo sapiens
6 Our data support the monitoring of blood sirolimus concentrations, especially in CYP3A5*1 and CYP3A4*1 G carriers, to ensure accurate dosing in the clinical setting. Sirolimus cytochrome P450 family 3 subfamily A member 4 Homo sapiens