Pharmacogenetic analysis of the absorption kinetics of cyclosporine in a population of Spanish cardiac transplant patients

BI Tejera, MDA Rubio, J Martínez-Moreno… - Farmacia Hospitalaria …, 2009 - Elsevier
Objective To determine how single nucleotide polymorphisms located on genes MDR1,
CYP3A4, and CYP3A5 affect the absorption kinetics of cyclosporine in cardiac transplant …

Population pharmacokinetics of cyclosporine in kidney and heart transplant recipients and the influence of ethnicity and genetic polymorphisms in the MDR‐1 …

DA Hesselink, T van Gelder… - Clinical …, 2004 - Wiley Online Library
Objective Our objective was to determine the relationship between single nucleotide
polymorphisms (SNPs) in the multidrug resistance 1 (MDR‐1) gene and the cytochrome …

CYP3A5 and MDR1 Genetic Polymorphisms and Cyclosporine Pharmacokinetics After Renal Transplantation

D Anglicheau, E Thervet, I Etienne… - Clinical …, 2004 - Wiley Online Library
Background The immunosuppressive drug cyclosporine (INN, ciclosporin), whose
pharmacokinetic characteristics vary greatly among individuals, is a substrate for …

EFFECTS OF GENETIC POLYMORPHISMS OF CYP3A4, CYP3A5 AND MDR1 ON CYCLOSPORINE PHARMACOKINETICS AFTER RENAL TRANSPLANTATION

YF Hu, W Qiu, ZQ Liu, LJ Zhu, ZQ Liu… - Clinical and …, 2006 - Wiley Online Library
SUMMARY 1 The calcineurin inhibitor cyclosporine is widely used to prevent allograft
rejection after solid organ transplantation. It has a narrow therapeutic index and shows …

MDR1 Haplotypes Do Not Affect the Steady‐State Pharmacokinetics of Cyclosporine in Renal Transplant Patients

I Mai, E Störmer, M Goldammer, A Johne… - The Journal of …, 2003 - Wiley Online Library
This retrospective study investigated the impact of MDR1 haplotypes derived from the single‐
nucleotide polymorphisms (SNPs) 2677G> T (exon 21) and 3435C> T (exon 26) on the …

[PDF][PDF] Association between cyclosporine concentration and genetic polymorphisms of CYP3A5 and MDR1 during the early stage after renal transplantation

N Azarpira, MH Aghdaie… - Exp Clin …, 2006 - researchgate.net
Objectives: Cyclosporine (CsA) has a narrow thera-peutic range, and its pharmacokinetic
characteristics vary among individuals. It also is a substrate for cytochrome P450 (CYP) 3A …

Genetic polymorphisms in MDR1 and CYP3A4 genes in Asians and the influence of MDR1 haplotypes on cyclosporin disposition in heart transplant recipients

B Chowbay, S Cumaraswamy, YB Cheung… - Pharmacogenetics …, 2003 - journals.lww.com
Abstract Intestinal cytochrome P 450 3A4 (CYP3A4) and P-glycoprotein (P-gp) both play a
vital role in the metabolism of oral cyclosporine (CsA). We investigated the genetic …

Association of MDR1, CYP3A4* 18B, and CYP3A5* 3 polymorphisms with cyclosporine pharmacokinetics in Chinese renal transplant recipients

X Qiu, Z Jiao, M Zhang, L Zhong, H Liang, C Ma… - European journal of …, 2008 - Springer
Objective The objective of this study was to retrospectively evaluate the effects of MDR1,
CYP3A4* 18B, and CYP3A5* 3 genetic polymorphisms on cyclosporine A (CsA) …

Contribution of genetic polymorphisms of the CYP3A4, CYP3A5 and MDR1 genes to cyclosporine disposition

Y HU, H Zhou - Chinese Pharmacological Bulletin, 1987 - pesquisa.bvsalud.org
Cyclosporine is an immunosuppressive drug largely used in organ transplantation. It is
characterized by a narrow therapeutic index and wide interindividual variability in its …

CYP3A5 polymorphism effect on cyclosporine pharmacokinetics in living donor renal transplant recipients: analysis by population pharmacokinetics

J Song, MG Kim, B Choi, NY Han… - Annals of …, 2012 - journals.sagepub.com
BACKGROUND: Cyclosporine is often used to prevent allograft rejection in renal transplant
recipients. However, cyclosporine has a narrow therapeutic window and large variability in …