Title : Impact of CYP3A4 and MDR1 gene (G2677T) polymorphisms on dose requirement of the cyclosporine in renal transplant Egyptian recipients.

Pub. Date : 2015 Jan

PMID : 25240575






7 Functional Relationships(s)
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1 Impact of CYP3A4 and MDR1 gene (G2677T) polymorphisms on dose requirement of the cyclosporine in renal transplant Egyptian recipients. Cyclosporine ATP binding cassette subfamily B member 1 Homo sapiens
2 Interindividual heterogeneity in expression of ABCB1 and CYP3A4 has been suspected to be one of the factors resulting in cyclosporine (CsA) pharmacokinetic variation. Cyclosporine ATP binding cassette subfamily B member 1 Homo sapiens
3 Interindividual heterogeneity in expression of ABCB1 and CYP3A4 has been suspected to be one of the factors resulting in cyclosporine (CsA) pharmacokinetic variation. Cyclosporine ATP binding cassette subfamily B member 1 Homo sapiens
4 This study aimed to investigate the impact of inter-individual CYP3A4 rs4646437C>T and MDR1 G2677T/A polymorphisms on cyclosporine dose requirements among a sample of renal transplant Egyptian recipients. Cyclosporine ATP binding cassette subfamily B member 1 Homo sapiens
5 Fifty adult Egyptian patients on CsA were genotyped for CYP3A4 rs4646437C>T and MDR1 G2677T/A and correlated with CsA dose requirement and dose-adjusted CsA (C0) blood levels at 3, 6, and 9 months post transplantation. Cyclosporine ATP binding cassette subfamily B member 1 Homo sapiens
6 Fifty adult Egyptian patients on CsA were genotyped for CYP3A4 rs4646437C>T and MDR1 G2677T/A and correlated with CsA dose requirement and dose-adjusted CsA (C0) blood levels at 3, 6, and 9 months post transplantation. Cyclosporine ATP binding cassette subfamily B member 1 Homo sapiens
7 Genotyping of both CYP3A4 and MDR1 SNPs may be helpful in providing pre-transplant pharmacogenetic information to individualize CsA dosing. Cyclosporine ATP binding cassette subfamily B member 1 Homo sapiens