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Kirchheiner J, Tsahuridu M, Jabrane W, et al. The CYP2C9 polymorphism: from enzyme kinetics to clinical dose recommendations. Per Med. 2004;1(1):63-84doi: 10.1517/17410541.1.1.63.
Kirchheiner, J., Tsahuridu, M., Jabrane, W., Roots, I., & Brockmöller, J. (2004). The CYP2C9 polymorphism: from enzyme kinetics to clinical dose recommendations. Personalized medicine, 1(1), 63-84. https://doi.org/10.1517/17410541.1.1.63
Kirchheiner, Julia, et al. "The CYP2C9 polymorphism: from enzyme kinetics to clinical dose recommendations." Personalized medicine vol. 1,1 (2004): 63-84. doi: https://doi.org/10.1517/17410541.1.1.63
Kirchheiner J, Tsahuridu M, Jabrane W, Roots I, Brockmöller J. The CYP2C9 polymorphism: from enzyme kinetics to clinical dose recommendations. Per Med. 2004 Dec;1(1):63-84. doi: 10.1517/17410541.1.1.63. PMID: 29793229.
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Per Med. 2004 Dec;1(1):63-84. doi: 10.1517/17410541.1.1.63.

The CYP2C9 polymorphism: from enzyme kinetics to clinical dose recommendations.

Personalized medicine

Julia Kirchheiner, Martina Tsahuridu, Wafaa Jabrane, Ivar Roots, Jürgen Brockmöller

Affiliations

  1. University of Cologne, Department of Pharmacology, University of Cologne, Gleueler Str. 24, 50931 Koln, Germany. [email protected].
  2. Humboldt University, Institute of Clinical Pharmacology, University Medical Center Charité, Humboldt University Berlin, Germany.
  3. University of Cologne, Department of Pharmacology, University of Cologne, Gleueler Str. 24, 50931 Koln, Germany.
  4. Georg August University, Department of Clinical Pharmacology, Georg August University Gottingen, Germany.

PMID: 29793229 DOI: 10.1517/17410541.1.1.63

Abstract

CYP2C9 is the major human enzyme of the cytochrome P450 2C subfamily and metabolizes approximately 10% of all therapeutically relevant drugs. Two inherited SNPs termed CYP2C9*2 (Arg144Cys) and *3 (Ile359Leu) are known to affect catalytic function. Numerous rare or functionally silent polymorphisms have been identified. About 35% of the Caucasian population carries at least one *2 or *3 allele. CYP2C9 metabolizes several oral hypoglycemics, oral anticoagulants, non-steroidal anti-inflammatory drugs and other drugs, including phenytoin, losartan, fluvastatin, and torsemide. In vitro studies with several drugs indicate that the Cys144 (.2) and Leu359 (.3) variants confer only about 70 and 10% of the intrinsic clearance of the wild-type protein (.1), respectively. The clinical pharmacokinetic implications of these polymorphisms vary depending on the enzymes contribution to total oral clearance. Several studies demonstrated that the CYP2C9 polymorphisms are medically important for non-steroidal anti-inflammatory drugs, for oral hypoglycemics, vitamin K antagonistic oral anticoagulants, and phenytoin. In particular, CYP2C9 polymorphisms should be routinely considered in therapy with oral anticoagulants where severe adverse events at initiation of therapy might be reduced by genotyping. CYP2C9 polymorphisms were also clinically associated with side effects of phenytoin, with gastric bleeding during therapy with non-steroidals and with hypoglycemia under oral hypoglycemic drugs. Data appear mature enough for the routine consideration of CYP2C9 genotypes in therapy with acenocoumarol, phenytoin, warfarin, and some other drugs. Nevertheless, it is advisable before the routine clinical use of these genotype data to rigorously test the benefits of genotype-based therapeutic recommendations by randomized controlled clinical trials.

Keywords: CYP2C9; cytochrome P450; individualization; pharmacogenetics; pharmacogenetics-based dose adjustment

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