Benefit of Preemptive Pharmacogenetic Information on Clinical Outcome
- PMID: 29377064
- PMCID: PMC6134843
- DOI: 10.1002/cpt.1035
Benefit of Preemptive Pharmacogenetic Information on Clinical Outcome
Abstract
The development of new knowledge around the genetic determinants of variable drug action has naturally raised the question of how this new knowledge can be used to improve the outcome of drug therapy. Two broad approaches have been taken: a point-of-care approach in which genotyping for specific variant(s) is undertaken at the time of drug prescription, and a preemptive approach in which multiple genetic variants are typed in an individual patient and the information archived for later use when a drug with a "pharmacogenetic story" is prescribed. This review addresses the current state of implementation, the rationale for these approaches, and barriers that must be overcome. Benefits to pharmacogenetic testing are only now being defined and will be discussed.
© 2018 American Society for Clinical Pharmacology and Therapeutics.
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References
-
- Rettie AE et al. Hydroxylation of warfarin by human cDNA-expressed cytochrome P-450: a role for P-4502C9 in the etiology of (S)-warfarin-drug interactions. ChemRes Toxicol 5, 54–9 (1992). - PubMed
-
- Rettie AE, Wienkers LC, Gonzalez FJ, Trager WF & Korzekwa KR Impaired (S)-warfarin metabolism catalysed by the R144C allelic variant of CYP2C9. Pharmacogenetics 4, 39–42 (1994). - PubMed
-
- Aithal GP, Day CP, Kesteven PJ & Daly AK Association of polymorphisms in the cytochrome P450 CYP2C9 with warfarin dose requirement and risk of bleeding complications. Lancet 353, 717–9 (1999). - PubMed
-
- Rost S et al. Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2. Nature 427, 537–41 (2004). - PubMed
-
- Rieder MJ et al. Effect of VKORC1 haplotypes on transcriptional regulation and warfarin dose. New England Journal of Medicine 352, 2285–93 (2005). - PubMed
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