How common are drug and gene interactions? Prevalence in a sample of 1143 patients with CYP2C9, CYP2C19 and CYP2D6 genotyping

被引:84
|
作者
Verbeurgt, Paul [1 ]
Mamiya, Tyler [1 ]
Oesterheld, Jessica [1 ]
机构
[1] Genelex Corp, Seattle, WA 98121 USA
关键词
CYP2C19; CYP2C9; CYP2D6; CYP450; cytochrome; drug interactions; drug-drug; drug-gene; personalized medicine; pharmacogenomics; polymorphism; HOSPITALIZED-PATIENTS; CYTOCHROME-P450; PHARMACOGENOMICS; IMPACT; UNITS;
D O I
10.2217/pgs.14.6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aim: Drug-drug interactions (DDIs) are a widely recognized major cause of adverse drug reactions, but two other newly described important types of interactions also exist: drug-gene interactions (DGIs) and drug-drug-gene interactions (DDGIs). A drug-gene interaction occurs when a patient's genetic CYP450 type (e.g., CYP2D6 poor metabolizer) affects that patient's ability to clear a drug. A drug-drug-gene interaction occurs when the patient's CYP450 genotype and another drug in the patient's regimen (e.g., a CYP2D6 inhibitor) affect that individual's ability to clear a drug. Their prevalence has not been previously described. This pilot study investigates the frequency of DDIs, DGIs and DDGIs in a sample of CYP450 tested individuals. Materials & methods: The investigators conducted a retrospective analysis of 1143 individuals with known CYP2D6, CYP2C19 and CYP2C9 genotypes. Using the individuals' medication lists and YouScript((R)), a software tool to analyze cumulative DDIs and DGIs, the prevalence of DDI, DGI and DDGIs was analyzed. Results: A total of 1053 potential major or substantial interactions were identified in 501 individuals. DDIs accounted for 66.1% of the total interactions. The remaining 33.9% of interactions were DGIs (14.7%) and DDGIs (19.2%). When compared with DDIs alone, DGIs and DDGIs increased the total number of potentially clinically significant interactions by 51.3%. Conclusion: In the future, identifying DGIs and DDGIs may lead to a more comprehensive method of identifying individuals who are at risk for adverse drug reactions. Original submitted 3 May 2013; Revision submitted 6 January 2014
引用
收藏
页码:655 / 665
页数:11
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