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  • [Challenge in genome-wide association study for establishment of personalized medicine: focusing on the pharmacogenomics of warfarin and carbamazepine].

[Challenge in genome-wide association study for establishment of personalized medicine: focusing on the pharmacogenomics of warfarin and carbamazepine].

Rinsho byori. The Japanese journal of clinical pathology (2013-08-21)
Taisei Mushiroda
ABSTRACT

Drug efficacies and adverse drug reactions(ADRs) are often unpredictable, owing to the fact that responses to drugs vary among different individuals; however, it is believed that applying knowledge of pharmacogenomics (PGx) in clinical treatment can help to improve the prediction of drug responses, leading to the establishment of personalized medicine that aims to provide the right drug at the appropriate dose for each individual patient. In recent years, the FDA has recommended the genotyping of polymorphisms in drug-metabolizing enzymes and HLA prior to drug administration to avoid severe ADRs to many drugs, such as carbamazepine and abacavir. A genome-wide association study (GWAS) is useful to identify genomic biomarkers that can predict the efficacy or risk of ADRs to various drugs. In order to apply genomic biomarkers to clinical therapeutics, prospective clinical trials will be necessary to evaluate an intervention based on genetic tests.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Carbamazepine, meets USP testing specifications
Carbamazepine, European Pharmacopoeia (EP) Reference Standard
Supelco
Carbamazepine, analytical standard
USP
Carbamazepine, United States Pharmacopeia (USP) Reference Standard
Supelco
Carbamazepine, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
Carbamazepine solution, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®