de Leon Jose
University of Kentucky, Mental Health Research Center at Eastern State Hospital, 627 West Fourth St., Lexington, KY 40508, USA.
Expert Rev Mol Diagn. 2006 May;6(3):277-86. doi: 10.1586/14737159.6.3.277.
The US FDA has granted market approval for the first pharmacogenetic test using a DNA microarray, the AmpliChip CYP450, which genotypes cytochrome P450 (CYP)2D6 and CYP2C19. The test uses software to predict phenotypes and tests for 27 CYP2D6 alleles, including the deletions and duplications, and three CYP2C19 alleles. Other DNA microarray platforms are being developed for CYP testing, but none have been completely developed or approved by the FDA to date. The differences between an implementation of pharmacogenetic tests centered on the individual and implementation using a public health approach are discussed. In this review, the major obstacles to the wide implementation of pharmacogenetic testing in the clinical environment are summarized.
美国食品药品监督管理局(FDA)已批准首款使用DNA微阵列的药物遗传学检测产品——AmpliChip CYP450,该产品可对细胞色素P450(CYP)2D6和CYP2C19进行基因分型。该检测使用软件预测表型,并检测27个CYP2D6等位基因,包括缺失和重复的等位基因,以及3个CYP2C19等位基因。其他用于CYP检测的DNA微阵列平台正在研发中,但截至目前,尚无产品完全研发完成或获得FDA批准。本文讨论了以个体为中心的药物遗传学检测实施方式与采用公共卫生方法实施检测之间的差异。在这篇综述中,总结了在临床环境中广泛开展药物遗传学检测的主要障碍。