Evaluation of a Microarray-Based Genotyping Assay for the Rapid Detection of Cytochrome P450 2C19 *2 and *3 Polymorphisms From Whole Blood Using Nanoparticle Probes

被引:14
作者
Buchan, Blake W. [1 ,2 ]
Peterson, Jess F. [1 ]
Cogbill, Christopher H. [1 ]
Anderson, Dennis K. [3 ]
Ledford, Joellen S. [3 ]
White, Mary N. [3 ]
Quigley, Neil B. [3 ]
Jannetto, Paul J. [1 ,2 ]
Ledeboer, Nathan A. [1 ,2 ]
机构
[1] Med Coll Wisconsin, Dept Pathol, Milwaukee, WI 53226 USA
[2] Dynacare Labs, Milwaukee, WI USA
[3] Mol Pathol Lab Network, Maryville, MO USA
关键词
CYP2C19; Polymorphism; Molecular detection assay; Nanoparticle; CLOPIDOGREL; METABOLISM;
D O I
10.1309/AJCPCPU9Q2IRNYXC
中图分类号
R36 [病理学];
学科分类号
100103 [病原生物学];
摘要
Numerous drugs such as clopidogrel have been developed to reduce coagulation or inhibit platelet function. The hepatic cytochrome P450 (CYP) pathway is involved in the conversion of clopidogrel to its active metabolite. A recent black-box warning was included in the clopidogrel package insert indicating a significant clinical link between specific CYP2C19 genetic variants and poor metabolism of clopidogrel. Of these variants, *2 and *3 are the most common and are associated with complete loss of enzyme activity. In patients who are carriers of a CYP2C19 *2 or *3 allele, the conversion of clopidogrel to its active metabolite may be reduced, which can lead to ischemic events and negative consequence for the patient. We examined the ability of the Verigene CLO assay (Nanosphere, Northbrook, IL) to identify CYP2C19 *2 and *3 polymorphisms in 1,286 unique whole blood samples. The Verigene CLO assay accurately identified homozygous and heterozygous *2 and *3 phenotypes with a specificity of 100% and a final call rate of 99.7%. The assay is fully automated and can produce a result in approximately 3.5 hours.
引用
收藏
页码:604 / 608
页数:5
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