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具有分子病理学药物遗传学工作组 2 级状态的参考物质的特征:CYP2C9、CYP2C19、VKORC1、CYP2C 簇变异体和 GGCX:GeT-RM 协作项目。

Characterization of Reference Materials with an Association for Molecular Pathology Pharmacogenetics Working Group Tier 2 Status: CYP2C9, CYP2C19, VKORC1, CYP2C Cluster Variant, and GGCX: A GeT-RM Collaborative Project.

机构信息

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.

RPRD Diagnostics, Milwaukee, Wisconsin; Department of Pediatrics, Section on Genomic Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin.

出版信息

J Mol Diagn. 2021 Aug;23(8):952-958. doi: 10.1016/j.jmoldx.2021.04.012. Epub 2021 May 19.

Abstract

Pharmacogenetic testing is increasingly available from clinical and research laboratories. However, only a limited number of quality control and other reference materials are currently available for many of the variants that are tested. The Association for Molecular Pathology Pharmacogenetic Work Group has published a series of papers recommending alleles for inclusion in clinical testing. Several of the alleles were not considered for tier 1 because of a lack of reference materials. To address this need, the Division of Laboratory Systems, Centers for Disease Control and Prevention-based Genetic Testing Reference Material (GeT-RM) program, in collaboration with members of the pharmacogenetic testing and research communities and the Coriell Institute for Medical Research, has characterized 18 DNA samples derived from Coriell cell lines. DNA samples were distributed to five volunteer testing laboratories for genotyping using three commercially available and laboratory developed tests. Several tier 2 variants, including CYP2C9∗13, CYP2C19∗35, the CYP2C cluster variant (rs12777823), two variants in VKORC1 (rs61742245 and rs72547529) related to warfarin resistance, and two variants in GGCX (rs12714145 and rs11676382) related to clotting factor activation, were identified among these samples. These publicly available materials complement the pharmacogenetic reference materials previously characterized by the GeT-RM program and will support the quality assurance and quality control programs of clinical laboratories that perform pharmacogenetic testing.

摘要

临床和研究实验室越来越多地提供遗传药理学检测。然而,目前许多经过测试的变体只有有限数量的质量控制和其他参考材料可用。分子病理学协会遗传药理学工作组已经发表了一系列论文,推荐了用于临床检测的等位基因。由于缺乏参考材料,有几个等位基因未被考虑列入第一级。为了解决这一需求,疾病预防控制中心基于实验室系统分部的遗传检测参考材料(GeT-RM)计划与遗传药理学检测和研究界成员以及科里尔医学研究所合作,对 18 个源自科里尔细胞系的 DNA 样本进行了特征描述。将 DNA 样本分发给五家志愿测试实验室,使用三种市售和实验室开发的测试进行基因分型。在这些样本中发现了几个二级变体,包括 CYP2C9∗13、CYP2C19∗35、CYP2C 簇变体(rs12777823)、与华法林抵抗相关的 VKORC1 中的两个变体(rs61742245 和 rs72547529)以及与凝血因子激活相关的 GGCX 中的两个变体(rs12714145 和 rs11676382)。这些公开可用的材料补充了 GeT-RM 计划之前特征描述的遗传药理学参考材料,并将支持进行遗传药理学检测的临床实验室的质量保证和质量控制计划。

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