DPYD 基因分型建议:分子病理学协会、美国医学遗传学和基因组学学院、临床药物遗传学实施联合会、美国病理学家学会、荷兰皇家药剂师协会荷兰药物遗传学工作组、欧洲药物基因组学和个性化治疗学会、药物基因组学知识库和药物基因变异联合会的联合共识建议。

IF 3.4 3区 医学 Q1 PATHOLOGY Journal of Molecular Diagnostics Pub Date : 2024-07-18 DOI:10.1016/j.jmoldx.2024.05.015
Victoria M. Pratt , Larisa H. Cavallari , Makenzie L. Fulmer , Andrea Gaedigk , Houda Hachad , Yuan Ji , Lisa V. Kalman , Reynold C. Ly , Ann M. Moyer , Stuart A. Scott , Amy J. Turner , Ron H.N. van Schaik , Michelle Whirl-Carrillo , Karen E. Weck
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引用次数: 0

摘要

分子病理学协会(AMP)临床实践委员会药物基因组学(PGx)工作组的目标是定义推荐用于临床检测的药物基因等位基因的关键属性,以及临床 PGx 基因分型检测中应包含的最低变异株集合。本系列文件提供了最低变异等位基因集(第 1 级)和扩展变异等位基因列表(第 2 级)的建议,这将有助于临床实验室设计 PGx 检测方法。AMP PGx 工作组在制定这些建议时考虑了变异等位基因的功能影响、多种族人群中的等位基因频率、参考材料的可用性以及 PGx 检测的其他技术因素。该工作组的目标是促进临床实验室 PGx 检测的标准化。本文件将重点关注可应用于所有 DPD 相关药物的临床 DPYD PGx 检测。这些建议不应被解释为指令性的,而是提供一个参考指南。
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DPYD Genotyping Recommendations

The goals of the Association for Molecular Pathology Clinical Practice Committee's Pharmacogenomics (PGx) Working Group are to define the key attributes of pharmacogenetic alleles recommended for clinical testing and a minimum set of variants that should be included in clinical PGx genotyping assays. This document series provides recommendations for a minimum set of variant alleles (tier 1) and an extended list of variant alleles (tier 2) that will aid clinical laboratories when designing assays for PGx testing. The Association for Molecular Pathology PGx Working Group considered the functional impact of the variant alleles, allele frequencies in multiethnic populations, the availability of reference materials, and other technical considerations for PGx testing when developing these recommendations. The goal of this Working Group is to promote standardization of PGx testing across clinical laboratories. This document will focus on clinical DPYD PGx testing that may be applied to all dihydropyrimidine dehydrogenase–related medications. These recommendations are not to be interpreted as prescriptive but to provide a reference guide.

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来源期刊
CiteScore
8.10
自引率
2.40%
发文量
143
审稿时长
43 days
期刊介绍: The Journal of Molecular Diagnostics, the official publication of the Association for Molecular Pathology (AMP), co-owned by the American Society for Investigative Pathology (ASIP), seeks to publish high quality original papers on scientific advances in the translation and validation of molecular discoveries in medicine into the clinical diagnostic setting, and the description and application of technological advances in the field of molecular diagnostic medicine. The editors welcome for review articles that contain: novel discoveries or clinicopathologic correlations including studies in oncology, infectious diseases, inherited diseases, predisposition to disease, clinical informatics, or the description of polymorphisms linked to disease states or normal variations; the application of diagnostic methodologies in clinical trials; or the development of new or improved molecular methods which may be applied to diagnosis or monitoring of disease or disease predisposition.
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