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.


Journal

The Journal of molecular diagnostics : JMD
ISSN: 1943-7811
Titre abrégé: J Mol Diagn
Pays: United States
ID NLM: 100893612

Informations de publication

Date de publication:
08 2021
Historique:
received: 02 03 2021
revised: 26 03 2021
accepted: 29 04 2021
pubmed: 22 5 2021
medline: 18 1 2022
entrez: 21 5 2021
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 34020041
pii: S1525-1578(21)00121-5
doi: 10.1016/j.jmoldx.2021.04.012
pmc: PMC8491090
pii:
doi:

Substances chimiques

cytochrome P-450 CYP2C subfamily 0
Cytochrome P-450 Enzyme System 9035-51-2
CYP2C9 protein, human EC 1.14.13.-
Cytochrome P-450 CYP2C9 EC 1.14.13.-
CYP2C19 protein, human EC 1.14.14.1
Cytochrome P-450 CYP2C19 EC 1.14.14.1
VKORC1 protein, human EC 1.17.4.4
Vitamin K Epoxide Reductases EC 1.17.4.4
Carboxy-Lyases EC 4.1.1.-
GGCX protein, human EC 4.1.1.-

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

952-958

Subventions

Organisme : NIGMS NIH HHS
ID : R24 GM123930
Pays : United States
Organisme : NHGRI NIH HHS
ID : U01 HG007762
Pays : United States

Informations de copyright

Copyright © 2021 Association for Molecular Pathology and American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.

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Auteurs

Victoria M Pratt (VM)

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

Amy Turner (A)

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

Ulrich Broeckel (U)

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

D Brian Dawson (DB)

Department of Pediatrics, University of Cincinnati, Cincinnati, Ohio; Department of Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, Ohio; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

Andrea Gaedigk (A)

Division of Clinical Pharmacology, Toxicology and Therapeutic Innovation, Children's Mercy Kansas City, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri.

Ty C Lynnes (TC)

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

Elizabeth B Medeiros (EB)

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

Ann M Moyer (AM)

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.

Deborah Requesens (D)

Coriell Institute for Medical Research, Camden, New Jersey.

Francesco Vetrini (F)

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

Lisa V Kalman (LV)

Division of Laboratory Systems, Centers for Disease Control and Prevention, Atlanta, Georgia. Electronic address: LJK0@cdc.gov.

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Classifications MeSH