CYP3A4 and CYP3A5 Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, and Pharmacogenomics Knowledgebase
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 a...
Gespeichert in:
Veröffentlicht in: | The Journal of molecular diagnostics : JMD 2023-09, Vol.25 (9), p.619-629 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 629 |
---|---|
container_issue | 9 |
container_start_page | 619 |
container_title | The Journal of molecular diagnostics : JMD |
container_volume | 25 |
creator | Pratt, Victoria M Cavallari, Larisa H Fulmer, Makenzie L Gaedigk, Andrea Hachad, Houda Ji, Yuan Kalman, Lisa V Ly, Reynold C Moyer, Ann M Scott, Stuart A van Schaik, Ron H N Whirl-Carrillo, Michelle Weck, Karen E |
description | 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 panel of variant alleles (tier 1) and an extended panel 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 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 gene/allele testing across clinical laboratories. This document will focus on clinical CYP3A4 and CYP3A5 PGx testing that may be applied to all CYP3A4- and CYP3A5-related medications. These recommendations are not to be interpreted as prescriptive but to provide a reference guide. |
doi_str_mv | 10.1016/j.jmoldx.2023.06.008 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10565868</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2835274167</sourcerecordid><originalsourceid>FETCH-LOGICAL-p182t-f7eebe8b6963ef1c49234efbe4914299eef7a5954314194ad9c995ffc77ca3a73</originalsourceid><addsrcrecordid>eNplkk1z0zAQhg0DQ0vhHzCMjhySYNnyFxcmE0oolCFTyjCcPIq8thVkrZFkINz538hJ20nLSav9eN7dlYLgGQ1nNKTpy81s06Gqfs-iMIpnYToLw_x-cEwLFk-znNIHB_ZR8NjaTRhSxtLoUXAUZ4wWEUuO7_1dfFvFc0a4rsjOTMgSNLptL3VDLkBg14GuuJOo7SsyJ-9RakcW_gbaDvZOCsGauBbI3FoUcu-q0ZCPqEAMihuy4q5Fhc12QhZKaim4IquWm44LbECDk8KSs65X4KFuTxjV0Dg5dL4IlYIGRqF5B8bX6xumtM5OyJvBifZ_5lc038eZlgaH_rrPC9x6_VsVI-Sw_wk5HQz24HU-ex-47W6iAz52I3_c4AqMRc2V_AMVuWzB8N7PuYvcTf-g8ZeCqoE1t_AkeFhzZeHp1XkSfHl7erl4Nz3_tDxbzM-nPc0jN60zgDXk67RIY6ipYEUUM6jXwArKoqIAqDOeFAmLqX9fxqtCFEVS1yLLBI95Fp8Er_fcflh3UAm_YcNV2RvZcbMtkcvydkTLtmzwZ0nDJE3yNPeEF1cEgz8GsK7spBWgFNeAgy2jPE4i_7vSUez5odiNyvXni_8BswjquA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2835274167</pqid></control><display><type>article</type><title>CYP3A4 and CYP3A5 Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, and Pharmacogenomics Knowledgebase</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Pratt, Victoria M ; Cavallari, Larisa H ; Fulmer, Makenzie L ; Gaedigk, Andrea ; Hachad, Houda ; Ji, Yuan ; Kalman, Lisa V ; Ly, Reynold C ; Moyer, Ann M ; Scott, Stuart A ; van Schaik, Ron H N ; Whirl-Carrillo, Michelle ; Weck, Karen E</creator><creatorcontrib>Pratt, Victoria M ; Cavallari, Larisa H ; Fulmer, Makenzie L ; Gaedigk, Andrea ; Hachad, Houda ; Ji, Yuan ; Kalman, Lisa V ; Ly, Reynold C ; Moyer, Ann M ; Scott, Stuart A ; van Schaik, Ron H N ; Whirl-Carrillo, Michelle ; Weck, Karen E</creatorcontrib><description>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 panel of variant alleles (tier 1) and an extended panel 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 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 gene/allele testing across clinical laboratories. This document will focus on clinical CYP3A4 and CYP3A5 PGx testing that may be applied to all CYP3A4- and CYP3A5-related medications. These recommendations are not to be interpreted as prescriptive but to provide a reference guide.</description><identifier>ISSN: 1943-7811</identifier><identifier>ISSN: 1525-1578</identifier><identifier>EISSN: 1943-7811</identifier><identifier>DOI: 10.1016/j.jmoldx.2023.06.008</identifier><identifier>PMID: 37419245</identifier><language>eng</language><publisher>United States: American Society for Investigative Pathology</publisher><subject>Consensus ; Cytochrome P-450 CYP3A - genetics ; Genotype ; Humans ; Pathologists ; Pathology, Molecular ; Pharmacists ; Pharmacogenetics ; Special</subject><ispartof>The Journal of molecular diagnostics : JMD, 2023-09, Vol.25 (9), p.619-629</ispartof><rights>Copyright © 2023 Association for Molecular Pathology and American Society for Investigative Pathology. All rights reserved.</rights><rights>2023 Association for Molecular Pathology and American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved. 2023 Association for Molecular Pathology and American Society for Investigative Pathology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37419245$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pratt, Victoria M</creatorcontrib><creatorcontrib>Cavallari, Larisa H</creatorcontrib><creatorcontrib>Fulmer, Makenzie L</creatorcontrib><creatorcontrib>Gaedigk, Andrea</creatorcontrib><creatorcontrib>Hachad, Houda</creatorcontrib><creatorcontrib>Ji, Yuan</creatorcontrib><creatorcontrib>Kalman, Lisa V</creatorcontrib><creatorcontrib>Ly, Reynold C</creatorcontrib><creatorcontrib>Moyer, Ann M</creatorcontrib><creatorcontrib>Scott, Stuart A</creatorcontrib><creatorcontrib>van Schaik, Ron H N</creatorcontrib><creatorcontrib>Whirl-Carrillo, Michelle</creatorcontrib><creatorcontrib>Weck, Karen E</creatorcontrib><title>CYP3A4 and CYP3A5 Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, and Pharmacogenomics Knowledgebase</title><title>The Journal of molecular diagnostics : JMD</title><addtitle>J Mol Diagn</addtitle><description>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 panel of variant alleles (tier 1) and an extended panel 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 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 gene/allele testing across clinical laboratories. This document will focus on clinical CYP3A4 and CYP3A5 PGx testing that may be applied to all CYP3A4- and CYP3A5-related medications. These recommendations are not to be interpreted as prescriptive but to provide a reference guide.</description><subject>Consensus</subject><subject>Cytochrome P-450 CYP3A - genetics</subject><subject>Genotype</subject><subject>Humans</subject><subject>Pathologists</subject><subject>Pathology, Molecular</subject><subject>Pharmacists</subject><subject>Pharmacogenetics</subject><subject>Special</subject><issn>1943-7811</issn><issn>1525-1578</issn><issn>1943-7811</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNplkk1z0zAQhg0DQ0vhHzCMjhySYNnyFxcmE0oolCFTyjCcPIq8thVkrZFkINz538hJ20nLSav9eN7dlYLgGQ1nNKTpy81s06Gqfs-iMIpnYToLw_x-cEwLFk-znNIHB_ZR8NjaTRhSxtLoUXAUZ4wWEUuO7_1dfFvFc0a4rsjOTMgSNLptL3VDLkBg14GuuJOo7SsyJ-9RakcW_gbaDvZOCsGauBbI3FoUcu-q0ZCPqEAMihuy4q5Fhc12QhZKaim4IquWm44LbECDk8KSs65X4KFuTxjV0Dg5dL4IlYIGRqF5B8bX6xumtM5OyJvBifZ_5lc038eZlgaH_rrPC9x6_VsVI-Sw_wk5HQz24HU-ex-47W6iAz52I3_c4AqMRc2V_AMVuWzB8N7PuYvcTf-g8ZeCqoE1t_AkeFhzZeHp1XkSfHl7erl4Nz3_tDxbzM-nPc0jN60zgDXk67RIY6ipYEUUM6jXwArKoqIAqDOeFAmLqX9fxqtCFEVS1yLLBI95Fp8Er_fcflh3UAm_YcNV2RvZcbMtkcvydkTLtmzwZ0nDJE3yNPeEF1cEgz8GsK7spBWgFNeAgy2jPE4i_7vSUez5odiNyvXni_8BswjquA</recordid><startdate>202309</startdate><enddate>202309</enddate><creator>Pratt, Victoria M</creator><creator>Cavallari, Larisa H</creator><creator>Fulmer, Makenzie L</creator><creator>Gaedigk, Andrea</creator><creator>Hachad, Houda</creator><creator>Ji, Yuan</creator><creator>Kalman, Lisa V</creator><creator>Ly, Reynold C</creator><creator>Moyer, Ann M</creator><creator>Scott, Stuart A</creator><creator>van Schaik, Ron H N</creator><creator>Whirl-Carrillo, Michelle</creator><creator>Weck, Karen E</creator><general>American Society for Investigative Pathology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>202309</creationdate><title>CYP3A4 and CYP3A5 Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, and Pharmacogenomics Knowledgebase</title><author>Pratt, Victoria M ; Cavallari, Larisa H ; Fulmer, Makenzie L ; Gaedigk, Andrea ; Hachad, Houda ; Ji, Yuan ; Kalman, Lisa V ; Ly, Reynold C ; Moyer, Ann M ; Scott, Stuart A ; van Schaik, Ron H N ; Whirl-Carrillo, Michelle ; Weck, Karen E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p182t-f7eebe8b6963ef1c49234efbe4914299eef7a5954314194ad9c995ffc77ca3a73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Consensus</topic><topic>Cytochrome P-450 CYP3A - genetics</topic><topic>Genotype</topic><topic>Humans</topic><topic>Pathologists</topic><topic>Pathology, Molecular</topic><topic>Pharmacists</topic><topic>Pharmacogenetics</topic><topic>Special</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pratt, Victoria M</creatorcontrib><creatorcontrib>Cavallari, Larisa H</creatorcontrib><creatorcontrib>Fulmer, Makenzie L</creatorcontrib><creatorcontrib>Gaedigk, Andrea</creatorcontrib><creatorcontrib>Hachad, Houda</creatorcontrib><creatorcontrib>Ji, Yuan</creatorcontrib><creatorcontrib>Kalman, Lisa V</creatorcontrib><creatorcontrib>Ly, Reynold C</creatorcontrib><creatorcontrib>Moyer, Ann M</creatorcontrib><creatorcontrib>Scott, Stuart A</creatorcontrib><creatorcontrib>van Schaik, Ron H N</creatorcontrib><creatorcontrib>Whirl-Carrillo, Michelle</creatorcontrib><creatorcontrib>Weck, Karen E</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of molecular diagnostics : JMD</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pratt, Victoria M</au><au>Cavallari, Larisa H</au><au>Fulmer, Makenzie L</au><au>Gaedigk, Andrea</au><au>Hachad, Houda</au><au>Ji, Yuan</au><au>Kalman, Lisa V</au><au>Ly, Reynold C</au><au>Moyer, Ann M</au><au>Scott, Stuart A</au><au>van Schaik, Ron H N</au><au>Whirl-Carrillo, Michelle</au><au>Weck, Karen E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CYP3A4 and CYP3A5 Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, and Pharmacogenomics Knowledgebase</atitle><jtitle>The Journal of molecular diagnostics : JMD</jtitle><addtitle>J Mol Diagn</addtitle><date>2023-09</date><risdate>2023</risdate><volume>25</volume><issue>9</issue><spage>619</spage><epage>629</epage><pages>619-629</pages><issn>1943-7811</issn><issn>1525-1578</issn><eissn>1943-7811</eissn><abstract>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 panel of variant alleles (tier 1) and an extended panel 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 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 gene/allele testing across clinical laboratories. This document will focus on clinical CYP3A4 and CYP3A5 PGx testing that may be applied to all CYP3A4- and CYP3A5-related medications. These recommendations are not to be interpreted as prescriptive but to provide a reference guide.</abstract><cop>United States</cop><pub>American Society for Investigative Pathology</pub><pmid>37419245</pmid><doi>10.1016/j.jmoldx.2023.06.008</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1943-7811 |
ispartof | The Journal of molecular diagnostics : JMD, 2023-09, Vol.25 (9), p.619-629 |
issn | 1943-7811 1525-1578 1943-7811 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10565868 |
source | MEDLINE; Access via ScienceDirect (Elsevier); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Consensus Cytochrome P-450 CYP3A - genetics Genotype Humans Pathologists Pathology, Molecular Pharmacists Pharmacogenetics Special |
title | CYP3A4 and CYP3A5 Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, and Pharmacogenomics Knowledgebase |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-22T03%3A58%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=CYP3A4%20and%20CYP3A5%20Genotyping%20Recommendations:%20A%20Joint%20Consensus%20Recommendation%20of%20the%20Association%20for%20Molecular%20Pathology,%20Clinical%20Pharmacogenetics%20Implementation%20Consortium,%20College%20of%20American%20Pathologists,%20Dutch%20Pharmacogenetics%20Working%20Group%20of%20the%20Royal%20Dutch%20Pharmacists%20Association,%20European%20Society%20for%20Pharmacogenomics%20and%20Personalized%20Therapy,%20and%20Pharmacogenomics%20Knowledgebase&rft.jtitle=The%20Journal%20of%20molecular%20diagnostics%20:%20JMD&rft.au=Pratt,%20Victoria%20M&rft.date=2023-09&rft.volume=25&rft.issue=9&rft.spage=619&rft.epage=629&rft.pages=619-629&rft.issn=1943-7811&rft.eissn=1943-7811&rft_id=info:doi/10.1016/j.jmoldx.2023.06.008&rft_dat=%3Cproquest_pubme%3E2835274167%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2835274167&rft_id=info:pmid/37419245&rfr_iscdi=true |