Implementing CYP2C19 Pharmacogenetic Testing for Personalized Antiplatelet Therapy: Findings From the QPGx-CARES Initiative

<h3 dir="ltr">Purpose</h3><p dir="ltr">CYP2C19 loss-of-function (LoF) alleles are associated with increased cardiovascular risk in clopidogrel-treated percutaneous coronary intervention (PCI) patients. Despite the guidelines recommendation for newer P2Y12 inhibi...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: Rania Abdel-latif (18295396) (author)
مؤلفون آخرون: Wadha Al Muftah (3466304) (author), Shaban Mohammed (14150130) (author), Toka AlHsson (22963138) (author), Daoud Al-Badriyeh (832403) (author), Radja Badji (14152548) (author), Awad Al-Qahtani (315456) (author), Abdul Rahman Arabi (12506942) (author), Said Ismail (1567891) (author), Moza Al Hail (2511859) (author), Jassim Al Suwaidi (284932) (author)
منشور في: 2025
الموضوعات:
الوسوم: إضافة وسم
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author Rania Abdel-latif (18295396)
author2 Wadha Al Muftah (3466304)
Shaban Mohammed (14150130)
Toka AlHsson (22963138)
Daoud Al-Badriyeh (832403)
Radja Badji (14152548)
Awad Al-Qahtani (315456)
Abdul Rahman Arabi (12506942)
Said Ismail (1567891)
Moza Al Hail (2511859)
Jassim Al Suwaidi (284932)
author2_role author
author
author
author
author
author
author
author
author
author
author_facet Rania Abdel-latif (18295396)
Wadha Al Muftah (3466304)
Shaban Mohammed (14150130)
Toka AlHsson (22963138)
Daoud Al-Badriyeh (832403)
Radja Badji (14152548)
Awad Al-Qahtani (315456)
Abdul Rahman Arabi (12506942)
Said Ismail (1567891)
Moza Al Hail (2511859)
Jassim Al Suwaidi (284932)
author_role author
dc.creator.none.fl_str_mv Rania Abdel-latif (18295396)
Wadha Al Muftah (3466304)
Shaban Mohammed (14150130)
Toka AlHsson (22963138)
Daoud Al-Badriyeh (832403)
Radja Badji (14152548)
Awad Al-Qahtani (315456)
Abdul Rahman Arabi (12506942)
Said Ismail (1567891)
Moza Al Hail (2511859)
Jassim Al Suwaidi (284932)
dc.date.none.fl_str_mv 2025-12-26T09:00:00Z
dc.identifier.none.fl_str_mv 10.1016/j.clinthera.2025.12.003
dc.relation.none.fl_str_mv https://figshare.com/articles/journal_contribution/Implementing_CYP2C19_Pharmacogenetic_Testing_for_Personalized_Antiplatelet_Therapy_Findings_From_the_QPGx-CARES_Initiative/31017433
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Biomedical and clinical sciences
Cardiovascular medicine and haematology
Pharmacology and pharmaceutical sciences
Antiplatelet therapy
Cardiology
CYP2C19
Pharmacogenetics
Point-of-Care
dc.title.none.fl_str_mv Implementing CYP2C19 Pharmacogenetic Testing for Personalized Antiplatelet Therapy: Findings From the QPGx-CARES Initiative
dc.type.none.fl_str_mv Text
Journal contribution
info:eu-repo/semantics/publishedVersion
text
contribution to journal
description <h3 dir="ltr">Purpose</h3><p dir="ltr">CYP2C19 loss-of-function (LoF) alleles are associated with increased cardiovascular risk in clopidogrel-treated percutaneous coronary intervention (PCI) patients. Despite the guidelines recommendation for newer P2Y12 inhibitors, clopidogrel remains widely prescribed. The study the potential impact and feasibility of implementing pharmacogenetics (PGx) testing to guide antiplatelet therapy and develop strategies for its clinical integration to improve patient management. </p><h3 dir="ltr">Methods</h3><p dir="ltr">A pilot study following a prospective cohort design was conducted within the largest community healthcare provider in Qatar using point-of-care (POC) CYP2C19 genotyping in tailoring antiplatelet therapy for PCI patients. Eligible patients underwent CYP2C19 genotyping, and P2Y12 inhibitor prescriptions were adjusted based on genetic results. The study measured antiplatelet prescribing patterns and identified clinically significant gene-drug interactions. </p><h3 dir="ltr">Findings</h3><p dir="ltr">Out of 376 patients tested, 283 patients received PGx-guided recommendations for anti-platelet therapy. Actionable CYP2C19 alleles were detected in 22% of those patients, prompting a change in drug therapy. PGx-guided recommendations were adopted at a rate of 80%, and CYP2C19 genotyping was a significant predictor of antiplatelet therapy adjustments. A sub-analysis of the cost impact revealed an estimated reduction of 300 QR (82.41 $) per patient annually for ACS patients who underwent PCI with stent placement. </p><h3 dir="ltr">Implications</h3><p dir="ltr">This real-world study highlights the feasibility and clinical impact of CYP2C19 genotyping in guiding antiplatelet therapy for ACS and PCI patients, supporting broader PGx testing implementation in routine cardiovascular care. </p><h3 dir="ltr">Trail registration</h3><p dir="ltr">HMC-IRB Registration: IRB-HMC-2021-011, IRB-MoPH Assurance: IRB-A-HMC-2019-0014. ISRCTN registration: ISRCTN15110009, https://www.isrctn.com/ISRCTN15110009.</p><h2 dir="ltr">Other Information</h2><p dir="ltr">Published in: Clinical Therapeutics<br>License: <a href="http://creativecommons.org/licenses/by/4.0/" target="_blank">http://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.1016/j.clinthera.2025.12.003" target="_blank">https://dx.doi.org/10.1016/j.clinthera.2025.12.003</a></p>
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oai_identifier_str oai:figshare.com:article/31017433
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spelling Implementing CYP2C19 Pharmacogenetic Testing for Personalized Antiplatelet Therapy: Findings From the QPGx-CARES InitiativeRania Abdel-latif (18295396)Wadha Al Muftah (3466304)Shaban Mohammed (14150130)Toka AlHsson (22963138)Daoud Al-Badriyeh (832403)Radja Badji (14152548)Awad Al-Qahtani (315456)Abdul Rahman Arabi (12506942)Said Ismail (1567891)Moza Al Hail (2511859)Jassim Al Suwaidi (284932)Biomedical and clinical sciencesCardiovascular medicine and haematologyPharmacology and pharmaceutical sciencesAntiplatelet therapyCardiologyCYP2C19PharmacogeneticsPoint-of-Care<h3 dir="ltr">Purpose</h3><p dir="ltr">CYP2C19 loss-of-function (LoF) alleles are associated with increased cardiovascular risk in clopidogrel-treated percutaneous coronary intervention (PCI) patients. Despite the guidelines recommendation for newer P2Y12 inhibitors, clopidogrel remains widely prescribed. The study the potential impact and feasibility of implementing pharmacogenetics (PGx) testing to guide antiplatelet therapy and develop strategies for its clinical integration to improve patient management. </p><h3 dir="ltr">Methods</h3><p dir="ltr">A pilot study following a prospective cohort design was conducted within the largest community healthcare provider in Qatar using point-of-care (POC) CYP2C19 genotyping in tailoring antiplatelet therapy for PCI patients. Eligible patients underwent CYP2C19 genotyping, and P2Y12 inhibitor prescriptions were adjusted based on genetic results. The study measured antiplatelet prescribing patterns and identified clinically significant gene-drug interactions. </p><h3 dir="ltr">Findings</h3><p dir="ltr">Out of 376 patients tested, 283 patients received PGx-guided recommendations for anti-platelet therapy. Actionable CYP2C19 alleles were detected in 22% of those patients, prompting a change in drug therapy. PGx-guided recommendations were adopted at a rate of 80%, and CYP2C19 genotyping was a significant predictor of antiplatelet therapy adjustments. A sub-analysis of the cost impact revealed an estimated reduction of 300 QR (82.41 $) per patient annually for ACS patients who underwent PCI with stent placement. </p><h3 dir="ltr">Implications</h3><p dir="ltr">This real-world study highlights the feasibility and clinical impact of CYP2C19 genotyping in guiding antiplatelet therapy for ACS and PCI patients, supporting broader PGx testing implementation in routine cardiovascular care. </p><h3 dir="ltr">Trail registration</h3><p dir="ltr">HMC-IRB Registration: IRB-HMC-2021-011, IRB-MoPH Assurance: IRB-A-HMC-2019-0014. ISRCTN registration: ISRCTN15110009, https://www.isrctn.com/ISRCTN15110009.</p><h2 dir="ltr">Other Information</h2><p dir="ltr">Published in: Clinical Therapeutics<br>License: <a href="http://creativecommons.org/licenses/by/4.0/" target="_blank">http://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.1016/j.clinthera.2025.12.003" target="_blank">https://dx.doi.org/10.1016/j.clinthera.2025.12.003</a></p>2025-12-26T09:00:00ZTextJournal contributioninfo:eu-repo/semantics/publishedVersiontextcontribution to journal10.1016/j.clinthera.2025.12.003https://figshare.com/articles/journal_contribution/Implementing_CYP2C19_Pharmacogenetic_Testing_for_Personalized_Antiplatelet_Therapy_Findings_From_the_QPGx-CARES_Initiative/31017433CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/310174332025-12-26T09:00:00Z
spellingShingle Implementing CYP2C19 Pharmacogenetic Testing for Personalized Antiplatelet Therapy: Findings From the QPGx-CARES Initiative
Rania Abdel-latif (18295396)
Biomedical and clinical sciences
Cardiovascular medicine and haematology
Pharmacology and pharmaceutical sciences
Antiplatelet therapy
Cardiology
CYP2C19
Pharmacogenetics
Point-of-Care
status_str publishedVersion
title Implementing CYP2C19 Pharmacogenetic Testing for Personalized Antiplatelet Therapy: Findings From the QPGx-CARES Initiative
title_full Implementing CYP2C19 Pharmacogenetic Testing for Personalized Antiplatelet Therapy: Findings From the QPGx-CARES Initiative
title_fullStr Implementing CYP2C19 Pharmacogenetic Testing for Personalized Antiplatelet Therapy: Findings From the QPGx-CARES Initiative
title_full_unstemmed Implementing CYP2C19 Pharmacogenetic Testing for Personalized Antiplatelet Therapy: Findings From the QPGx-CARES Initiative
title_short Implementing CYP2C19 Pharmacogenetic Testing for Personalized Antiplatelet Therapy: Findings From the QPGx-CARES Initiative
title_sort Implementing CYP2C19 Pharmacogenetic Testing for Personalized Antiplatelet Therapy: Findings From the QPGx-CARES Initiative
topic Biomedical and clinical sciences
Cardiovascular medicine and haematology
Pharmacology and pharmaceutical sciences
Antiplatelet therapy
Cardiology
CYP2C19
Pharmacogenetics
Point-of-Care