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Impact of CYP2C19 Genotype on Efficacy and Safety of Clopidogrel-based Antiplatelet Therapy in Stroke or Transient Ischemic Attack Patients: An Updated Systematic Review and Meta-analysis of Non-East Asian Studies
Purpose Inconclusive and limited results have been reported on the clinical utility of CYP2C19 genotyping in stroke/TIA patients of non-East Asian ancestries. We herein performed an updated systematic review and meta-analysis to quantitatively estimate the association of CYP2C19 loss-of function (LO...
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Published in: | Cardiovascular drugs and therapy 2024-12, Vol.38 (6), p.1397-1407 |
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creator | Cargnin, Sarah Ferrari, Federica Terrazzino, Salvatore |
description | Purpose
Inconclusive and limited results have been reported on the clinical utility of CYP2C19 genotyping in stroke/TIA patients of non-East Asian ancestries. We herein performed an updated systematic review and meta-analysis to quantitatively estimate the association of CYP2C19 loss-of function (LOF) status with efficacy and safety of clopidogrel-based antiplatelet therapy in non-East Asian patients affected by stroke or TIA.
Methods
A comprehensive search was performed up to July 2023 using PubMed, Web of Knowledge, and Cochrane Library databases. The clinical outcomes investigated were stroke, composite vascular events and bleeding. Pooled estimates were calculated as risk ratios (RR) with 95% CI using the Mantel– Haenszel random-effects model. The quality of evidence was assessed using the GRADEpro tool.
Results
A total number of 1673 stroke/TIA patients from 8 non-East Asian studies, published between 2014 and 2022, were included in the systematic review. Clopidogrel-treated carriers of CYP2C19 LOF alleles were found at increased risk of stroke compared to non-carriers (RR: 1.68, 95%CI: 1.04–2.71, P = 0.03). However, no significant association was observed with the risk of composite vascular events (RR: 1.15, 95%CI: 0.58–2.28, P = 0.69) or bleeding (RR: 0.84, 95%CI: 0.38–1.86, P = 0.67). Similarly, European ancestry patients carrying CYP2C19 LOF alleles displayed a higher risk of stroke (RR: 2.69 (1.11–6.51, P = 0.03), but not of composite vascular events or bleeding.
Conclusion
The present updated meta-analysis provides moderate quality evidence of association between CYP2C19 LOF alleles and an increased risk of stroke in non-East Asian patients with stroke/TIA after receiving clopidogrel therapy. Further large pharmacogenetic studies are still warranted to corroborate these findings. |
doi_str_mv | 10.1007/s10557-023-07534-0 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11680632</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2896810899</sourcerecordid><originalsourceid>FETCH-LOGICAL-c426t-634f2023ad9d080e0a07e455a509bfb50bcbba1562dc0abe0a3d6ffdab5b828f3</originalsourceid><addsrcrecordid>eNp9kstu1DAUhiMEokPhBVggS2zYBHzJxWGDRqOhjFSgotMFK-vEOZlxm8TB9hTlQXkfPDOlXBasLPn_zn8u-pPkOaOvGaXlG89onpcp5SKlZS6ylD5IZiwvRVryjD1MZrTiNBWcFifJE--vaSyqKvk4ORGSCilZNUt-rPoRdCC2JYuvF3zBKnKGgw3TiMQOZNm2RoOeCAwNuYQWw3RAOzuaxm4cdmkNHhsyH4IZOwjYYSDrLToYJ2IGchmcvYlWjqwdDN7gEMjK6y32RpN5CKBvyAWE_b9_G13I1dhEl9hs8gH7qGjyBW8Nfj-M8BEDpDBAN3nj95N8skO6BB_I3BvYt9s1Bv3T5FELncdnd-9pcvV-uV58SM8_n60W8_NUZ7wIaSGylsfzQVM1VFKkQEvM8hxyWtVtndNa1zWwvOCNplBHXTRF2zZQ57XkshWnybuj77ire2x03MJBp0ZnenCTsmDU38pgtmpjbxVjhaSF4NHh1Z2Ds9926IPqjdfYdTCg3XnFZVVIRmVVRfTlP-i13bl4C68Ey6pCSFGwSPEjpZ313mF7Pw2jah8bdYyNinurQ2wUjUUv_tzjvuRXTiIgjoCP0rBB97v3f2x_AjWN0Z4</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3149638361</pqid></control><display><type>article</type><title>Impact of CYP2C19 Genotype on Efficacy and Safety of Clopidogrel-based Antiplatelet Therapy in Stroke or Transient Ischemic Attack Patients: An Updated Systematic Review and Meta-analysis of Non-East Asian Studies</title><source>Springer Nature</source><creator>Cargnin, Sarah ; Ferrari, Federica ; Terrazzino, Salvatore</creator><creatorcontrib>Cargnin, Sarah ; Ferrari, Federica ; Terrazzino, Salvatore</creatorcontrib><description>Purpose
Inconclusive and limited results have been reported on the clinical utility of CYP2C19 genotyping in stroke/TIA patients of non-East Asian ancestries. We herein performed an updated systematic review and meta-analysis to quantitatively estimate the association of CYP2C19 loss-of function (LOF) status with efficacy and safety of clopidogrel-based antiplatelet therapy in non-East Asian patients affected by stroke or TIA.
Methods
A comprehensive search was performed up to July 2023 using PubMed, Web of Knowledge, and Cochrane Library databases. The clinical outcomes investigated were stroke, composite vascular events and bleeding. Pooled estimates were calculated as risk ratios (RR) with 95% CI using the Mantel– Haenszel random-effects model. The quality of evidence was assessed using the GRADEpro tool.
Results
A total number of 1673 stroke/TIA patients from 8 non-East Asian studies, published between 2014 and 2022, were included in the systematic review. Clopidogrel-treated carriers of CYP2C19 LOF alleles were found at increased risk of stroke compared to non-carriers (RR: 1.68, 95%CI: 1.04–2.71, P = 0.03). However, no significant association was observed with the risk of composite vascular events (RR: 1.15, 95%CI: 0.58–2.28, P = 0.69) or bleeding (RR: 0.84, 95%CI: 0.38–1.86, P = 0.67). Similarly, European ancestry patients carrying CYP2C19 LOF alleles displayed a higher risk of stroke (RR: 2.69 (1.11–6.51, P = 0.03), but not of composite vascular events or bleeding.
Conclusion
The present updated meta-analysis provides moderate quality evidence of association between CYP2C19 LOF alleles and an increased risk of stroke in non-East Asian patients with stroke/TIA after receiving clopidogrel therapy. Further large pharmacogenetic studies are still warranted to corroborate these findings.</description><identifier>ISSN: 0920-3206</identifier><identifier>ISSN: 1573-7241</identifier><identifier>EISSN: 1573-7241</identifier><identifier>DOI: 10.1007/s10557-023-07534-0</identifier><identifier>PMID: 38038819</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Aged ; Alleles ; Antiplatelet therapy ; Asian People - genetics ; Bleeding ; Cardiology ; Clopidogrel ; Clopidogrel - adverse effects ; Clopidogrel - therapeutic use ; Cytochrome P-450 CYP2C19 - genetics ; East Asian studies ; Effectiveness ; Female ; Genotype ; Genotypes ; Genotyping ; Hemorrhage - chemically induced ; Hemorrhage - genetics ; Humans ; Ischemia ; Ischemic Attack, Transient - drug therapy ; Ischemic Attack, Transient - genetics ; Male ; Medicine ; Medicine & Public Health ; Meta-analysis ; Middle Aged ; Original ; Original Article ; Pharmacogenomic Variants ; Platelet Aggregation Inhibitors - adverse effects ; Platelet Aggregation Inhibitors - therapeutic use ; Risk Assessment ; Risk Factors ; Stroke ; Stroke - drug therapy ; Stroke - genetics ; Systematic review ; Therapy ; Transient ischemic attack ; Treatment Outcome</subject><ispartof>Cardiovascular drugs and therapy, 2024-12, Vol.38 (6), p.1397-1407</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>Copyright Springer Nature B.V. Dec 2024</rights><rights>The Author(s) 2023 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c426t-634f2023ad9d080e0a07e455a509bfb50bcbba1562dc0abe0a3d6ffdab5b828f3</cites><orcidid>0000-0002-4909-1121</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38038819$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cargnin, Sarah</creatorcontrib><creatorcontrib>Ferrari, Federica</creatorcontrib><creatorcontrib>Terrazzino, Salvatore</creatorcontrib><title>Impact of CYP2C19 Genotype on Efficacy and Safety of Clopidogrel-based Antiplatelet Therapy in Stroke or Transient Ischemic Attack Patients: An Updated Systematic Review and Meta-analysis of Non-East Asian Studies</title><title>Cardiovascular drugs and therapy</title><addtitle>Cardiovasc Drugs Ther</addtitle><addtitle>Cardiovasc Drugs Ther</addtitle><description>Purpose
Inconclusive and limited results have been reported on the clinical utility of CYP2C19 genotyping in stroke/TIA patients of non-East Asian ancestries. We herein performed an updated systematic review and meta-analysis to quantitatively estimate the association of CYP2C19 loss-of function (LOF) status with efficacy and safety of clopidogrel-based antiplatelet therapy in non-East Asian patients affected by stroke or TIA.
Methods
A comprehensive search was performed up to July 2023 using PubMed, Web of Knowledge, and Cochrane Library databases. The clinical outcomes investigated were stroke, composite vascular events and bleeding. Pooled estimates were calculated as risk ratios (RR) with 95% CI using the Mantel– Haenszel random-effects model. The quality of evidence was assessed using the GRADEpro tool.
Results
A total number of 1673 stroke/TIA patients from 8 non-East Asian studies, published between 2014 and 2022, were included in the systematic review. Clopidogrel-treated carriers of CYP2C19 LOF alleles were found at increased risk of stroke compared to non-carriers (RR: 1.68, 95%CI: 1.04–2.71, P = 0.03). However, no significant association was observed with the risk of composite vascular events (RR: 1.15, 95%CI: 0.58–2.28, P = 0.69) or bleeding (RR: 0.84, 95%CI: 0.38–1.86, P = 0.67). Similarly, European ancestry patients carrying CYP2C19 LOF alleles displayed a higher risk of stroke (RR: 2.69 (1.11–6.51, P = 0.03), but not of composite vascular events or bleeding.
Conclusion
The present updated meta-analysis provides moderate quality evidence of association between CYP2C19 LOF alleles and an increased risk of stroke in non-East Asian patients with stroke/TIA after receiving clopidogrel therapy. Further large pharmacogenetic studies are still warranted to corroborate these findings.</description><subject>Aged</subject><subject>Alleles</subject><subject>Antiplatelet therapy</subject><subject>Asian People - genetics</subject><subject>Bleeding</subject><subject>Cardiology</subject><subject>Clopidogrel</subject><subject>Clopidogrel - adverse effects</subject><subject>Clopidogrel - therapeutic use</subject><subject>Cytochrome P-450 CYP2C19 - genetics</subject><subject>East Asian studies</subject><subject>Effectiveness</subject><subject>Female</subject><subject>Genotype</subject><subject>Genotypes</subject><subject>Genotyping</subject><subject>Hemorrhage - chemically induced</subject><subject>Hemorrhage - genetics</subject><subject>Humans</subject><subject>Ischemia</subject><subject>Ischemic Attack, Transient - drug therapy</subject><subject>Ischemic Attack, Transient - genetics</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Meta-analysis</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Original Article</subject><subject>Pharmacogenomic Variants</subject><subject>Platelet Aggregation Inhibitors - adverse effects</subject><subject>Platelet Aggregation Inhibitors - therapeutic use</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>Stroke</subject><subject>Stroke - drug therapy</subject><subject>Stroke - genetics</subject><subject>Systematic review</subject><subject>Therapy</subject><subject>Transient ischemic attack</subject><subject>Treatment Outcome</subject><issn>0920-3206</issn><issn>1573-7241</issn><issn>1573-7241</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kstu1DAUhiMEokPhBVggS2zYBHzJxWGDRqOhjFSgotMFK-vEOZlxm8TB9hTlQXkfPDOlXBasLPn_zn8u-pPkOaOvGaXlG89onpcp5SKlZS6ylD5IZiwvRVryjD1MZrTiNBWcFifJE--vaSyqKvk4ORGSCilZNUt-rPoRdCC2JYuvF3zBKnKGgw3TiMQOZNm2RoOeCAwNuYQWw3RAOzuaxm4cdmkNHhsyH4IZOwjYYSDrLToYJ2IGchmcvYlWjqwdDN7gEMjK6y32RpN5CKBvyAWE_b9_G13I1dhEl9hs8gH7qGjyBW8Nfj-M8BEDpDBAN3nj95N8skO6BB_I3BvYt9s1Bv3T5FELncdnd-9pcvV-uV58SM8_n60W8_NUZ7wIaSGylsfzQVM1VFKkQEvM8hxyWtVtndNa1zWwvOCNplBHXTRF2zZQ57XkshWnybuj77ire2x03MJBp0ZnenCTsmDU38pgtmpjbxVjhaSF4NHh1Z2Ds9926IPqjdfYdTCg3XnFZVVIRmVVRfTlP-i13bl4C68Ey6pCSFGwSPEjpZ313mF7Pw2jah8bdYyNinurQ2wUjUUv_tzjvuRXTiIgjoCP0rBB97v3f2x_AjWN0Z4</recordid><startdate>20241201</startdate><enddate>20241201</enddate><creator>Cargnin, Sarah</creator><creator>Ferrari, Federica</creator><creator>Terrazzino, Salvatore</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4909-1121</orcidid></search><sort><creationdate>20241201</creationdate><title>Impact of CYP2C19 Genotype on Efficacy and Safety of Clopidogrel-based Antiplatelet Therapy in Stroke or Transient Ischemic Attack Patients: An Updated Systematic Review and Meta-analysis of Non-East Asian Studies</title><author>Cargnin, Sarah ; Ferrari, Federica ; Terrazzino, Salvatore</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-634f2023ad9d080e0a07e455a509bfb50bcbba1562dc0abe0a3d6ffdab5b828f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aged</topic><topic>Alleles</topic><topic>Antiplatelet therapy</topic><topic>Asian People - genetics</topic><topic>Bleeding</topic><topic>Cardiology</topic><topic>Clopidogrel</topic><topic>Clopidogrel - adverse effects</topic><topic>Clopidogrel - therapeutic use</topic><topic>Cytochrome P-450 CYP2C19 - genetics</topic><topic>East Asian studies</topic><topic>Effectiveness</topic><topic>Female</topic><topic>Genotype</topic><topic>Genotypes</topic><topic>Genotyping</topic><topic>Hemorrhage - chemically induced</topic><topic>Hemorrhage - genetics</topic><topic>Humans</topic><topic>Ischemia</topic><topic>Ischemic Attack, Transient - drug therapy</topic><topic>Ischemic Attack, Transient - genetics</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Meta-analysis</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Original Article</topic><topic>Pharmacogenomic Variants</topic><topic>Platelet Aggregation Inhibitors - adverse effects</topic><topic>Platelet Aggregation Inhibitors - therapeutic use</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>Stroke</topic><topic>Stroke - drug therapy</topic><topic>Stroke - genetics</topic><topic>Systematic review</topic><topic>Therapy</topic><topic>Transient ischemic attack</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cargnin, Sarah</creatorcontrib><creatorcontrib>Ferrari, Federica</creatorcontrib><creatorcontrib>Terrazzino, Salvatore</creatorcontrib><collection>SpringerOpen</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cardiovascular drugs and therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cargnin, Sarah</au><au>Ferrari, Federica</au><au>Terrazzino, Salvatore</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of CYP2C19 Genotype on Efficacy and Safety of Clopidogrel-based Antiplatelet Therapy in Stroke or Transient Ischemic Attack Patients: An Updated Systematic Review and Meta-analysis of Non-East Asian Studies</atitle><jtitle>Cardiovascular drugs and therapy</jtitle><stitle>Cardiovasc Drugs Ther</stitle><addtitle>Cardiovasc Drugs Ther</addtitle><date>2024-12-01</date><risdate>2024</risdate><volume>38</volume><issue>6</issue><spage>1397</spage><epage>1407</epage><pages>1397-1407</pages><issn>0920-3206</issn><issn>1573-7241</issn><eissn>1573-7241</eissn><abstract>Purpose
Inconclusive and limited results have been reported on the clinical utility of CYP2C19 genotyping in stroke/TIA patients of non-East Asian ancestries. We herein performed an updated systematic review and meta-analysis to quantitatively estimate the association of CYP2C19 loss-of function (LOF) status with efficacy and safety of clopidogrel-based antiplatelet therapy in non-East Asian patients affected by stroke or TIA.
Methods
A comprehensive search was performed up to July 2023 using PubMed, Web of Knowledge, and Cochrane Library databases. The clinical outcomes investigated were stroke, composite vascular events and bleeding. Pooled estimates were calculated as risk ratios (RR) with 95% CI using the Mantel– Haenszel random-effects model. The quality of evidence was assessed using the GRADEpro tool.
Results
A total number of 1673 stroke/TIA patients from 8 non-East Asian studies, published between 2014 and 2022, were included in the systematic review. Clopidogrel-treated carriers of CYP2C19 LOF alleles were found at increased risk of stroke compared to non-carriers (RR: 1.68, 95%CI: 1.04–2.71, P = 0.03). However, no significant association was observed with the risk of composite vascular events (RR: 1.15, 95%CI: 0.58–2.28, P = 0.69) or bleeding (RR: 0.84, 95%CI: 0.38–1.86, P = 0.67). Similarly, European ancestry patients carrying CYP2C19 LOF alleles displayed a higher risk of stroke (RR: 2.69 (1.11–6.51, P = 0.03), but not of composite vascular events or bleeding.
Conclusion
The present updated meta-analysis provides moderate quality evidence of association between CYP2C19 LOF alleles and an increased risk of stroke in non-East Asian patients with stroke/TIA after receiving clopidogrel therapy. Further large pharmacogenetic studies are still warranted to corroborate these findings.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>38038819</pmid><doi>10.1007/s10557-023-07534-0</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-4909-1121</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aged Alleles Antiplatelet therapy Asian People - genetics Bleeding Cardiology Clopidogrel Clopidogrel - adverse effects Clopidogrel - therapeutic use Cytochrome P-450 CYP2C19 - genetics East Asian studies Effectiveness Female Genotype Genotypes Genotyping Hemorrhage - chemically induced Hemorrhage - genetics Humans Ischemia Ischemic Attack, Transient - drug therapy Ischemic Attack, Transient - genetics Male Medicine Medicine & Public Health Meta-analysis Middle Aged Original Original Article Pharmacogenomic Variants Platelet Aggregation Inhibitors - adverse effects Platelet Aggregation Inhibitors - therapeutic use Risk Assessment Risk Factors Stroke Stroke - drug therapy Stroke - genetics Systematic review Therapy Transient ischemic attack Treatment Outcome |
title | Impact of CYP2C19 Genotype on Efficacy and Safety of Clopidogrel-based Antiplatelet Therapy in Stroke or Transient Ischemic Attack Patients: An Updated Systematic Review and Meta-analysis of Non-East Asian Studies |
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