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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
Main Authors: Cargnin, Sarah, Ferrari, Federica, Terrazzino, Salvatore
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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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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 &amp; 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 &amp; 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 &amp; 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 &amp; 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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ispartof Cardiovascular drugs and therapy, 2024-12, Vol.38 (6), p.1397-1407
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source Springer Nature
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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