A population‐based study of the drug interaction between clopidogrel and angiotensin converting enzyme inhibitors

Aims Clopidogrel and angiotensin converting enzyme (ACE) inhibitors are commonly co‐prescribed drugs. Clopidogrel inhibits carboxylesterase 1 (CES1), the enzyme responsible for converting prodrug ACE inhibitors (such as ramipril and perindopril) to their active metabolites. The clinical implications...

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Veröffentlicht in:British journal of clinical pharmacology 2015-10, Vol.80 (4), p.662-669
Hauptverfasser: Cressman, Alex M., Macdonald, Erin M., Fernandes, Kimberly A., Gomes, Tara, Paterson, J. Michael, Mamdani, Muhammad M., Juurlink, David N.
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container_issue 4
container_start_page 662
container_title British journal of clinical pharmacology
container_volume 80
creator Cressman, Alex M.
Macdonald, Erin M.
Fernandes, Kimberly A.
Gomes, Tara
Paterson, J. Michael
Mamdani, Muhammad M.
Juurlink, David N.
description Aims Clopidogrel and angiotensin converting enzyme (ACE) inhibitors are commonly co‐prescribed drugs. Clopidogrel inhibits carboxylesterase 1 (CES1), the enzyme responsible for converting prodrug ACE inhibitors (such as ramipril and perindopril) to their active metabolites. The clinical implications of this potential drug interaction are unknown. The clinical consequences of the potential drug interaction between clopidogrel and prodrug ACE inhibitors were examined. Methods We conducted a nested case–control study of Ontarians aged 66 years and older treated with clopidogrel between September 1 2003 and March 31 2013 following acute myocardial infarction. Cases were subjects who died or were hospitalized for reinfarction or heart failure in the subsequent year, and each was matched with up to four controls. The primary outcome was a composite of reinfarction, heart failure or death. The primary analysis examined whether use of the prodrug ACE inhibitors ramipril or perindopril was more common among cases than use of lisinopril, an active ACE inhibitor. Results Among 45 918 patients treated with clopidogrel following myocardial infarction, we identified 4203 cases and 14 964 controls. After adjustment, we found no association between the composite outcome and use of perindopril (adjusted odds ratio (aOR) 0.94, 95% confidence interval (CI) 0.76, 1.16) or ramipril (aOR 0.97, 95% CI 0.80, 1.18), relative to lisinopril. Secondary analyses of each element of the composite outcome yielded similar findings. Conclusions Following myocardial infarction, use of clopidogrel with ACE inhibitors activated by CES1 is not associated with an increased risk of adverse cardiovascular outcomes relative to lisinopril. These findings suggest that the recently described drug interaction between clopidogrel and prodrug ACE inhibitors is of little clinical relevance.
doi_str_mv 10.1111/bcp.12682
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Michael ; Mamdani, Muhammad M. ; Juurlink, David N.</creator><creatorcontrib>Cressman, Alex M. ; Macdonald, Erin M. ; Fernandes, Kimberly A. ; Gomes, Tara ; Paterson, J. Michael ; Mamdani, Muhammad M. ; Juurlink, David N. ; Canadian Drug Safety Effectiveness Research Network (CDSERN)</creatorcontrib><description>Aims Clopidogrel and angiotensin converting enzyme (ACE) inhibitors are commonly co‐prescribed drugs. Clopidogrel inhibits carboxylesterase 1 (CES1), the enzyme responsible for converting prodrug ACE inhibitors (such as ramipril and perindopril) to their active metabolites. The clinical implications of this potential drug interaction are unknown. The clinical consequences of the potential drug interaction between clopidogrel and prodrug ACE inhibitors were examined. Methods We conducted a nested case–control study of Ontarians aged 66 years and older treated with clopidogrel between September 1 2003 and March 31 2013 following acute myocardial infarction. Cases were subjects who died or were hospitalized for reinfarction or heart failure in the subsequent year, and each was matched with up to four controls. The primary outcome was a composite of reinfarction, heart failure or death. The primary analysis examined whether use of the prodrug ACE inhibitors ramipril or perindopril was more common among cases than use of lisinopril, an active ACE inhibitor. Results Among 45 918 patients treated with clopidogrel following myocardial infarction, we identified 4203 cases and 14 964 controls. After adjustment, we found no association between the composite outcome and use of perindopril (adjusted odds ratio (aOR) 0.94, 95% confidence interval (CI) 0.76, 1.16) or ramipril (aOR 0.97, 95% CI 0.80, 1.18), relative to lisinopril. Secondary analyses of each element of the composite outcome yielded similar findings. Conclusions Following myocardial infarction, use of clopidogrel with ACE inhibitors activated by CES1 is not associated with an increased risk of adverse cardiovascular outcomes relative to lisinopril. These findings suggest that the recently described drug interaction between clopidogrel and prodrug ACE inhibitors is of little clinical relevance.</description><identifier>ISSN: 0306-5251</identifier><identifier>EISSN: 1365-2125</identifier><identifier>DOI: 10.1111/bcp.12682</identifier><identifier>PMID: 25980448</identifier><language>eng</language><publisher>England: John Wiley &amp; Sons, Ltd</publisher><subject>Aged ; angiotensin converting enzyme inhibitors ; Angiotensin-Converting Enzyme Inhibitors - pharmacology ; Angiotensin-Converting Enzyme Inhibitors - therapeutic use ; Case-Control Studies ; clopidogrel ; congestive heart failure ; Databases, Factual ; Drug Interactions ; Drug Therapy, Combination ; Female ; Heart Failure ; Humans ; Lisinopril - pharmacology ; Lisinopril - therapeutic use ; Male ; mortality ; myocardial infarction ; Myocardial Infarction - drug therapy ; Perindopril - pharmacology ; Perindopril - therapeutic use ; Pharmacoepidemiology ; Platelet Aggregation Inhibitors - pharmacology ; Ramipril - pharmacology ; Ramipril - therapeutic use ; Recurrence ; Ticlopidine - analogs &amp; derivatives ; Ticlopidine - pharmacology ; Ticlopidine - therapeutic use ; Treatment Outcome</subject><ispartof>British journal of clinical pharmacology, 2015-10, Vol.80 (4), p.662-669</ispartof><rights>2015 The Authors. British Journal of Clinical Pharmacology published by John Wiley &amp; Sons Ltd on behalf of The British Pharmacological Society.</rights><rights>2015 The British Pharmacological Society 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4852-2969268b40cdb5b0c70e0f1755e2288c6e57c565929bd4827ca9d2e1b315c7da3</citedby><cites>FETCH-LOGICAL-c4852-2969268b40cdb5b0c70e0f1755e2288c6e57c565929bd4827ca9d2e1b315c7da3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fbcp.12682$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fbcp.12682$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,777,781,882,1412,1428,27905,27906,45555,45556,46390,46814</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25980448$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cressman, Alex M.</creatorcontrib><creatorcontrib>Macdonald, Erin M.</creatorcontrib><creatorcontrib>Fernandes, Kimberly A.</creatorcontrib><creatorcontrib>Gomes, Tara</creatorcontrib><creatorcontrib>Paterson, J. Michael</creatorcontrib><creatorcontrib>Mamdani, Muhammad M.</creatorcontrib><creatorcontrib>Juurlink, David N.</creatorcontrib><creatorcontrib>Canadian Drug Safety Effectiveness Research Network (CDSERN)</creatorcontrib><title>A population‐based study of the drug interaction between clopidogrel and angiotensin converting enzyme inhibitors</title><title>British journal of clinical pharmacology</title><addtitle>Br J Clin Pharmacol</addtitle><description>Aims Clopidogrel and angiotensin converting enzyme (ACE) inhibitors are commonly co‐prescribed drugs. Clopidogrel inhibits carboxylesterase 1 (CES1), the enzyme responsible for converting prodrug ACE inhibitors (such as ramipril and perindopril) to their active metabolites. The clinical implications of this potential drug interaction are unknown. The clinical consequences of the potential drug interaction between clopidogrel and prodrug ACE inhibitors were examined. Methods We conducted a nested case–control study of Ontarians aged 66 years and older treated with clopidogrel between September 1 2003 and March 31 2013 following acute myocardial infarction. Cases were subjects who died or were hospitalized for reinfarction or heart failure in the subsequent year, and each was matched with up to four controls. The primary outcome was a composite of reinfarction, heart failure or death. The primary analysis examined whether use of the prodrug ACE inhibitors ramipril or perindopril was more common among cases than use of lisinopril, an active ACE inhibitor. Results Among 45 918 patients treated with clopidogrel following myocardial infarction, we identified 4203 cases and 14 964 controls. After adjustment, we found no association between the composite outcome and use of perindopril (adjusted odds ratio (aOR) 0.94, 95% confidence interval (CI) 0.76, 1.16) or ramipril (aOR 0.97, 95% CI 0.80, 1.18), relative to lisinopril. Secondary analyses of each element of the composite outcome yielded similar findings. Conclusions Following myocardial infarction, use of clopidogrel with ACE inhibitors activated by CES1 is not associated with an increased risk of adverse cardiovascular outcomes relative to lisinopril. These findings suggest that the recently described drug interaction between clopidogrel and prodrug ACE inhibitors is of little clinical relevance.</description><subject>Aged</subject><subject>angiotensin converting enzyme inhibitors</subject><subject>Angiotensin-Converting Enzyme Inhibitors - pharmacology</subject><subject>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</subject><subject>Case-Control Studies</subject><subject>clopidogrel</subject><subject>congestive heart failure</subject><subject>Databases, Factual</subject><subject>Drug Interactions</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Heart Failure</subject><subject>Humans</subject><subject>Lisinopril - pharmacology</subject><subject>Lisinopril - therapeutic use</subject><subject>Male</subject><subject>mortality</subject><subject>myocardial infarction</subject><subject>Myocardial Infarction - drug therapy</subject><subject>Perindopril - pharmacology</subject><subject>Perindopril - therapeutic use</subject><subject>Pharmacoepidemiology</subject><subject>Platelet Aggregation Inhibitors - pharmacology</subject><subject>Ramipril - pharmacology</subject><subject>Ramipril - therapeutic use</subject><subject>Recurrence</subject><subject>Ticlopidine - analogs &amp; derivatives</subject><subject>Ticlopidine - pharmacology</subject><subject>Ticlopidine - therapeutic use</subject><subject>Treatment Outcome</subject><issn>0306-5251</issn><issn>1365-2125</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp1kUtOHDEQhq0IFCYki1wAeQmLBtvd7scGCUYQkJDIIllbftT0GPXYHdsNmqxyBM7ISeLJAAoLLJW8qE9fVelH6CslxzS_E6XHY8rqln1AM1rWvGCU8R00IyWpC8443UOfYrwjhJa05h_RHuNdS6qqnaF4hkc_ToNM1runP49KRjA4psmssV_gtARswtRj6xIEqTcUVpAeABzWgx-t8X2AAUtncvXWJ3DR5p539xCSdT0G93u9gmxYWmWTD_Ez2l3IIcKX538f_by8-DG_Km5uv13Pz24KXbWcFayru3yUqog2iiuiGwJkQRvOgbG21TXwRvOad6xTpmpZo2VnGFBVUq4bI8t9dLr1jpNagdHgUpCDGINdybAWXlrxtuPsUvT-XlS8qxrCsuDwWRD8rwliEisbNQyDdOCnKGhDm81gUmf0aIvq4GMMsHgdQ4nYhCRySOJfSJk9-H-vV_IllQycbIEHO8D6fZM4n3_fKv8CicOf9g</recordid><startdate>201510</startdate><enddate>201510</enddate><creator>Cressman, Alex M.</creator><creator>Macdonald, Erin M.</creator><creator>Fernandes, Kimberly A.</creator><creator>Gomes, Tara</creator><creator>Paterson, J. Michael</creator><creator>Mamdani, Muhammad M.</creator><creator>Juurlink, David N.</creator><general>John Wiley &amp; Sons, Ltd</general><scope>24P</scope><scope>WIN</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>201510</creationdate><title>A population‐based study of the drug interaction between clopidogrel and angiotensin converting enzyme inhibitors</title><author>Cressman, Alex M. ; Macdonald, Erin M. ; Fernandes, Kimberly A. ; Gomes, Tara ; Paterson, J. Michael ; Mamdani, Muhammad M. ; Juurlink, David N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4852-2969268b40cdb5b0c70e0f1755e2288c6e57c565929bd4827ca9d2e1b315c7da3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aged</topic><topic>angiotensin converting enzyme inhibitors</topic><topic>Angiotensin-Converting Enzyme Inhibitors - pharmacology</topic><topic>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</topic><topic>Case-Control Studies</topic><topic>clopidogrel</topic><topic>congestive heart failure</topic><topic>Databases, Factual</topic><topic>Drug Interactions</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Heart Failure</topic><topic>Humans</topic><topic>Lisinopril - pharmacology</topic><topic>Lisinopril - therapeutic use</topic><topic>Male</topic><topic>mortality</topic><topic>myocardial infarction</topic><topic>Myocardial Infarction - drug therapy</topic><topic>Perindopril - pharmacology</topic><topic>Perindopril - therapeutic use</topic><topic>Pharmacoepidemiology</topic><topic>Platelet Aggregation Inhibitors - pharmacology</topic><topic>Ramipril - pharmacology</topic><topic>Ramipril - therapeutic use</topic><topic>Recurrence</topic><topic>Ticlopidine - analogs &amp; derivatives</topic><topic>Ticlopidine - pharmacology</topic><topic>Ticlopidine - therapeutic use</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cressman, Alex M.</creatorcontrib><creatorcontrib>Macdonald, Erin M.</creatorcontrib><creatorcontrib>Fernandes, Kimberly A.</creatorcontrib><creatorcontrib>Gomes, Tara</creatorcontrib><creatorcontrib>Paterson, J. Michael</creatorcontrib><creatorcontrib>Mamdani, Muhammad M.</creatorcontrib><creatorcontrib>Juurlink, David N.</creatorcontrib><creatorcontrib>Canadian Drug Safety Effectiveness Research Network (CDSERN)</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of clinical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cressman, Alex M.</au><au>Macdonald, Erin M.</au><au>Fernandes, Kimberly A.</au><au>Gomes, Tara</au><au>Paterson, J. Michael</au><au>Mamdani, Muhammad M.</au><au>Juurlink, David N.</au><aucorp>Canadian Drug Safety Effectiveness Research Network (CDSERN)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A population‐based study of the drug interaction between clopidogrel and angiotensin converting enzyme inhibitors</atitle><jtitle>British journal of clinical pharmacology</jtitle><addtitle>Br J Clin Pharmacol</addtitle><date>2015-10</date><risdate>2015</risdate><volume>80</volume><issue>4</issue><spage>662</spage><epage>669</epage><pages>662-669</pages><issn>0306-5251</issn><eissn>1365-2125</eissn><abstract>Aims Clopidogrel and angiotensin converting enzyme (ACE) inhibitors are commonly co‐prescribed drugs. Clopidogrel inhibits carboxylesterase 1 (CES1), the enzyme responsible for converting prodrug ACE inhibitors (such as ramipril and perindopril) to their active metabolites. The clinical implications of this potential drug interaction are unknown. The clinical consequences of the potential drug interaction between clopidogrel and prodrug ACE inhibitors were examined. Methods We conducted a nested case–control study of Ontarians aged 66 years and older treated with clopidogrel between September 1 2003 and March 31 2013 following acute myocardial infarction. Cases were subjects who died or were hospitalized for reinfarction or heart failure in the subsequent year, and each was matched with up to four controls. The primary outcome was a composite of reinfarction, heart failure or death. The primary analysis examined whether use of the prodrug ACE inhibitors ramipril or perindopril was more common among cases than use of lisinopril, an active ACE inhibitor. Results Among 45 918 patients treated with clopidogrel following myocardial infarction, we identified 4203 cases and 14 964 controls. After adjustment, we found no association between the composite outcome and use of perindopril (adjusted odds ratio (aOR) 0.94, 95% confidence interval (CI) 0.76, 1.16) or ramipril (aOR 0.97, 95% CI 0.80, 1.18), relative to lisinopril. Secondary analyses of each element of the composite outcome yielded similar findings. Conclusions Following myocardial infarction, use of clopidogrel with ACE inhibitors activated by CES1 is not associated with an increased risk of adverse cardiovascular outcomes relative to lisinopril. These findings suggest that the recently described drug interaction between clopidogrel and prodrug ACE inhibitors is of little clinical relevance.</abstract><cop>England</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>25980448</pmid><doi>10.1111/bcp.12682</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
angiotensin converting enzyme inhibitors
Angiotensin-Converting Enzyme Inhibitors - pharmacology
Angiotensin-Converting Enzyme Inhibitors - therapeutic use
Case-Control Studies
clopidogrel
congestive heart failure
Databases, Factual
Drug Interactions
Drug Therapy, Combination
Female
Heart Failure
Humans
Lisinopril - pharmacology
Lisinopril - therapeutic use
Male
mortality
myocardial infarction
Myocardial Infarction - drug therapy
Perindopril - pharmacology
Perindopril - therapeutic use
Pharmacoepidemiology
Platelet Aggregation Inhibitors - pharmacology
Ramipril - pharmacology
Ramipril - therapeutic use
Recurrence
Ticlopidine - analogs & derivatives
Ticlopidine - pharmacology
Ticlopidine - therapeutic use
Treatment Outcome
title A population‐based study of the drug interaction between clopidogrel and angiotensin converting enzyme inhibitors
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