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 |
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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 |
format | Article |
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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 & 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 & 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 & 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 & 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 & 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 & 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 & 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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