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Utility of whole blood impedance aggregometry for the assessment of clopidogrel action using the novel Multiplate® analyzer—comparison with two flow cytometric methods
Abstract Background Non-responsiveness to anti-platelet therapy has been reported and has been linked to the occurrence of adverse events. No standard method to monitor clopidogrel efficacy is available at present. We aimed at comparing the utility of whole blood impedance aggregometry for the asses...
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Published in: | Thrombosis research 2007, Vol.121 (2), p.249-258 |
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description | Abstract Background Non-responsiveness to anti-platelet therapy has been reported and has been linked to the occurrence of adverse events. No standard method to monitor clopidogrel efficacy is available at present. We aimed at comparing the utility of whole blood impedance aggregometry for the assessment of clopidogrel action using the novel Multiplate® analyzer with two flow cytometric methods. Methods Platelet function was determined before and after the initiation of clopidogrel therapy (300 mg loading dose, followed by 75 mg qd) in 40 patients (observational study). Furthermore, 77 patients and 77 referents with and without clopidogrel treatment (75 mg qd) were evaluated (case control study). Platelet function was assessed by Multiplate® ADP and ADP + PG tests, by P-selectin (CD62P) expression, and by vasodilator stimulated phosphoprotein (VASP) phosphorylation status. Results The observational study revealed that platelet reactivity decreased significantly after clopidogrel administration with all 4 methods ( p < 0.001 for each). In the case control study the median values of all 4 tests were significantly higher in the referents without clopidogrel treatment than in the patients on clopidogrel therapy ( p < 0.001 for each). Applying test specific lower reference limits as criterion for the differentiation between responders and non-responders to clopidogrel treatment, 57% of the patients on clopidogrel therapy were classified as non-responders with the Multiplate® ADP test, 38% with the Multiplate® ADP + PG test, 55% with the P-selectin assay, 9% with the PLT VASP/P2Y12 assay. Conclusions The VASP phosphorylation assay appeared to be advantageous for the assessment of clopidogrel action compared to the Multiplate® ADP + PG test, the P-selectin assay, and the Multiplate® ADP test (listed in descending order). However, our method comparison study underscores the critical nature of the dependence of results on the techniques used in specific studies, and it remains to be elucidated which method correlates best with the occurrence of adverse events. |
doi_str_mv | 10.1016/j.thromres.2007.03.022 |
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No standard method to monitor clopidogrel efficacy is available at present. We aimed at comparing the utility of whole blood impedance aggregometry for the assessment of clopidogrel action using the novel Multiplate® analyzer with two flow cytometric methods. Methods Platelet function was determined before and after the initiation of clopidogrel therapy (300 mg loading dose, followed by 75 mg qd) in 40 patients (observational study). Furthermore, 77 patients and 77 referents with and without clopidogrel treatment (75 mg qd) were evaluated (case control study). Platelet function was assessed by Multiplate® ADP and ADP + PG tests, by P-selectin (CD62P) expression, and by vasodilator stimulated phosphoprotein (VASP) phosphorylation status. Results The observational study revealed that platelet reactivity decreased significantly after clopidogrel administration with all 4 methods ( p < 0.001 for each). In the case control study the median values of all 4 tests were significantly higher in the referents without clopidogrel treatment than in the patients on clopidogrel therapy ( p < 0.001 for each). Applying test specific lower reference limits as criterion for the differentiation between responders and non-responders to clopidogrel treatment, 57% of the patients on clopidogrel therapy were classified as non-responders with the Multiplate® ADP test, 38% with the Multiplate® ADP + PG test, 55% with the P-selectin assay, 9% with the PLT VASP/P2Y12 assay. Conclusions The VASP phosphorylation assay appeared to be advantageous for the assessment of clopidogrel action compared to the Multiplate® ADP + PG test, the P-selectin assay, and the Multiplate® ADP test (listed in descending order). However, our method comparison study underscores the critical nature of the dependence of results on the techniques used in specific studies, and it remains to be elucidated which method correlates best with the occurrence of adverse events.</description><identifier>ISSN: 0049-3848</identifier><identifier>EISSN: 1879-2472</identifier><identifier>DOI: 10.1016/j.thromres.2007.03.022</identifier><identifier>PMID: 17482663</identifier><identifier>CODEN: THBRAA</identifier><language>eng</language><publisher>New York, NY: Elsevier Ltd</publisher><subject>Aged ; Aged, 80 and over ; Aggregometry ; Biological and medical sciences ; Blood and lymphatic vessels ; Brain ; Cardiology. Vascular system ; Cardiovascular disease ; Case-Control Studies ; Clopidogrel ; Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous ; Drug Resistance ; Electric Impedance ; Female ; Flow cytometry ; Flow Cytometry - methods ; Hematology, Oncology and Palliative Medicine ; Humans ; Investigative techniques of hemodynamics ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Middle Aged ; Platelet Aggregation - drug effects ; Platelet Aggregation Inhibitors - pharmacology ; Platelets ; Thienopyridines ; Ticlopidine - analogs & derivatives ; Ticlopidine - pharmacology</subject><ispartof>Thrombosis research, 2007, Vol.121 (2), p.249-258</ispartof><rights>Elsevier Ltd</rights><rights>2007 Elsevier Ltd</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-399b3f1603fd146b1afb0ab9b7f2b4aa2fa905aa528a5df9c9e6a6e74dc8afe13</citedby><cites>FETCH-LOGICAL-c451t-399b3f1603fd146b1afb0ab9b7f2b4aa2fa905aa528a5df9c9e6a6e74dc8afe13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19885695$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17482663$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mueller, Thomas</creatorcontrib><creatorcontrib>Dieplinger, Benjamin</creatorcontrib><creatorcontrib>Poelz, Werner</creatorcontrib><creatorcontrib>Calatzis, Andreas</creatorcontrib><creatorcontrib>Haltmayer, Meinhard</creatorcontrib><title>Utility of whole blood impedance aggregometry for the assessment of clopidogrel action using the novel Multiplate® analyzer—comparison with two flow cytometric methods</title><title>Thrombosis research</title><addtitle>Thromb Res</addtitle><description>Abstract Background Non-responsiveness to anti-platelet therapy has been reported and has been linked to the occurrence of adverse events. No standard method to monitor clopidogrel efficacy is available at present. We aimed at comparing the utility of whole blood impedance aggregometry for the assessment of clopidogrel action using the novel Multiplate® analyzer with two flow cytometric methods. Methods Platelet function was determined before and after the initiation of clopidogrel therapy (300 mg loading dose, followed by 75 mg qd) in 40 patients (observational study). Furthermore, 77 patients and 77 referents with and without clopidogrel treatment (75 mg qd) were evaluated (case control study). Platelet function was assessed by Multiplate® ADP and ADP + PG tests, by P-selectin (CD62P) expression, and by vasodilator stimulated phosphoprotein (VASP) phosphorylation status. Results The observational study revealed that platelet reactivity decreased significantly after clopidogrel administration with all 4 methods ( p < 0.001 for each). In the case control study the median values of all 4 tests were significantly higher in the referents without clopidogrel treatment than in the patients on clopidogrel therapy ( p < 0.001 for each). Applying test specific lower reference limits as criterion for the differentiation between responders and non-responders to clopidogrel treatment, 57% of the patients on clopidogrel therapy were classified as non-responders with the Multiplate® ADP test, 38% with the Multiplate® ADP + PG test, 55% with the P-selectin assay, 9% with the PLT VASP/P2Y12 assay. Conclusions The VASP phosphorylation assay appeared to be advantageous for the assessment of clopidogrel action compared to the Multiplate® ADP + PG test, the P-selectin assay, and the Multiplate® ADP test (listed in descending order). However, our method comparison study underscores the critical nature of the dependence of results on the techniques used in specific studies, and it remains to be elucidated which method correlates best with the occurrence of adverse events.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aggregometry</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Brain</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular disease</subject><subject>Case-Control Studies</subject><subject>Clopidogrel</subject><subject>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</subject><subject>Drug Resistance</subject><subject>Electric Impedance</subject><subject>Female</subject><subject>Flow cytometry</subject><subject>Flow Cytometry - methods</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Investigative techniques of hemodynamics</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Platelet Aggregation - drug effects</subject><subject>Platelet Aggregation Inhibitors - pharmacology</subject><subject>Platelets</subject><subject>Thienopyridines</subject><subject>Ticlopidine - analogs & derivatives</subject><subject>Ticlopidine - pharmacology</subject><issn>0049-3848</issn><issn>1879-2472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFkktuFDEQhlsIRIbAFSJvYDeD3Q93e4NAUXhIQSwga8vtLs94cLcblzujZpVD5BQsOARH4SR4MoMisWFVUun7qyx_lWVnjK4YZfzldhU3wfcBcJVTWq9osaJ5_iBbsKYWy7ys84fZgtJSLIumbE6yJ4hbSlnNRPU4O2F12eScF4vsx1W0zsaZeEN2G--AtM77jth-hE4NGoharwOsfQ8xzMT4QOImNREBsYch7oPa-dF2PnGOKB2tH8iEdljfoYO_Tu2Pk4t2dCrCr59EDcrN3yH8vrnVvh9VsJgiOxs3JO48Mc7viJ7j3U6rSSob3-HT7JFRDuHZsZ5mV28vvpy_X15-evfh_M3lUpcVi8tCiLYwjNPCdKzkLVOmpaoVbW3ytlQqN0rQSqkqb1TVGaEFcMWhLjvdKAOsOM1eHOaOwX-bAKPsLWpwTg3gJ5S8qUpa8DKB_ADq4BEDGDkG26swS0bl3pLcyr-W5N6SpIVMllLw7Lhhanvo7mNHLQl4fgQUauVMSCYs3nOiaSouqsS9PnCQ_uPaQpCoLSRrnQ2go-y8_f9bXv0zQjs72LT1K8yAWz-FZAslk5hLKj_vb2p_UrRO55TurPgDtlXRjg</recordid><startdate>2007</startdate><enddate>2007</enddate><creator>Mueller, Thomas</creator><creator>Dieplinger, Benjamin</creator><creator>Poelz, Werner</creator><creator>Calatzis, Andreas</creator><creator>Haltmayer, Meinhard</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</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></search><sort><creationdate>2007</creationdate><title>Utility of whole blood impedance aggregometry for the assessment of clopidogrel action using the novel Multiplate® analyzer—comparison with two flow cytometric methods</title><author>Mueller, Thomas ; Dieplinger, Benjamin ; Poelz, Werner ; Calatzis, Andreas ; Haltmayer, Meinhard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-399b3f1603fd146b1afb0ab9b7f2b4aa2fa905aa528a5df9c9e6a6e74dc8afe13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aggregometry</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Brain</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular disease</topic><topic>Case-Control Studies</topic><topic>Clopidogrel</topic><topic>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</topic><topic>Drug Resistance</topic><topic>Electric Impedance</topic><topic>Female</topic><topic>Flow cytometry</topic><topic>Flow Cytometry - methods</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Investigative techniques of hemodynamics</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Platelet Aggregation - drug effects</topic><topic>Platelet Aggregation Inhibitors - pharmacology</topic><topic>Platelets</topic><topic>Thienopyridines</topic><topic>Ticlopidine - analogs & derivatives</topic><topic>Ticlopidine - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mueller, Thomas</creatorcontrib><creatorcontrib>Dieplinger, Benjamin</creatorcontrib><creatorcontrib>Poelz, Werner</creatorcontrib><creatorcontrib>Calatzis, Andreas</creatorcontrib><creatorcontrib>Haltmayer, Meinhard</creatorcontrib><collection>Pascal-Francis</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><jtitle>Thrombosis research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mueller, Thomas</au><au>Dieplinger, Benjamin</au><au>Poelz, Werner</au><au>Calatzis, Andreas</au><au>Haltmayer, Meinhard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Utility of whole blood impedance aggregometry for the assessment of clopidogrel action using the novel Multiplate® analyzer—comparison with two flow cytometric methods</atitle><jtitle>Thrombosis research</jtitle><addtitle>Thromb Res</addtitle><date>2007</date><risdate>2007</risdate><volume>121</volume><issue>2</issue><spage>249</spage><epage>258</epage><pages>249-258</pages><issn>0049-3848</issn><eissn>1879-2472</eissn><coden>THBRAA</coden><abstract>Abstract Background Non-responsiveness to anti-platelet therapy has been reported and has been linked to the occurrence of adverse events. No standard method to monitor clopidogrel efficacy is available at present. We aimed at comparing the utility of whole blood impedance aggregometry for the assessment of clopidogrel action using the novel Multiplate® analyzer with two flow cytometric methods. Methods Platelet function was determined before and after the initiation of clopidogrel therapy (300 mg loading dose, followed by 75 mg qd) in 40 patients (observational study). Furthermore, 77 patients and 77 referents with and without clopidogrel treatment (75 mg qd) were evaluated (case control study). Platelet function was assessed by Multiplate® ADP and ADP + PG tests, by P-selectin (CD62P) expression, and by vasodilator stimulated phosphoprotein (VASP) phosphorylation status. Results The observational study revealed that platelet reactivity decreased significantly after clopidogrel administration with all 4 methods ( p < 0.001 for each). In the case control study the median values of all 4 tests were significantly higher in the referents without clopidogrel treatment than in the patients on clopidogrel therapy ( p < 0.001 for each). Applying test specific lower reference limits as criterion for the differentiation between responders and non-responders to clopidogrel treatment, 57% of the patients on clopidogrel therapy were classified as non-responders with the Multiplate® ADP test, 38% with the Multiplate® ADP + PG test, 55% with the P-selectin assay, 9% with the PLT VASP/P2Y12 assay. Conclusions The VASP phosphorylation assay appeared to be advantageous for the assessment of clopidogrel action compared to the Multiplate® ADP + PG test, the P-selectin assay, and the Multiplate® ADP test (listed in descending order). However, our method comparison study underscores the critical nature of the dependence of results on the techniques used in specific studies, and it remains to be elucidated which method correlates best with the occurrence of adverse events.</abstract><cop>New York, NY</cop><pub>Elsevier Ltd</pub><pmid>17482663</pmid><doi>10.1016/j.thromres.2007.03.022</doi><tpages>10</tpages></addata></record> |
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subjects | Aged Aged, 80 and over Aggregometry Biological and medical sciences Blood and lymphatic vessels Brain Cardiology. Vascular system Cardiovascular disease Case-Control Studies Clopidogrel Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous Drug Resistance Electric Impedance Female Flow cytometry Flow Cytometry - methods Hematology, Oncology and Palliative Medicine Humans Investigative techniques of hemodynamics Investigative techniques, diagnostic techniques (general aspects) Male Medical sciences Middle Aged Platelet Aggregation - drug effects Platelet Aggregation Inhibitors - pharmacology Platelets Thienopyridines Ticlopidine - analogs & derivatives Ticlopidine - pharmacology |
title | Utility of whole blood impedance aggregometry for the assessment of clopidogrel action using the novel Multiplate® analyzer—comparison with two flow cytometric methods |
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