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dc.contributor.authorBrügger-Andersen, Trygveeng
dc.contributor.authorBostad, Leifeng
dc.contributor.authorSandnes, Dagny A.eng
dc.contributor.authorLarsen, Alf Ingeeng
dc.contributor.authorBonarjee, Vernon V. S.eng
dc.contributor.authorBarvik, Ståleeng
dc.contributor.authorMelberg, Toreng
dc.contributor.authorNilsen, Dennis W. T.eng
dc.date.accessioned2011-04-29T06:48:56Z
dc.date.available2011-04-29T06:48:56Z
dc.date.issued2010-01-27eng
dc.identifier.citationThrombosis Journal 8:1en_US
dc.identifier.issn1477-9560eng
dc.identifier.urihttp://hdl.handle.net/1956/4714
dc.description.abstractBackground The expression of pregnancy-associated plasma protein A (PAPP-A) was identified by immunohistochemistry (IHC) in culprit atherothrombotic plaque specimens harvested from patients admitted with ST-segment elevation myocardial infarction (STEMI). Methods The atherothrombotic samples were collected from a consecutive cohort consisting of 20 individuals admitted with STEMI to Stavanger University Hospital, Norway, from 2005-2006, presenting angiographically with an acute thrombotic occlusion of a coronary artery characterized by TIMI flow 0. The atherothrombotic plaques were obtained by aspiration thrombectomy during percutaneous coronary intervention within 12 hours from the onset of symptoms and prepared for IHC analysis. Results In the IHC analysis staining for PAPP-A occurred in the extracellular matrix of the plaques and no evidence of staining for PAPP-A was found in the thrombi. Conclusion Our results indicate that in vivo PAPP-A is strongly expressed in atherothrombotic plaques harvested from patients admitted with STEMI, as documented by IHC.en_US
dc.language.isoengeng
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/2.0eng
dc.titleThe activity of pregnancy-associated plasma protein A (PAPP-A) as expressed by immunohistochemistry in atherothrombotic plaques obtained by aspiration thrombectomy in patients presenting with a ST-elevation myocardial infarction: a brief communicationeng
dc.typeJournal articleeng
dc.typePeer reviewedeng
dc.rights.holderCopyright 2010 Brügger-Andersen et al; licensee BioMed Central Ltd.
dc.rights.holderBrügger-Andersen et al.eng
dc.type.versionpublishedVersioneng
bora.peerreviewedPeer reviewedeng
bora.cristinID348392eng
bibo.doihttp://dx.doi.org/10.1186/1477-9560-8-1eng
dc.identifier.cristinID348392eng
dc.identifier.doihttp://dx.doi.org/10.1186/1477-9560-8-1


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