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Dynamic nature of nonculprit coronary artery lesion morphology in STEMI: a serial IVUS analysis from the HORIZONS-AMI trial.

DC Field Value Language
dc.contributor.authorZhao, Z-
dc.contributor.authorWitzenbichler, B-
dc.contributor.authorMintz, GS-
dc.contributor.authorJaster, M-
dc.contributor.authorChoi, SY-
dc.contributor.authorWu, X-
dc.contributor.authorHe, Y-
dc.contributor.authorMargolis, MP-
dc.contributor.authorDressler, O-
dc.contributor.authorCristea, E-
dc.contributor.authorParise, H-
dc.contributor.authorMehran, R-
dc.contributor.authorStone, GW-
dc.contributor.authorMaehara, A-
dc.date.accessioned2014-05-19T04:28:33Z-
dc.date.available2014-05-19T04:28:33Z-
dc.date.issued2013-
dc.identifier.issn1936-878X-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/9991-
dc.description.abstractOBJECTIVES: The authors sought to report the temporal stability of an untreated, nonculprit lesion phenotype in patients presenting with ST-segment elevation myocardial infarction (STEMI).



BACKGROUND: The temporal stability of the untreated, nonculprit lesion phenotype has been studied using intravascular ultrasound-virtual histology (IVUS) in patients with stable ischemic heart disease, but not in STEMI patients.



METHODS: As part of a formal substudy of the HORIZONS-AMI (Harmonizing Outcomes With Revascularization and Stents in Acute Myocardial Infarction) trial, baseline and 13-month follow-up IVUS was performed in 99 untreated nonculprit lesions in 63 STEMI patients. Lesions were classified as pathological intimal thickening (PIT), IVUS-derived thin-cap fibroatheroma (TCFA), thick-cap fibroatheroma (ThCFA), fibrotic plaque, or fibrocalcific plaque.



RESULTS: The frequency of TCFA increased from 41% at baseline to 54% at follow-up, whereas ThCFAs decreased from 41% to 34% and PIT decreased from 16% to 8%. Among the 41 lesions classified at baseline as TCFA, at follow-up, 32 (78%) were still classified as TCFA, whereas 9 (22%) were classified as ThCFAs or fibrotic plaques. An additional 21 lesions at follow-up were newly classified as TCFA, developing from either PIT or ThCFA. TCFA at baseline that evolved into non-TCFAs trended toward a more distal location than TCFA that did not change (p = 0.12). In lesions classified as TCFA, the minimum lumen area (MLA) decreased from 8.1 (interquartile range [IQR]: 7.4 to 8.8) mm(2) at baseline to 7.8 (IQR: 7.2 to 8.4) mm(2) at follow-up, p < 0.05; this was associated with an increase in percent necrotic core at the MLA site (14% [IQR: 12 to 16] to 19% [IQR: 17 to 22], p < 0.0001) and over the entire length of the lesion (14% [IQR: 12 to 16] to 18% [IQR: 17 to 20], p < 0.0001).



CONCLUSIONS: Untreated nonculprit lesions in STEMI patients frequently have TCFA morphology that does not change during 13-month follow-up and is accompanied by a decrease in MLA and an increase in necrotic core. (Harmonizing Outcomes With Revascularization and Stents in Acute Myocardial Infarction [HORIZONS-AMI]; NCT00433966).
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dc.language.isoen-
dc.subject.MESHAged-
dc.subject.MESHAnticoagulants-
dc.subject.MESHChi-Square Distribution-
dc.subject.MESHCoronary Artery Disease-
dc.subject.MESHCoronary Vessels-
dc.subject.MESHFemale-
dc.subject.MESHFibrosis-
dc.subject.MESHHumans-
dc.subject.MESHLeast-Squares Analysis-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMyocardial Infarction-
dc.subject.MESHMyocardial Revascularization-
dc.subject.MESHNecrosis-
dc.subject.MESHPlaque, Atherosclerotic-
dc.subject.MESHPlatelet Aggregation Inhibitors-
dc.subject.MESHPredictive Value of Tests-
dc.subject.MESHStents-
dc.subject.MESHTime Factors-
dc.subject.MESHTreatment Outcome-
dc.subject.MESHUltrasonography, Interventional-
dc.titleDynamic nature of nonculprit coronary artery lesion morphology in STEMI: a serial IVUS analysis from the HORIZONS-AMI trial.-
dc.typeArticle-
dc.identifier.pmid23328566-
dc.identifier.urlhttp://linkinghub.elsevier.com/retrieve/pii/S1936-878X(12)00875-3-
dc.contributor.affiliatedAuthor최, 소연-
dc.type.localJournal Papers-
dc.identifier.doi10.1016/j.jcmg.2012.08.010-
dc.citation.titleJACC. Cardiovascular imaging-
dc.citation.volume6-
dc.citation.number1-
dc.citation.date2013-
dc.citation.startPage86-
dc.citation.endPage95-
dc.identifier.bibliographicCitationJACC. Cardiovascular imaging, 6(1). : 86-95, 2013-
dc.identifier.eissn1876-7591-
dc.relation.journalidJ01936878X-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Cardiology
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