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dc.contributor.author Singh P
dc.contributor.author Emami H
dc.contributor.author Subramanian S
dc.contributor.author Maurovich-Horvat, Pál
dc.contributor.author Marincheva-Savcheva G
dc.contributor.author Medina HM
dc.contributor.author Abdelbaky A
dc.contributor.author Alon A
dc.contributor.author Shankar SS
dc.contributor.author Rudd JH
dc.contributor.author Fayad ZA
dc.contributor.author Hoffmann U
dc.contributor.author Tawakol A
dc.date.accessioned 2018-09-04T12:27:53Z
dc.date.available 2018-09-04T12:27:53Z
dc.date.issued 2016
dc.identifier 85007086496
dc.identifier.citation pagination=e004195, pages 9; journalVolume=9; journalIssueNumber=12; journalTitle=CIRCULATION-CARDIOVASCULAR IMAGING;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/5802
dc.identifier.uri doi:10.1161/CIRCIMAGING.115.004195
dc.description.abstract BACKGROUND: Nonobstructive coronary plaques manifesting high-risk morphology (HRM) associate with an increased risk of adverse clinical cardiovascular events. We sought to test the hypothesis that statins have a greater anti-inflammatory effect within coronary plaques containing HRM. METHODS AND RESULTS: In this prospective multicenter study, 55 subjects with or at high risk for atherosclerosis underwent 18F-fluorodeoxyglucose positron emission tomographic/computed tomographic imaging at baseline and after 12 weeks of treatment with atorvastatin. Coronary arterial inflammation (18F-fluorodeoxyglucose uptake, expressed as target-to-background ratio) was assessed in the left main coronary artery (LMCA). While blinded to the PET findings, contrast-enhanced computed tomographic angiography was performed to characterize the presence of HRM (defined as noncalcified or partially calcified plaques) in the LMCA. Arterial inflammation (target-to-background ratio) was higher in LMCA segments with HRM than those without HRM (mean+/-SEM: 1.95+/-0.43 versus 1.67+/-0.32 for LMCA with versus without HRM, respectively; P=0.04). Moreover, atorvastatin treatment for 12 weeks reduced target-to-background ratio more in LMCA segments with HRM than those without HRM (12 week-baseline Deltatarget-to-background ratio [95% confidence interval]: -0.18 [-0.35 to -0.004] versus 0.09 [-0.06 to 0.26]; P=0.02). Furthermore, this relationship between coronary plaque morphology and change in LMCA inflammatory activity remained significant after adjusting for baseline low-density lipoprotein and statin dose (beta=-0.27; P=0.038). CONCLUSIONS: In this first study to evaluate the impact of statins on coronary inflammation, we observed that the anti-inflammatory impact of statins is substantially greater within coronary plaques that contain HRM features. These findings suggest an additional mechanism by which statins disproportionately benefit individuals with more advanced atherosclerotic disease. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier: NCT00703261.
dc.relation.ispartof urn:issn:1941-9651
dc.title Coronary Plaque Morphology and the Anti-Inflammatory Impact of Atorvastatin: A Multicenter 18F-Fluorodeoxyglucose Positron Emission Tomographic/Computed Tomographic Study.
dc.type Journal Article
dc.date.updated 2018-07-13T11:03:23Z
dc.language.rfc3066 en
dc.identifier.mtmt 3153957
dc.identifier.wos 000391822800002
dc.identifier.pubmed 27956407
dc.contributor.department SE/AOK/K/VAROSMAJOR_SZÍVÉRGYÓGY/KARDI KZP_KARDIO-T/MTA-SE Lendület Kardiovaszkuláris Képalkotó Kutatócsoport [2017.10.31]
dc.contributor.institution Semmelweis Egyetem


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