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Data on the lipoprotein (a), coronary atherosclerotic burden and vulnerable plaque phenotype in angiographic obstructive coronary artery disease

Lipoprotein Lp(a) represents an independent risk factor for coronary artery disease (CAD). However, its association with CAD burden and lipid rich plaques prone to rupture in patients with acute coronary syndrome (ACS) still remains unknown. These data aim to investigate the association among serum...

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Autores principales: Niccoli, Giampaolo, Chin, Diana, Scalone, Giancarla, Panebianco, Mario, Abbolito, Sofia, Cosentino, Nicola, Jacoangeli, Francesca, Refaat, Hesham, Gallo, Giovanna, Salerno, Gerardo, Volpe, Massimo, Crea, Filippo, De Biase, Luciano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4845071/
https://www.ncbi.nlm.nih.gov/pubmed/27158659
http://dx.doi.org/10.1016/j.dib.2016.04.017
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author Niccoli, Giampaolo
Chin, Diana
Scalone, Giancarla
Panebianco, Mario
Abbolito, Sofia
Cosentino, Nicola
Jacoangeli, Francesca
Refaat, Hesham
Gallo, Giovanna
Salerno, Gerardo
Volpe, Massimo
Crea, Filippo
De Biase, Luciano
author_facet Niccoli, Giampaolo
Chin, Diana
Scalone, Giancarla
Panebianco, Mario
Abbolito, Sofia
Cosentino, Nicola
Jacoangeli, Francesca
Refaat, Hesham
Gallo, Giovanna
Salerno, Gerardo
Volpe, Massimo
Crea, Filippo
De Biase, Luciano
author_sort Niccoli, Giampaolo
collection PubMed
description Lipoprotein Lp(a) represents an independent risk factor for coronary artery disease (CAD). However, its association with CAD burden and lipid rich plaques prone to rupture in patients with acute coronary syndrome (ACS) still remains unknown. These data aim to investigate the association among serum Lipoprotein(a) (Lpa) levels, coronary atherosclerotic burden and features of culprit plaque in patients with ACS and obstructive CAD. For his reason, a total of 500 ACS patients were enrolled for the angiographic cohort and 51 ACS patients were enrolled for the optical coherence tomography (OCT) cohort. Angiographic CAD severity was assessed by Sullivan score and by Bogaty score including stenosis score and extent index, whereas OCT plaque features were evaluated at the site of the minimal lumen area and along the culprit segment. In the angiographic cohort, Lp(a) was a weak independent predictor of Sullivan score (p<0.0001), stenosis score (p<0.0001) and extent index (p<0.0001). In the OCT cohort, patients with higher Lp(a) levels (>30 md/dl) compared to patients with lower Lp(a) levels (<30 md/dl) exhibited a higher prevalence of lipidic plaque at the site of the culprit stenosis (P=0.02), a wider lipid arc (p=0.003) and a higher prevalence of thin-cap fibroatheroma (p=0.004)
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spelling pubmed-48450712016-05-06 Data on the lipoprotein (a), coronary atherosclerotic burden and vulnerable plaque phenotype in angiographic obstructive coronary artery disease Niccoli, Giampaolo Chin, Diana Scalone, Giancarla Panebianco, Mario Abbolito, Sofia Cosentino, Nicola Jacoangeli, Francesca Refaat, Hesham Gallo, Giovanna Salerno, Gerardo Volpe, Massimo Crea, Filippo De Biase, Luciano Data Brief Data Article Lipoprotein Lp(a) represents an independent risk factor for coronary artery disease (CAD). However, its association with CAD burden and lipid rich plaques prone to rupture in patients with acute coronary syndrome (ACS) still remains unknown. These data aim to investigate the association among serum Lipoprotein(a) (Lpa) levels, coronary atherosclerotic burden and features of culprit plaque in patients with ACS and obstructive CAD. For his reason, a total of 500 ACS patients were enrolled for the angiographic cohort and 51 ACS patients were enrolled for the optical coherence tomography (OCT) cohort. Angiographic CAD severity was assessed by Sullivan score and by Bogaty score including stenosis score and extent index, whereas OCT plaque features were evaluated at the site of the minimal lumen area and along the culprit segment. In the angiographic cohort, Lp(a) was a weak independent predictor of Sullivan score (p<0.0001), stenosis score (p<0.0001) and extent index (p<0.0001). In the OCT cohort, patients with higher Lp(a) levels (>30 md/dl) compared to patients with lower Lp(a) levels (<30 md/dl) exhibited a higher prevalence of lipidic plaque at the site of the culprit stenosis (P=0.02), a wider lipid arc (p=0.003) and a higher prevalence of thin-cap fibroatheroma (p=0.004) Elsevier 2016-04-13 /pmc/articles/PMC4845071/ /pubmed/27158659 http://dx.doi.org/10.1016/j.dib.2016.04.017 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Data Article
Niccoli, Giampaolo
Chin, Diana
Scalone, Giancarla
Panebianco, Mario
Abbolito, Sofia
Cosentino, Nicola
Jacoangeli, Francesca
Refaat, Hesham
Gallo, Giovanna
Salerno, Gerardo
Volpe, Massimo
Crea, Filippo
De Biase, Luciano
Data on the lipoprotein (a), coronary atherosclerotic burden and vulnerable plaque phenotype in angiographic obstructive coronary artery disease
title Data on the lipoprotein (a), coronary atherosclerotic burden and vulnerable plaque phenotype in angiographic obstructive coronary artery disease
title_full Data on the lipoprotein (a), coronary atherosclerotic burden and vulnerable plaque phenotype in angiographic obstructive coronary artery disease
title_fullStr Data on the lipoprotein (a), coronary atherosclerotic burden and vulnerable plaque phenotype in angiographic obstructive coronary artery disease
title_full_unstemmed Data on the lipoprotein (a), coronary atherosclerotic burden and vulnerable plaque phenotype in angiographic obstructive coronary artery disease
title_short Data on the lipoprotein (a), coronary atherosclerotic burden and vulnerable plaque phenotype in angiographic obstructive coronary artery disease
title_sort data on the lipoprotein (a), coronary atherosclerotic burden and vulnerable plaque phenotype in angiographic obstructive coronary artery disease
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4845071/
https://www.ncbi.nlm.nih.gov/pubmed/27158659
http://dx.doi.org/10.1016/j.dib.2016.04.017
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