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Association between LDL-C, Non HDL-C, and Apolipoprotein B Levels with Coronary Plaque Regression

BACKGROUND: Previous reports have inferred a linear relationship between LDL-C and changes in coronary plaque volume (CPV) measured by intravascular ultrasound. However, these publications included a small number of studies and did not explore other lipid markers. OBJECTIVE: To assess the associatio...

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Autores principales: Masson, Walter, Siniawski, Daniel, Lobo, Martín, Molinero, Graciela, Giorgi, Mariano, Huerín, Melina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Cardiologia 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4523283/
https://www.ncbi.nlm.nih.gov/pubmed/26016784
http://dx.doi.org/10.5935/abc.20150050
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author Masson, Walter
Siniawski, Daniel
Lobo, Martín
Molinero, Graciela
Giorgi, Mariano
Huerín, Melina
author_facet Masson, Walter
Siniawski, Daniel
Lobo, Martín
Molinero, Graciela
Giorgi, Mariano
Huerín, Melina
author_sort Masson, Walter
collection PubMed
description BACKGROUND: Previous reports have inferred a linear relationship between LDL-C and changes in coronary plaque volume (CPV) measured by intravascular ultrasound. However, these publications included a small number of studies and did not explore other lipid markers. OBJECTIVE: To assess the association between changes in lipid markers and regression of CPV using published data. METHODS: We collected data from the control, placebo and intervention arms in studies that compared the effect of lipidlowering treatments on CPV, and from the placebo and control arms in studies that tested drugs that did not affect lipids. Baseline and final measurements of plaque volume, expressed in mm(3), were extracted and the percentage changes after the interventions were calculated. Performing three linear regression analyses, we assessed the relationship between percentage and absolute changes in lipid markers and percentage variations in CPV. RESULTS: Twenty-seven studies were selected. Correlations between percentage changes in LDL-C, non-HDL-C, and apolipoprotein B (ApoB) and percentage changes in CPV were moderate (r = 0.48, r = 0.47, and r = 0.44, respectively). Correlations between absolute differences in LDL-C, non‑HDL-C, and ApoB with percentage differences in CPV were stronger (r = 0.57, r = 0.52, and r = 0.79). The linear regression model showed a statistically significant association between a reduction in lipid markers and regression of plaque volume. CONCLUSION: A significant association between changes in different atherogenic particles and regression of CPV was observed. The absolute reduction in ApoB showed the strongest correlation with coronary plaque regression.
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spelling pubmed-45232832015-08-07 Association between LDL-C, Non HDL-C, and Apolipoprotein B Levels with Coronary Plaque Regression Masson, Walter Siniawski, Daniel Lobo, Martín Molinero, Graciela Giorgi, Mariano Huerín, Melina Arq Bras Cardiol Original Articles BACKGROUND: Previous reports have inferred a linear relationship between LDL-C and changes in coronary plaque volume (CPV) measured by intravascular ultrasound. However, these publications included a small number of studies and did not explore other lipid markers. OBJECTIVE: To assess the association between changes in lipid markers and regression of CPV using published data. METHODS: We collected data from the control, placebo and intervention arms in studies that compared the effect of lipidlowering treatments on CPV, and from the placebo and control arms in studies that tested drugs that did not affect lipids. Baseline and final measurements of plaque volume, expressed in mm(3), were extracted and the percentage changes after the interventions were calculated. Performing three linear regression analyses, we assessed the relationship between percentage and absolute changes in lipid markers and percentage variations in CPV. RESULTS: Twenty-seven studies were selected. Correlations between percentage changes in LDL-C, non-HDL-C, and apolipoprotein B (ApoB) and percentage changes in CPV were moderate (r = 0.48, r = 0.47, and r = 0.44, respectively). Correlations between absolute differences in LDL-C, non‑HDL-C, and ApoB with percentage differences in CPV were stronger (r = 0.57, r = 0.52, and r = 0.79). The linear regression model showed a statistically significant association between a reduction in lipid markers and regression of plaque volume. CONCLUSION: A significant association between changes in different atherogenic particles and regression of CPV was observed. The absolute reduction in ApoB showed the strongest correlation with coronary plaque regression. Sociedade Brasileira de Cardiologia 2015-07 /pmc/articles/PMC4523283/ /pubmed/26016784 http://dx.doi.org/10.5935/abc.20150050 Text en http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution NonCommercial License which permits unrestricted noncommercial use, distribution, and reproduction in any medium provided the original work is properly cited.
spellingShingle Original Articles
Masson, Walter
Siniawski, Daniel
Lobo, Martín
Molinero, Graciela
Giorgi, Mariano
Huerín, Melina
Association between LDL-C, Non HDL-C, and Apolipoprotein B Levels with Coronary Plaque Regression
title Association between LDL-C, Non HDL-C, and Apolipoprotein B Levels with Coronary Plaque Regression
title_full Association between LDL-C, Non HDL-C, and Apolipoprotein B Levels with Coronary Plaque Regression
title_fullStr Association between LDL-C, Non HDL-C, and Apolipoprotein B Levels with Coronary Plaque Regression
title_full_unstemmed Association between LDL-C, Non HDL-C, and Apolipoprotein B Levels with Coronary Plaque Regression
title_short Association between LDL-C, Non HDL-C, and Apolipoprotein B Levels with Coronary Plaque Regression
title_sort association between ldl-c, non hdl-c, and apolipoprotein b levels with coronary plaque regression
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4523283/
https://www.ncbi.nlm.nih.gov/pubmed/26016784
http://dx.doi.org/10.5935/abc.20150050
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