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Serum Soluble Lectin-like Oxidized Low-Density Lipoprotein Receptor-1 (sLOX-1) Is Associated with Atherosclerosis Severity in Coronary Artery Disease

Risk-factor-based scoring systems for atherosclerotic coronary artery disease (CAD) remain concerningly inaccurate at the level of the individual and would benefit from the addition of biomarkers that correlate with atherosclerosis burden directly. We hypothesized that serum soluble lectin-like oxid...

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Autores principales: Kott, Katharine A., Genetzakis, Elijah, Gray, Michael P., Hansen, Peter, McGuire, Helen M., Yang, Jean Y., Grieve, Stuart M., Vernon, Stephen T., Figtree, Gemma A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452248/
https://www.ncbi.nlm.nih.gov/pubmed/37627252
http://dx.doi.org/10.3390/biom13081187
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author Kott, Katharine A.
Genetzakis, Elijah
Gray, Michael P.
Hansen, Peter
McGuire, Helen M.
Yang, Jean Y.
Grieve, Stuart M.
Vernon, Stephen T.
Figtree, Gemma A.
author_facet Kott, Katharine A.
Genetzakis, Elijah
Gray, Michael P.
Hansen, Peter
McGuire, Helen M.
Yang, Jean Y.
Grieve, Stuart M.
Vernon, Stephen T.
Figtree, Gemma A.
author_sort Kott, Katharine A.
collection PubMed
description Risk-factor-based scoring systems for atherosclerotic coronary artery disease (CAD) remain concerningly inaccurate at the level of the individual and would benefit from the addition of biomarkers that correlate with atherosclerosis burden directly. We hypothesized that serum soluble lectin-like oxidized low-density lipoprotein receptor-1 (sLOX-1) would be independently associated with CAD and investigated this in the BioHEART study using 968 participants with CT coronary angiograms, which were scored for disease burden in the form of coronary artery calcium scores (CACS), Gensini scores, and a semi-quantitative soft-plaque score (SPS). Serum sLOX-1 was assessed by ELISA and was incorporated into regression models for disease severity and incidence. We demonstrate that sLOX-1 is associated with an improvement in the prediction of CAD severity when scored by Gensini or SPS, but not CACS. sLOX-1 also significantly improved the prediction of the incidence of obstructive CAD, defined as stenosis in any vessel >75%. The predictive value of sLOX-1 was significantly greater in the subgroup of patients who did not have any of the standard modifiable cardiovascular risk factors (SMuRFs). sLOX-1 is associated with CAD severity and is the first biomarker shown to have utility for risk prediction in the SMuRFless population.
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spelling pubmed-104522482023-08-26 Serum Soluble Lectin-like Oxidized Low-Density Lipoprotein Receptor-1 (sLOX-1) Is Associated with Atherosclerosis Severity in Coronary Artery Disease Kott, Katharine A. Genetzakis, Elijah Gray, Michael P. Hansen, Peter McGuire, Helen M. Yang, Jean Y. Grieve, Stuart M. Vernon, Stephen T. Figtree, Gemma A. Biomolecules Article Risk-factor-based scoring systems for atherosclerotic coronary artery disease (CAD) remain concerningly inaccurate at the level of the individual and would benefit from the addition of biomarkers that correlate with atherosclerosis burden directly. We hypothesized that serum soluble lectin-like oxidized low-density lipoprotein receptor-1 (sLOX-1) would be independently associated with CAD and investigated this in the BioHEART study using 968 participants with CT coronary angiograms, which were scored for disease burden in the form of coronary artery calcium scores (CACS), Gensini scores, and a semi-quantitative soft-plaque score (SPS). Serum sLOX-1 was assessed by ELISA and was incorporated into regression models for disease severity and incidence. We demonstrate that sLOX-1 is associated with an improvement in the prediction of CAD severity when scored by Gensini or SPS, but not CACS. sLOX-1 also significantly improved the prediction of the incidence of obstructive CAD, defined as stenosis in any vessel >75%. The predictive value of sLOX-1 was significantly greater in the subgroup of patients who did not have any of the standard modifiable cardiovascular risk factors (SMuRFs). sLOX-1 is associated with CAD severity and is the first biomarker shown to have utility for risk prediction in the SMuRFless population. MDPI 2023-07-29 /pmc/articles/PMC10452248/ /pubmed/37627252 http://dx.doi.org/10.3390/biom13081187 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kott, Katharine A.
Genetzakis, Elijah
Gray, Michael P.
Hansen, Peter
McGuire, Helen M.
Yang, Jean Y.
Grieve, Stuart M.
Vernon, Stephen T.
Figtree, Gemma A.
Serum Soluble Lectin-like Oxidized Low-Density Lipoprotein Receptor-1 (sLOX-1) Is Associated with Atherosclerosis Severity in Coronary Artery Disease
title Serum Soluble Lectin-like Oxidized Low-Density Lipoprotein Receptor-1 (sLOX-1) Is Associated with Atherosclerosis Severity in Coronary Artery Disease
title_full Serum Soluble Lectin-like Oxidized Low-Density Lipoprotein Receptor-1 (sLOX-1) Is Associated with Atherosclerosis Severity in Coronary Artery Disease
title_fullStr Serum Soluble Lectin-like Oxidized Low-Density Lipoprotein Receptor-1 (sLOX-1) Is Associated with Atherosclerosis Severity in Coronary Artery Disease
title_full_unstemmed Serum Soluble Lectin-like Oxidized Low-Density Lipoprotein Receptor-1 (sLOX-1) Is Associated with Atherosclerosis Severity in Coronary Artery Disease
title_short Serum Soluble Lectin-like Oxidized Low-Density Lipoprotein Receptor-1 (sLOX-1) Is Associated with Atherosclerosis Severity in Coronary Artery Disease
title_sort serum soluble lectin-like oxidized low-density lipoprotein receptor-1 (slox-1) is associated with atherosclerosis severity in coronary artery disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452248/
https://www.ncbi.nlm.nih.gov/pubmed/37627252
http://dx.doi.org/10.3390/biom13081187
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