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Use of Apolipoprotein B in the Era of Precision Medicine: Time for a Paradigm Change?

Atherosclerotic cardiovascular disease (ASCVD) remains the leading cause of death worldwide and the risk of a major cardiovascular event is highest among those with established disease. Ongoing management of these patients relies on the accurate assessment of their response to any prescribed therapy...

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Autores principales: Cole, Justine, Zubirán, Rafael, Wolska, Anna, Jialal, Ishwarlal, Remaley, Alan T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10488498/
https://www.ncbi.nlm.nih.gov/pubmed/37685804
http://dx.doi.org/10.3390/jcm12175737
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author Cole, Justine
Zubirán, Rafael
Wolska, Anna
Jialal, Ishwarlal
Remaley, Alan T.
author_facet Cole, Justine
Zubirán, Rafael
Wolska, Anna
Jialal, Ishwarlal
Remaley, Alan T.
author_sort Cole, Justine
collection PubMed
description Atherosclerotic cardiovascular disease (ASCVD) remains the leading cause of death worldwide and the risk of a major cardiovascular event is highest among those with established disease. Ongoing management of these patients relies on the accurate assessment of their response to any prescribed therapy, and their residual risk, in order to optimize treatment. Recent international guidelines and position statements concur that the plasma concentration of apolipoprotein B (apoB) is the most accurate measure of lipoprotein associated ASCVD risk. This is especially true for the growing number of individuals with diabetes, obesity, or the metabolic syndrome, and those on statin therapy. Most guidelines, however, continue to promote LDL-C as the primary risk marker due to uncertainty as to whether the greater accuracy of apoB is sufficient to warrant a paradigm shift. Recommendations regarding apoB measurement vary, and the information provided on how to interpret apoB results is sometimes insufficient, particularly for non-lipid specialists. Misinformation regarding the reliability of the assays is also frequently repeated despite its equivalent or better standardization than many other diagnostic assays. Thus, demand for apoB testing is relatively low, which means there is little incentive to increase its availability or reduce its cost. In this review, we examine the results of recent clinical outcomes studies and meta-analyses on the relative values of apoB, LDL-C, and non-HDL-C as markers of ASCVD risk. Although there is seemingly minimal difference among these markers when only population-based metrics are considered, it is evident from our analysis that, from a personalized or precision medicine standpoint, many individuals would benefit, at a negligible total cost, if apoB measurement were better integrated into the diagnosis and treatment of ASCVD.
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spelling pubmed-104884982023-09-09 Use of Apolipoprotein B in the Era of Precision Medicine: Time for a Paradigm Change? Cole, Justine Zubirán, Rafael Wolska, Anna Jialal, Ishwarlal Remaley, Alan T. J Clin Med Review Atherosclerotic cardiovascular disease (ASCVD) remains the leading cause of death worldwide and the risk of a major cardiovascular event is highest among those with established disease. Ongoing management of these patients relies on the accurate assessment of their response to any prescribed therapy, and their residual risk, in order to optimize treatment. Recent international guidelines and position statements concur that the plasma concentration of apolipoprotein B (apoB) is the most accurate measure of lipoprotein associated ASCVD risk. This is especially true for the growing number of individuals with diabetes, obesity, or the metabolic syndrome, and those on statin therapy. Most guidelines, however, continue to promote LDL-C as the primary risk marker due to uncertainty as to whether the greater accuracy of apoB is sufficient to warrant a paradigm shift. Recommendations regarding apoB measurement vary, and the information provided on how to interpret apoB results is sometimes insufficient, particularly for non-lipid specialists. Misinformation regarding the reliability of the assays is also frequently repeated despite its equivalent or better standardization than many other diagnostic assays. Thus, demand for apoB testing is relatively low, which means there is little incentive to increase its availability or reduce its cost. In this review, we examine the results of recent clinical outcomes studies and meta-analyses on the relative values of apoB, LDL-C, and non-HDL-C as markers of ASCVD risk. Although there is seemingly minimal difference among these markers when only population-based metrics are considered, it is evident from our analysis that, from a personalized or precision medicine standpoint, many individuals would benefit, at a negligible total cost, if apoB measurement were better integrated into the diagnosis and treatment of ASCVD. MDPI 2023-09-03 /pmc/articles/PMC10488498/ /pubmed/37685804 http://dx.doi.org/10.3390/jcm12175737 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 Review
Cole, Justine
Zubirán, Rafael
Wolska, Anna
Jialal, Ishwarlal
Remaley, Alan T.
Use of Apolipoprotein B in the Era of Precision Medicine: Time for a Paradigm Change?
title Use of Apolipoprotein B in the Era of Precision Medicine: Time for a Paradigm Change?
title_full Use of Apolipoprotein B in the Era of Precision Medicine: Time for a Paradigm Change?
title_fullStr Use of Apolipoprotein B in the Era of Precision Medicine: Time for a Paradigm Change?
title_full_unstemmed Use of Apolipoprotein B in the Era of Precision Medicine: Time for a Paradigm Change?
title_short Use of Apolipoprotein B in the Era of Precision Medicine: Time for a Paradigm Change?
title_sort use of apolipoprotein b in the era of precision medicine: time for a paradigm change?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10488498/
https://www.ncbi.nlm.nih.gov/pubmed/37685804
http://dx.doi.org/10.3390/jcm12175737
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