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Apolipoprotein B and Cardiovascular Disease: Biomarker and Potential Therapeutic Target

Apolipoprotein (apo) B, the critical structural protein of the atherogenic lipoproteins, has two major isoforms: apoB48 and apoB100. ApoB48 is found in chylomicrons and chylomicron remnants with one apoB48 molecule per chylomicron particle. Similarly, a single apoB100 molecule is contained per parti...

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Autores principales: Behbodikhah, Jennifer, Ahmed, Saba, Elyasi, Ailin, Kasselman, Lora J., De Leon, Joshua, Glass, Amy D., Reiss, Allison B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8540246/
https://www.ncbi.nlm.nih.gov/pubmed/34677405
http://dx.doi.org/10.3390/metabo11100690
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author Behbodikhah, Jennifer
Ahmed, Saba
Elyasi, Ailin
Kasselman, Lora J.
De Leon, Joshua
Glass, Amy D.
Reiss, Allison B.
author_facet Behbodikhah, Jennifer
Ahmed, Saba
Elyasi, Ailin
Kasselman, Lora J.
De Leon, Joshua
Glass, Amy D.
Reiss, Allison B.
author_sort Behbodikhah, Jennifer
collection PubMed
description Apolipoprotein (apo) B, the critical structural protein of the atherogenic lipoproteins, has two major isoforms: apoB48 and apoB100. ApoB48 is found in chylomicrons and chylomicron remnants with one apoB48 molecule per chylomicron particle. Similarly, a single apoB100 molecule is contained per particle of very-low-density lipoprotein (VLDL), intermediate density lipoprotein, LDL and lipoprotein(a). This unique one apoB per particle ratio makes plasma apoB concentration a direct measure of the number of circulating atherogenic lipoproteins. ApoB levels indicate the atherogenic particle concentration independent of the particle cholesterol content, which is variable. While LDL, the major cholesterol-carrying serum lipoprotein, is the primary therapeutic target for management and prevention of atherosclerotic cardiovascular disease, there is strong evidence that apoB is a more accurate indicator of cardiovascular risk than either total cholesterol or LDL cholesterol. This review examines multiple aspects of apoB structure and function, with a focus on the controversy over use of apoB as a therapeutic target in clinical practice. Ongoing coronary artery disease residual risk, despite lipid-lowering treatment, has left patients and clinicians with unsatisfactory options for monitoring cardiovascular health. At the present time, the substitution of apoB for LDL-C in cardiovascular disease prevention guidelines has been deemed unjustified, but discussions continue.
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spelling pubmed-85402462021-10-24 Apolipoprotein B and Cardiovascular Disease: Biomarker and Potential Therapeutic Target Behbodikhah, Jennifer Ahmed, Saba Elyasi, Ailin Kasselman, Lora J. De Leon, Joshua Glass, Amy D. Reiss, Allison B. Metabolites Review Apolipoprotein (apo) B, the critical structural protein of the atherogenic lipoproteins, has two major isoforms: apoB48 and apoB100. ApoB48 is found in chylomicrons and chylomicron remnants with one apoB48 molecule per chylomicron particle. Similarly, a single apoB100 molecule is contained per particle of very-low-density lipoprotein (VLDL), intermediate density lipoprotein, LDL and lipoprotein(a). This unique one apoB per particle ratio makes plasma apoB concentration a direct measure of the number of circulating atherogenic lipoproteins. ApoB levels indicate the atherogenic particle concentration independent of the particle cholesterol content, which is variable. While LDL, the major cholesterol-carrying serum lipoprotein, is the primary therapeutic target for management and prevention of atherosclerotic cardiovascular disease, there is strong evidence that apoB is a more accurate indicator of cardiovascular risk than either total cholesterol or LDL cholesterol. This review examines multiple aspects of apoB structure and function, with a focus on the controversy over use of apoB as a therapeutic target in clinical practice. Ongoing coronary artery disease residual risk, despite lipid-lowering treatment, has left patients and clinicians with unsatisfactory options for monitoring cardiovascular health. At the present time, the substitution of apoB for LDL-C in cardiovascular disease prevention guidelines has been deemed unjustified, but discussions continue. MDPI 2021-10-08 /pmc/articles/PMC8540246/ /pubmed/34677405 http://dx.doi.org/10.3390/metabo11100690 Text en © 2021 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
Behbodikhah, Jennifer
Ahmed, Saba
Elyasi, Ailin
Kasselman, Lora J.
De Leon, Joshua
Glass, Amy D.
Reiss, Allison B.
Apolipoprotein B and Cardiovascular Disease: Biomarker and Potential Therapeutic Target
title Apolipoprotein B and Cardiovascular Disease: Biomarker and Potential Therapeutic Target
title_full Apolipoprotein B and Cardiovascular Disease: Biomarker and Potential Therapeutic Target
title_fullStr Apolipoprotein B and Cardiovascular Disease: Biomarker and Potential Therapeutic Target
title_full_unstemmed Apolipoprotein B and Cardiovascular Disease: Biomarker and Potential Therapeutic Target
title_short Apolipoprotein B and Cardiovascular Disease: Biomarker and Potential Therapeutic Target
title_sort apolipoprotein b and cardiovascular disease: biomarker and potential therapeutic target
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8540246/
https://www.ncbi.nlm.nih.gov/pubmed/34677405
http://dx.doi.org/10.3390/metabo11100690
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