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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8540246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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