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Remnant cholesterol and particle number of VLDL subfractions in coronary artery disease: Pros and cons

Mia O Johansen*, Signe Vedel-Krogh, Sune Fallgaard Nielsen, Shoaib Afzal, George Davey Smith, Børge G. Nordestgaard*

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

Abstract

Emerging evidence from large observational studies and causal genetic studies suggest that elevated very-low-density lipoproteins (VLDL) are important and independent risk factors for atherosclerosis, myocardial infarction, and coronary artery disease. The cholesterol content of VLDL particles is often combined as overall remnant cholesterol; however, VLDL particles encompasses a heterogeneous group of lipoproteins that vary significantly in size, density, and structural composition, contributing to metabolic heterogeneity of VLDL particles. This heterogeneity has been suggested important for understanding the atherogenicity of VLDL particles. Nevertheless, remnant cholesterol lack precision to capture metabolic heterogeneity of VLDL subfractions; in contrast, advanced techniques such as nuclear magnetic resonance (NMR) spectroscopy provide more accurate estimates of VLDL particle number and cholesterol content across subfractions.

This review aims at summarizing current evidence of the association between remnant cholesterol and particle number of VLDL subfractions as risk factors for myocardial infarction and coronary artery disease including pros and cons for using easily accessible remnant cholesterol versus using more advanced measurement methods for estimation of particle number of VLDL subfractions.
Original languageEnglish
Article number120605
JournalAtherosclerosis
Volume412
Early online date25 Nov 2025
DOIs
Publication statusE-pub ahead of print - 25 Nov 2025

Bibliographical note

Publisher Copyright:
© 2025 The Authors.

Research Groups and Themes

  • Bristol Population Health Science Institute

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  • Integrative Epidemiology Unit

    Davey Smith, G. (Principal Investigator)

    1/04/2331/03/28

    Project: Research

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