Evidence for changing lipid management strategy to focus on non-high density lipoprotein cholesterol
Open accessAbstract
Low-density lipoprotein cholesterol (LDL-C) has been recommended as the primary treatment target on lipid management in coronary heart disease (CHD) patients for past several decades. However, even by aggressive LDL-C lowering treatment, patients still present a significant residual risk of major adverse cardiovascular events (MACE). Non-high-density lipoprotein cholesterol (non-HDL-C) contained all the atherogenic lipoproteins, such as chylomicron, very-low density lipoprotein (VLDL), LDL, intermediate density lipoprotein (IDL). Many prospective observation studies have found that non-HDL-C was better than LDL-C in predicting risks of MACE. Since non-HDL-C appears to be superior for risk prediction beyond LDL-C, current guidelines have emphasize the importance of non-HDL-C for guiding cardiovascular prevention strategies and have flagged non-HDL-C as a co-primary therapeutic target. The goals of non-HDL-C were recommended as 30 mg/dl higher than the corresponding LDL-C goals, but the value seemed inappropriate. This review provide evidence for changing lipid management strategy to focus on non-HDL-C and appropriate values for adding to LDL-C goals would be proposed.
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A decrease in atherogenic lipoproteins and sub-fractions is associated with a similar reduction in coronary heart disease.
“Such a decrease in atherogenic lipoproteins and sub-fractions is also associated with a similar reduction in coronary heart disease [105–107].”
From Estimating the Effect of Aerobic Exercise Training on Novel Lipid Biomarkers: A Systematic Review and Multivariate Meta-Analysis of Randomized Controlled Trials (2023) · cites this paper as [106]
The ‘Non-HDL-C as a better target of lipid-lowering therapy’ section reports an approximately one-to-one relationship between percentage non-HDL-C lowering and CHD reduction for most lipid-modifying drugs used alone. The Introduction says non-HDL-C encompasses multiple atherogenic lipoproteins, but the reported relationship concerns their combined measure, not reductions in each lipoprotein sub-fraction separately. Page numbers are unavailable in our copy. (LLM, conf=0.82)
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Wood, G., Taylor, E., Ng, V., Murrell, A., Patil, A., van der Touw, T., Wolden, M., Andronicos, N., & Smart, N. A. (2023) · Sports Medicine · doi:10.1007/s40279-023-01817-0 · Cited by 31 · see citing works
- Authors
- Su, X., Kong, Y., & Peng, D.
- Affiliations
- Second Xiangya Hospital of Central South University (CN)
- Central South University (CN)
- Corresponding author
- Peng, Daoquan
- ORCID
- Venue
- Lipids in Health and Disease
- Published
- 2019-06-07
- Volume
- 18
- Issue
- 1
- Pages
- 134-134
- ISSN
- 1476-511X (ISSN-L)
- PMC
- PMC6554877
- OpenAlex
- W2948745207
- Cited by
- 72
- References
- 11
- Citations by year
- 2026: 3 · 2025: 8 · 2024: 10 · 2023: 10 · 2022: 14 · 2021: 13 · 2020: 12 · 2019: 2
- FWCI
- 2.11
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Lipids in Health and Disease (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Natural Science Foundation of China (81670426, 81870336)
- Topics
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Keywords
- non-HDL cholesterol, LDL cholesterol, lipid control, coronary artery disease, major adverse cardiovascular events, residual cardiovascular risk, atherogenic lipoproteins, cardiovascular risk prediction
- MeSH terms
- Cardiovascular Diseases, Chylomicrons, Coronary Disease, Humans, Lipids, Cholesterol, HDL, Cholesterol, LDL, Risk Factors, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Lipid Metabolism, Drug-Related Side Effects and Adverse Reactions
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