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Assessing Whole-Body Lipid-Handling Capacity in Mice
Published on: November 24, 2020
Hypertriglyceridaemia, postprandial lipaemia and non-HDL cholesterol
Claudia Stefanutti, Giancarlo Labbadia, Vasilios G Athyros1
1Extracorporeal Therapeutic Techniques - Lipid Clinic and Atherosclerosis Prevention Centre - Immunohematology and Transfusion Medicine - Department of Molecular Medicine, University of Rome "Sapienza" - Umberto I Hospital-155, Viale del Policlinico, Rome, 00161, Italy (EU). claudia.stefanutti@uniroma1.it.
Maintaining healthy lipid levels like triglycerides (TG) and high-density lipoprotein cholesterol (HDL-C) is crucial for cardiovascular health. This review explores the complex relationship between TG, postprandial lipemia, and cardiovascular disease risk.
Area of Science:
- Cardiovascular Science
- Lipid Metabolism
- Atherosclerosis Research
Background:
- Elevated total cholesterol (TC), LDL-C, HDL-C, and TG are linked to atherosclerotic vascular disease (AVD) and cardiovascular (CV) events.
- The predictive value of high TG for coronary artery disease (CAD) diminishes in multivariate analyses, particularly after adjusting for HDL-C.
- The intricate relationship between TG and HDL-C, influenced by factors like postprandial lipemia (PPL), remains incompletely understood.
Purpose of the Study:
- To review the complex interplay between triglycerides (TG), postprandial lipemia (PPL), and postprandial hyperlipidemia.
- To examine the potential role of these factors in atherogenesis and cardiovascular disease (CVD).
- To discuss the implications for cardiovascular risk assessment, considering fasting versus non-fasting lipid measurements.
Main Methods:
- Literature review focusing on TG, PPL, postprandial hyperlipidemia, and non-HDL-C.
- Analysis of the relationship between these lipid parameters and their predictive value for CVD.
- Examination of lipoprotein heterogeneity and its impact on atherogenicity.
Main Results:
- Hydrolysis of TG by lipoprotein lipase alters HDL subclasses during PPL.
- TG-transporting lipoproteins (chylomicrons, VLDL, remnants) are heterogeneous and may vary in atherogenicity.
- Alterations in lipoprotein concentration and composition during PPL, termed "postprandial hyperlipidemia," may contribute to CVD development.
Conclusions:
- The relationship between TG, HDL-C, and PPL is complex and significant for understanding CVD risk.
- Current CVD risk assessment relies on fasting lipid levels, potentially overlooking the impact of postprandial changes.
- Further research into TG metabolism during PPL and its atherogenic potential is warranted for improved risk prediction.
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