Abstract

In the general population, the ability of high-density lipoproteins (HDLs) to promote cholesterol efflux is a predictor of cardiovascular events, independently of HDL cholesterol levels. Although patients with chronic kidney disease (CKD) have a high burden of cardiovascular morbidity and mortality, neither serum levels of HDL cholesterol, nor cholesterol efflux capacity associate with cardiovascular events. Important for the following discussion on the role of HDL in CKD is the notion that traditional atherosclerotic cardiovascular risk factors only partially account for this increased incidence of cardiovascular disease in CKD. As a potential explanation, across the spectrum of cardiovascular disease, the relative contribution of atherosclerotic cardiovascular disease becomes less important with advanced CKD. Impaired renal function directly affects the metabolism, composition and functionality of HDL particles. HDLs themselves are a heterogeneous population of particles with distinct sizes and protein composition, all of them affecting the functionality of HDL. Therefore, a more specific approach investigating the functional and compositional features of HDL subclasses might be a valuable strategy to decipher the potential link between HDL, cardiovascular disease and CKD. This review summarizes the current understanding of the relationship of HDL composition, metabolism and function to their cardio-protective properties in CKD, with a focus on CKD-induced changes in the HDL proteome and reverse cholesterol transport capacity. We also will highlight the gaps in the current knowledge regarding important aspects of HDL biology.

Highlights

  • High-density lipoprotein (HDL) cholesterol (HDL-C) is inversely associated with the risk of atherosclerotic cardiovascular disease (ASCVD) and is a key component in predicting cardiovascular risk in the general population [1]

  • One hypothesis is that in individuals with extremely high HDL-C, the functional properties of HDL are altered/impaired so that HDL no longer functions normally but is more likely to cause harm. Another hypothesis is that free cholesterol transfer to HDL upon lipolysis of triglyceride-rich lipoproteins may underlie the U-shaped relationship between HDL-C and cardiovascular disease, linking HDL-C to triglyceride metabolism and atherosclerosis [37]

  • One study among renal allograft recipients reported that cholesterol efflux capacity strongly predicted kidney graft failure independent of plasma HDL-C levels [131]

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Summary

Introduction

High-density lipoprotein (HDL) cholesterol (HDL-C) is inversely associated with the risk of atherosclerotic cardiovascular disease (ASCVD) and is a key component in predicting cardiovascular risk in the general population [1]. The contribution of classical atherosclerotic risk factors to the development of cardiovascular disease is less evident in patients with advanced CKD compared to patients with intact kidney function, while non-classical risk factors become more important [3]. This becomes clear when one considers the lipid metabolism: Uremic dyslipidemia is characterized by hypertriglyceridemia and low HDL-C levels, whereas patients with advanced CKD rarely have elevated low-density lipoprotein cholesterol (LDL-C) levels [4]. In contrast to myocardial infarction and stroke, which are central events of atherosclerotic cardiovascular disease, these non-atherosclerotic vascular and cardiac pathologies are less consistently mediated by atherosclerotic risk factors, as described below

CKD-Associated High Cardiovascular Risk
What is the Physiological Function of HDL?
HDL Biosynthesis and Remodeling
HDL Structure and Composition
HDL Subclasses
CKD Profoundly Changes HDL Maturation and Metabolism
CKD-Associated Changes in HDL Subclasses Distribution
Method Native gel electrophoresis
CKD-Induced Changes in the HDL Proteome
Isolation Method
HDL-Cholesterol Efflux Capacity in CKD Patients
CKD-Associated Changes of Other HDL Functions
Findings
Conclusions
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