Pedro-Botet Juan, Climent Elisenda, Benaiges David
Endocrinology and Nutrition Department, Hospital del Mar, 08003 Barcelona, Spain.
Department of Medicine, Universitat Autònoma de Barcelona, Campus Universitari Mar, 08003 Barcelona, Spain.
Biomedicines. 2021 Jul 13;9(7):810. doi: 10.3390/biomedicines9070810.
Cardiovascular disease (CVD) in heterozygous familial hypercholesterolemia (HeFH), the most frequent monogenic disorder of human metabolism, is largely driven by low-density lipoprotein (LDL) cholesterol concentrations. Since the CVD rate differs considerably in this population, beyond the lifetime LDL cholesterol vascular accumulation, other classical risk factors are involved in the high cardiovascular risk of HeFH. Among other lipoprotein disturbances, alterations in the phenotype and functionality of high-density lipoproteins (HDL) have been described in HeFH patients, contributing to the presence and severity of CVD. In fact, HDL are the first defensive barrier against the burden of high LDL cholesterol levels owing to their contribution to reverse cholesterol transport as well as their antioxidant and anti-inflammatory properties, among others. In this context, the present narrative review aimed to focus on quantitative and qualitative abnormalities in HDL particles in HeFH, encompassing metabolic, genetic and epigenetic aspects.
心血管疾病(CVD)在杂合子家族性高胆固醇血症(HeFH)中较为常见,这是人类代谢中最常见的单基因疾病,主要由低密度脂蛋白(LDL)胆固醇浓度驱动。由于该人群的心血管疾病发生率差异很大,除了终生LDL胆固醇在血管中的积累外,其他经典危险因素也与HeFH的高心血管风险有关。在其他脂蛋白紊乱中,HeFH患者已被描述有高密度脂蛋白(HDL)的表型和功能改变,这导致了心血管疾病的发生和严重程度。事实上,HDL是抵御高LDL胆固醇水平负担的第一道防御屏障,这归因于它们对胆固醇逆向转运的贡献以及它们的抗氧化和抗炎特性等。在此背景下,本叙述性综述旨在关注HeFH中HDL颗粒的定量和定性异常,包括代谢、遗传和表观遗传方面。