Huang Yihong, Tang Jingyi, Chen Guohua, Wu Qiangqiang, Wang Yongfei, Chen Jianjun, Chen Simei, Liu Jun, Huang Xiaoyun
Department of Neurology Houjie Hospital and Clinical College of Guangdong Medical University Dongguan Guangdong China.
Department of Neurology Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University Guangzhou Guangdong China.
Aging Med (Milton). 2025 Mar 20;8(2):164-177. doi: 10.1002/agm2.70008. eCollection 2025 Apr.
High-density lipoprotein (HDL), as a crucial component of lipid metabolism, have roles in regulating Alzheimer's disease (AD) core pathology amyloid β (Aβ) and phosphorylated tau (p-tau) through its apolipoproteins, which are associated with brain structures, cognition, and risk of dementia. The pool of HDL apolipoproteins-in the brain and in the periphery-has its own distinct origin, composition, and regulatory mechanisms. It remains unclear whether these apolipoproteins in the periphery and CNS play distinct roles in the pathogenesis of AD. Specifically, this review focus on the distinct associations of apolipoprotein AI and apolipoprotein E-the major components of HDL in the blood and CSF-with pathological proteins, brain integrity, cognition, and dementia progression in AD. We summarize and examine the current state of knowledge on the values of these apolipoproteins in AD pathogenesis and clinical potential.
高密度脂蛋白(HDL)作为脂质代谢的关键组成部分,通过其载脂蛋白在调节阿尔茨海默病(AD)的核心病理淀粉样β蛋白(Aβ)和磷酸化tau蛋白(p-tau)方面发挥作用,这些载脂蛋白与脑结构、认知及痴呆风险相关。脑内和外周的HDL载脂蛋白库有其独特的来源、组成和调节机制。目前尚不清楚外周和中枢神经系统中的这些载脂蛋白在AD发病机制中是否发挥不同作用。具体而言,本综述聚焦于血液和脑脊液中HDL的主要成分载脂蛋白AI和载脂蛋白E与AD病理蛋白、脑完整性、认知及痴呆进展的不同关联。我们总结并审视了关于这些载脂蛋白在AD发病机制中的价值及临床潜力的现有知识状态。