Center for Innovation in Brain Science, University of Arizona Health Sciences, Tucson, AZ, USA.
Department of Pharmacology, College of Medicine Tucson, University of Arizona, Tucson, AZ, USA.
FEBS J. 2023 Mar;290(6):1420-1453. doi: 10.1111/febs.16344. Epub 2022 Jan 18.
Alzheimer's disease (AD) is an age-associated neurodegenerative disorder with multifactorial etiology, intersecting genetic and environmental risk factors, and a lack of disease-modifying therapeutics. While the abnormal accumulation of lipids was described in the very first report of AD neuropathology, it was not until recent decades that lipid dyshomeostasis became a focus of AD research. Clinically, lipidomic and metabolomic studies have consistently shown alterations in the levels of various lipid classes emerging in early stages of AD brains. Mechanistically, decades of discovery research have revealed multifaceted interactions between lipid metabolism and key AD pathogenic mechanisms including amyloidogenesis, bioenergetic deficit, oxidative stress, neuroinflammation, and myelin degeneration. In the present review, converging evidence defining lipid dyshomeostasis in AD is summarized, followed by discussions on mechanisms by which lipid metabolism contributes to pathogenesis and modifies disease risk. Furthermore, lipid-targeting therapeutic strategies, and the modification of their efficacy by disease stage, ApoE status, and metabolic and vascular profiles, are reviewed.
阿尔茨海默病(AD)是一种与年龄相关的神经退行性疾病,具有多因素病因,涉及遗传和环境风险因素的交叉,并且缺乏可改变疾病进程的治疗方法。虽然在 AD 神经病理学的第一篇报告中就描述了脂质的异常积累,但直到最近几十年,脂质代谢失衡才成为 AD 研究的重点。临床上,脂质组学和代谢组学研究一致表明,在 AD 大脑的早期阶段,各种脂质类别的水平发生了改变。从机制上讲,数十年的发现研究揭示了脂质代谢与包括淀粉样蛋白形成、生物能量不足、氧化应激、神经炎症和髓鞘退化在内的关键 AD 发病机制之间的多方面相互作用。在本综述中,总结了定义 AD 中脂质代谢失衡的综合证据,并讨论了脂质代谢对发病机制的贡献以及改变疾病风险的机制。此外,还综述了针对脂质的治疗策略,以及疾病阶段、ApoE 状态、代谢和血管特征对其疗效的修饰。