Qi Xiaoming, Nizamutdinov Damir, Yi Song Stephen, Wu Erxi, Huang Jason H
Department of Neurology, Baylor Scott & White Health, Temple, TX 78508, USA.
Department of Neurosurgery, Neuroscience Institute, Baylor Scott & White Health, Temple, TX 78508, USA.
Biomedicines. 2024 Nov 19;12(11):2636. doi: 10.3390/biomedicines12112636.
Alzheimer's Disease (AD) is an irreversible, progressive syndrome characterized by neurocognitive impairment. Two neuropathological features seen in AD are extracellular amyloid plaques consisting of amyloid beta1-40 and 1-42, and intracellular neurofibrillary tangles (NFTs). For decades, neuroscience research has heavily focused on seeking to understand the primary mechanism of AD and searching for pharmacological approaches for the treatment of dementia. Three monoclonal antibodies that act against amyloid beta-aducanumab, lecanemab, and donanemab-have been approved by the Food and Drug Administration (FDA) for the treatment of mild cognitive impairment and mild AD, in addition to medications for cognitive symptom management such as acetylcholinesterase inhibitors and the N-methyl-D-aspartate (NMDA) antagonist. Further trials should focus on the combination of therapies targeting amyloid plaques and tau pathology.
阿尔茨海默病(AD)是一种以神经认知障碍为特征的不可逆的进行性综合征。AD中可见的两种神经病理学特征是由β淀粉样蛋白1-40和1-42组成的细胞外淀粉样斑块,以及细胞内神经原纤维缠结(NFTs)。几十年来,神经科学研究主要集中在试图了解AD的主要机制以及寻找治疗痴呆症的药理学方法。三种抗β淀粉样蛋白的单克隆抗体——阿杜卡单抗、乐卡奈单抗和多奈单抗——已被美国食品药品监督管理局(FDA)批准用于治疗轻度认知障碍和轻度AD,此外还有用于管理认知症状的药物,如乙酰胆碱酯酶抑制剂和N-甲基-D-天冬氨酸(NMDA)拮抗剂。进一步的试验应侧重于针对淀粉样斑块和tau病理的联合治疗。