医学
疾病
生物信息学
淀粉样蛋白(真菌学)
神经科学
重症监护医学
阿尔茨海默病
药品
淀粉样β
认知功能衰退
病态的
药物开发
竞争对手
药物发现
痴呆
胰岛素
病理生理学
动作(物理)
报销
药理学
治疗方法
神经影像学
β淀粉样蛋白
作用机理
药物治疗
生活质量(医疗保健)
认知
药物治疗
机制(生物学)
糖尿病
作者
Joseph Nowell,Harry Crook,Mony J. de Leon,Paul Edison
出处
期刊:
日期:2026-04-20
卷期号:393: bmj-2023
被引量:2
标识
DOI:10.1136/bmj-2023-078881
摘要
Alzheimer's disease, the leading cause of dementia, is a multifactorial disorder involving amyloid beta (Aβ) and tau deposition, impaired glucose metabolism, neuroinflammation, mitochondrial dysfunction, insulin resistance, and progressive brain atrophy. Anti-Aβ therapies have shown clinical efficacy and are licensed in several countries. Amyloid related imaging abnormalities remain a key safety concern, and reimbursement varies across healthcare systems. The mechanisms underlying continued cognitive decline after Aβ clearance remain unclear and might be independent of amyloid pathology. Because Alzheimer's disease involves multiple pathological processes, effective management will likely require combination treatments addressing tau aggregation, neuroinflammation, synaptic loss, and metabolic dysfunction. Numerous compounds targeting these mechanisms are currently in late stage development for both early and advanced disease. These emerging approaches represent a shift toward multimodal, disease modifying strategies designed to improve patient outcomes and quality of life. Here, we review recent therapeutic advances in Alzheimer's disease and provide perspectives on novel treatment strategies.
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