Disease-Modifying Therapies for Alzheimer's Disease: More Questions than Answers

被引:80
作者
Golde, Todd E. [1 ]
机构
[1] Univ Florida, Evelyn F & William L McKnight Brain Inst, Ctr Translat Res Neurodegenerat Dis, Norman Fixel Inst Neurol Dis,Dept Neurosci & Neur, Gainesville, FL 32611 USA
关键词
Alzheimer's disease; Therapeutics; Amyloid; Tau; Inflammation; Prevention; Disease modification; BETA IMMUNIZATION AN1792; O-GLCNACASE INHIBITOR; AMYLOID-BETA; MOUSE MODEL; PATHOLOGICAL TAU; DOUBLE-BLIND; NEUROFIBRILLARY DEGENERATION; CEREBROSPINAL-FLUID; FUNCTIONAL DECLINE; DRUG DEVELOPMENT;
D O I
10.1007/s13311-022-01201-2
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Scientific advances over the last four decades have steadily infused the Alzheimer's disease (AD) field with great optimism that therapies targeting A beta, amyloid, tau, and innate immune activation states in the brain would provide disease modification. Unfortunately, this optimistic scenario has not yet played out. Though a recent approval of the anti-A beta aggregate binding antibody, Aduhelm (aducanumab), as a "disease-modifying therapy for AD" is viewed by some as a breakthrough, many remain unconvinced by the data underlying this approval. Collectively, we have not succeeded in changing AD from a largely untreatable, inevitable, and incurable disease to a treatable, preventable, and curable one. Here, I will review the major foci of the AD "disease-modifying" therapeutic pipeline and some of the "open questions" that remain in terms of these therapeutic approaches. I will conclude the review by discussing how we, as a field, might adjust our approach, learning from our past failures to ensure future success.
引用
收藏
页码:209 / 227
页数:19
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