New Therapeutic Targets in Alzheimer's Disease

被引:46
|
作者
Coman, Horia [1 ]
Nemes, Bogdan [1 ]
机构
[1] Iuliu Hatieganu Univ Med & Pharm Cluj Napoca, Dept Med Psychol, 43rd V Babes St, Cluj Napoca 400012, Romania
关键词
Alzheimer disease; amyloid; tau proteins; GLYCOGEN-SYNTHASE KINASE-3; GAMMA-SECRETASE; CLINICAL-TRIALS; SAFETY; IMMUNOTHERAPY; TOLERABILITY; INHIBITORS; MODERATE; TARENFLURBIL; MEMANTINE;
D O I
10.1016/j.ijge.2016.07.003
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Up to the present, the identification of neurochemical alterations underlying Alzheimer's disease allowed for the development of the first generation of therapies that are somewhat specific for this disorder. Although both cholinesterase inhibitors and NMDA receptor blockade have well-proven efficacy levels, the clinical outcomes of patients receiving such treatments are rather limited; with many authors considering them as "symptomatic" treatments. In this context, it is safe to say that although the microscopic alterations present in AD have been well known for over a century, we have failed to identify therapeutic agents able to block the synthesis and aggregation of amyloid beta 42 or the formation of neurofibrillary tangles. Some new therapeutic strategies have however been explored in the last few years. This paper aimed at reviewing the evidence supporting these new "disease modifying" therapeutic options, including anti-amyloid and anti-Tau strategies. Copyright (C) 2017, Taiwan Society of Geriatric Emergency & Critical Care Medicine. Published by Elsevier Taiwan LLC.
引用
收藏
页码:2 / 6
页数:5
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