Advances in developing novel therapeutic strategies for Alzheimer's disease

被引:203
作者
Cao, Jiqing [1 ,2 ,3 ]
Hou, Jianwei [1 ,2 ]
Ping, Jing [3 ]
Cai, Dongming [1 ,2 ,3 ]
机构
[1] James J Peters VA Med Ctr, Res & Dev, Bronx, NY 10468 USA
[2] Icahn Sch Med Mt Sinai, Alzheimer Dis Res Ctr, Dept Neurol, New York, NY 10029 USA
[3] Hua Zhong Univ Sci & Technol, Cent Hosp, Wuhan, Hubei, Peoples R China
关键词
Alzheimer's disease; Novel therapies; Pre-clinical and clinical trials; Drug development; NERVE GROWTH-FACTOR; TRANSGENIC MOUSE MODEL; E/AMYLOID-BETA INTERACTION; AGGREGATION INHIBITOR THERAPY; MILD COGNITIVE IMPAIRMENT; APOLIPOPROTEIN-E GENOTYPE; GAMMA-SECRETASE ACTIVITY; PREVENTS SYNAPTIC LOSS; FACTOR GENE-THERAPY; II CLINICAL-TRIALS;
D O I
10.1186/s13024-018-0299-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's Disease (AD), the most prevalent neurodegenerative disease of aging, affects one in eight older Americans. Nearly all drug treatments tested for AD today have failed to show any efficacy. There is a great need for therapies to prevent and/or slow the progression of AD. The major challenge in AD drug development is lack of clarity about the mechanisms underlying AD pathogenesis and pathophysiology. Several studies support the notion that AD is a multifactorial disease. While there is abundant evidence that amyloid plays a role in AD pathogenesis, other mechanisms have been implicated in AD such as tangle formation and spread, dysregulated protein degradation pathways, neuroinflammation, and loss of support by neurotrophic factors. Therefore, current paradigms of AD drug design have been shifted from single target approach (primarily amyloid-centric) to developing drugs targeted at multiple disease aspects, and from treating AD at later stages of disease progression to focusing on preventive strategies at early stages of disease development. Here, we summarize current strategies and new trends of AD drug development, including pre-clinical and clinical trials that target different aspects of disease (mechanism-based versus non-mechanism based, e.g. symptomatic treatments, lifestyle modifications and risk factor management).
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页数:20
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