Emerging drug targets for A and tau in Alzheimer's disease: a systematic review

被引:34
|
作者
West, Sophie [1 ]
Bhugra, Praveen [1 ]
机构
[1] Univ Sunderland, Dept Pharm Hlth & Wellbeing, Sunderland Pharm Sch, Sunderland SR1 3SD, Durham, England
关键词
Alzheimer's disease; A beta; emerging targets; systematic review; tau; MOUSE MODEL; A-BETA; COGNITIVE IMPAIRMENT; MEMORY DEFICITS; TRANSGENIC MICE; IN-VITRO; PROTEIN; HYPERPHOSPHORYLATION; INVOLVEMENT; INHIBITION;
D O I
10.1111/bcp.12621
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
AimsCurrently, treatment for Alzheimer's disease (AD) focuses on the cholinergic hypothesis and provides limited symptomatic effects. Research currently focuses on other factors that are thought to contribute to AD development such as tau proteins and A deposits, and how modification of the associated pathology affects outcomes in patients. This systematic review summarizes and appraises the evidence for the emerging drugs affecting A and tau pathology in AD. MethodsA comprehensive, systematic online database search was conducted using the databases ScienceDirect and PubMed to include original research articles. A systematic review was conducted following a minimum set of standards, as outlined by The PRISMA Group . Specific inclusion and exclusion criteria were followed and studies fitting the criteria were selected. No human trials were included in this review. In vitro and in vivo AD models were used to assess efficacy to ensure studied agents were emerging targets without large bodies of evidence. ResultsThe majority of studies showed statistically significant improvement (P < 0.05) of A and/or tau pathology, or cognitive effects. Many studies conducted in AD animal models have shown a reduction in A peptide burden and a reduction in tau phosphorylation post-intervention. This has the potential to reduce plaque formation and neuronal degeneration. ConclusionsThere are many emerging targets showing promising results in the effort to modify the pathological effects associated with AD. Many of the trials also provided evidence of the clinical effects of such drugs reducing pathological outcomes, which was often demonstrated as an improvement of cognition.
引用
收藏
页码:221 / 234
页数:14
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