a Institute for NanoBiotechnology , Johns Hopkins University , Baltimore , Maryland , USA.
b King's College London , Wolfson Centre for Age-Related Diseases , London , UK.
Expert Rev Neurother. 2017 Jul;17(7):683-695. doi: 10.1080/14737175.2017.1326818. Epub 2017 May 18.
The number of people with dementia, including Alzheimer's disease, is growing as a result of an ageing global population. Treatments available for AD only alleviate the symptoms of the disease, and are effective in some people with AD for a limited time. There is no disease-modifying treatment available, and despite research efforts, the underlying mechanisms of AD and optimal treatment targets have not been fully elucidated. Amyloid and tau are key pathological markers of AD with ongoing trials targeting both. However, there are also many trials at various stages of development that primarily target other markers and processes implicated in the disease, which are now being investigated. Areas covered: This review summarizes current treatment approaches for AD and explores both repositioned and novel therapies that target non amyloid and non tau mechanisms that are in the clinical trials pipeline. This includes treatments for cognitive and neuropsychiatric symptoms and potentially disease modifying therapies. The studies included in this review have been obtained from searches of PubMed and clinical trials databases. Expert commentary: There is a renewed energy in identifying better treatments for behavioural symptoms of AD using both novel drugs and repositioning existing drugs. Lack of success in clinical trials of drugs targeting amyloid and tau have led to a surge in targeting alternative mechanisms. Progress in the development of biomarkers will provide further tools for clinical trials of potential therapeutics for both symptomatic treatment and disease modification in AD.
随着全球人口老龄化,痴呆症(包括阿尔茨海默病)患者的数量不断增加。目前可用于治疗 AD 的方法只能缓解疾病的症状,并且在有限的时间内对某些 AD 患者有效。目前尚无针对疾病的治疗方法,尽管进行了研究,但 AD 的潜在机制和最佳治疗靶点尚未完全阐明。淀粉样蛋白和 tau 是 AD 的关键病理标志物,目前正在进行针对这两者的临床试验。然而,还有许多处于不同开发阶段的临床试验主要针对疾病相关的其他标志物和过程,目前正在对此进行研究。涵盖领域:本综述总结了目前 AD 的治疗方法,并探讨了处于临床试验阶段的针对非淀粉样蛋白和非 tau 机制的重新定位和新型疗法。这包括针对认知和神经精神症状的治疗方法以及潜在的疾病修正治疗方法。本综述中包含的研究是通过在 PubMed 和临床试验数据库中搜索获得的。专家评论:使用新型药物和重新定位现有药物来确定治疗 AD 行为症状的更好方法的新活力。针对淀粉样蛋白和 tau 的药物临床试验的失败导致针对替代机制的药物临床试验数量激增。生物标志物的开发进展将为 AD 的潜在治疗药物的临床试验提供进一步的工具,包括症状治疗和疾病修饰。
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