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阿尔茨海默病治疗和预防策略的最新进展。

Update on Alzheimer's Disease Therapy and Prevention Strategies.

机构信息

Laboratory of Chemical Biology and Signal Transduction, The Rockefeller University, New York, NY 10065; email:

Department of Neurobiology, Care Sciences and Society, Center for Alzheimer Research, Division of Neurogeriatrics, Karolinska Institutet, 141 57 Huddinge, Sweden.

出版信息

Annu Rev Med. 2017 Jan 14;68:413-430. doi: 10.1146/annurev-med-042915-103753.

Abstract

Alzheimer's disease (AD) is the primary cause of age-related dementia. Effective strategies to prevent and treat AD remain elusive despite major efforts to understand its basic biology and clinical pathophysiology. Significant investments in therapeutic drug discovery programs over the past two decades have yielded some important insights but no blockbuster drugs to alter the course of disease. Because significant memory loss and cognitive decline are associated with neuron death and loss of gray matter, especially in the frontal cortex and hippocampus, some focus in drug development has shifted to early prevention of cellular pathology. Although clinical trial design is challenging, due in part to a lack of robust biomarkers with predictive value, some optimism has come from the identification and study of inherited forms of early-onset AD and genetic risk factors that provide insights about molecular pathophysiology and potential drug targets. In addition, better understanding of the Aβ amyloid pathway and the tau pathway-leading to amyloid plaques and neurofibrillary tangles, respectively, which are histopathological hallmarks of AD-continues to drive significant drug research and development programs. The main focus of this review is to summarize the most recent basic biology, biochemistry, and pharmacology that serve as a foundation for more than 50 active advanced-phase clinical trials for AD prevention and therapy.

摘要

阿尔茨海默病(AD)是与年龄相关的痴呆的主要病因。尽管人们为了解其基础生物学和临床病理生理学做出了巨大努力,但仍未找到有效的预防和治疗 AD 的策略。在过去的二十年中,在治疗药物研发计划上进行了大量投资,虽然取得了一些重要的见解,但仍未研发出能够改变疾病进程的重磅药物。由于与神经元死亡和灰质丧失有关的显著记忆丧失和认知能力下降,特别是在额叶皮层和海马体中,药物研发的一些重点已转移到早期预防细胞病理学。尽管临床试验设计具有挑战性,部分原因是缺乏具有预测价值的强大生物标志物,但从鉴定和研究早发性 AD 的遗传形式以及遗传风险因素中获得了一些乐观的结果,这些遗传风险因素提供了有关分子病理生理学和潜在药物靶点的见解。此外,对 Aβ 淀粉样蛋白途径和 tau 途径(分别导致淀粉样斑块和神经原纤维缠结,这是 AD 的组织病理学标志)的更好理解,继续推动着大量药物研发计划。本综述的主要重点是总结最近的基础生物学、生物化学和药理学,为 50 多项针对 AD 预防和治疗的活跃的高级临床试验奠定了基础。

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