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Alzheimer Disease Clinical Trials Targeting Amyloid

机译:Alzheimer疾病临床试验靶向淀粉样蛋白

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Background: The goal of slowing or halting the development of Alzheimer disease (AD) has resulted in the huge allocation of resources by academic institutions and pharmaceutical companies to the development of new treatments. The etiology of AD is elusive, but the aggregation of amyloid-β and tau peptide and oxidative processes are considered critical pathologic mechanisms. The failure of drugs with multiple mechanisms to meet efficacy outcomes has caused several companies to decide not to pursue further AD studies and has left the field essentially where it has been for the past 15 years. Efforts are underway to develop biomarkers for detection and monitoring of AD using genetic, imaging, and biochemical technology, but this is of minimal use if no intervention can be offered. Review Summary: In this review, we consider the natural progression of AD and how it continues despite present attempts to modify the amyloid-related machinery to alter the disease trajectory. We describe the mechanisms and approaches to AD treatment targeting amyloid, including both passive and active immunotherapy as well as inhibitors of enzymes in the amyloidogenic pathway. Conclusion: Lessons learned from clinical trials of amyloid reduction strategies may prove crucial for the leap forward toward novel therapeutic targets to treat AD.
机译:背景:减缓或阻止阿尔茨海默病(AD)发展的目标导致学术机构和制药公司为开发新疗法投入了大量资源。AD的病因尚不清楚,但淀粉样β和tau肽的聚集和氧化过程被认为是重要的病理机制。具有多种机制的药物未能达到疗效结果,导致几家公司决定不再进行进一步的AD研究,并使该领域基本上保持了过去15年的水平。目前正在努力利用基因、成像和生化技术开发用于检测和监测AD的生物标志物,但如果不能提供干预,这种方法的作用将微乎其微。审查摘要:在本次审查中,我们考虑AD的自然进展,以及它如何继续,尽管目前试图修改淀粉样蛋白相关的机器,以改变疾病的轨迹。我们描述了针对淀粉样蛋白的AD治疗机制和方法,包括被动和主动免疫治疗以及淀粉样蛋白生成途径中的酶抑制剂。结论:从淀粉样蛋白减少策略的临床试验中获得的经验教训可能证明对于向治疗AD的新治疗目标迈进至关重要。

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