小胶质细胞
淀粉样蛋白(真菌学)
疾病
阿尔茨海默病的生物化学
淀粉样β
阿尔茨海默病
认知功能衰退
生物
神经科学
临床试验
淀粉样前体蛋白
痴呆
生物信息学
医学
病理
免疫学
炎症
作者
Christian Haass,Dennis J. Selkoe
出处
期刊:PLOS Biology
[Public Library of Science]
日期:2022-07-21
卷期号:20 (7): e3001694-e3001694
被引量:96
标识
DOI:10.1371/journal.pbio.3001694
摘要
Strong genetic evidence supports an imbalance between production and clearance of amyloid β-protein (Aβ) in people with Alzheimer disease (AD). Microglia that are potentially involved in alternative mechanisms are actually integral to the amyloid cascade. Fluid biomarkers and brain imaging place accumulation of Aβ at the beginning of molecular and clinical changes in the disease. So why have clinical trials of anti-amyloid therapies not provided clear-cut benefits to patients with AD? Can anti-amyloid therapies robustly decrease Aβ in the human brain, and if so, could this lowering be too little, too late? These central questions in research on AD are being urgently addressed.
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