萎缩
淀粉样蛋白(真菌学)
淀粉样β
医学
病理
免疫疗法
疾病
β淀粉样蛋白
阿尔茨海默病
神经科学
心理学
免疫学
免疫系统
作者
Christopher R S Belder,Delphine Boche,James A. R. Nicoll,Zane Jaunmuktane,Henrik Zetterberg,Jonathan M. Schott,Frederik Barkhof,Nick C. Fox
标识
DOI:10.1016/s1474-4422(24)00335-1
摘要
Progressive cerebral volume loss on MRI is a hallmark of Alzheimer's disease and has been widely used as an outcome measure in clinical trials, with the prediction that disease-modifying treatments would slow loss. However, in trials of anti-amyloid immunotherapy, the participants who received treatment had excess volume loss. Explanations for this observation range from reduction of amyloid β plaque burden and related inflammatory changes through to treatment-induced toxicity. The excess volume changes are characteristic of only those immunotherapies that achieve amyloid β lowering; are compatible with plaque removal; and evidence to date does not suggest an association with harmful effects. Based on the current evidence, we suggest that these changes can be described as amyloid-removal-related pseudo-atrophy. Better understanding of the causes and consequences of these changes is important to enable informed decisions about treatments. Patient-level analyses of data from the trials are urgently needed, along with longitudinal follow-up and neuroimaging data, to determine the long-term trajectory of these volume changes and their clinical correlates. Post-mortem examination of cerebral tissue from treated patients and evaluation of potential correlation with antemortem neuroimaging findings are key priorities.
科研通智能强力驱动
Strongly Powered by AbleSci AI