Neuroinflammation in Alzheimer's disease: Current evidence and future directions

被引:1206
作者
Calsolaro, Valeria [1 ]
Edison, Paul [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Neurol Imaging Unit, London SW7 2AZ, England
基金
英国医学研究理事会;
关键词
Alzheimer's; Microglia; Neuroinflammation; Neurodegeneration; Systemic inflammation; PET; RANDOMIZED CONTROLLED-TRIAL; MILD COGNITIVE IMPAIRMENT; AMYLOID PRECURSOR PROTEIN; POSITRON-EMISSION-TOMOGRAPHY; PERIPHERAL BENZODIAZEPINE-RECEPTOR; MICROGLIAL ACTIVATION; SYSTEMIC INFLAMMATION; CHRONIC NEURODEGENERATION; DOUBLE-BLIND; PARKINSONS-DISEASE;
D O I
10.1016/j.jalz.2016.02.010
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Several attempts have been made to treat Alzheimer's disease (AD) using anti-amyloid strategies with disappointing results. It is clear that the "amyloid cascade hypothesis" alone cannot fully explain the neuronal damage in AD, as evidenced both by autopsy and imaging studies. Neuroinflammation plays a significant role in neurodegenerative diseases, whereas the debate is ongoing about its precise role, whether it is protective or harmful. In this review, we focus on the potential mechanism of glial activation and how local and systemic factors influence disease progression. We focus on neuroinflammation in AD, especially in the earliest stages, a vicious cycle of glial priming, release of proinflammatory factors, and neuronal damage. We review the evidence from imaging studies, regarding the temporal relationship between amyloid deposition and neuroinflammation, the influence of systemic inflammation on glial activation, both in acute and chronic stimulation and the relevance of inflammation as a diagnostic and therapeutic target. (C) 2016 The Alzheimer's Association. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:719 / 732
页数:14
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