Amin Jay, Erskine Daniel, Donaghy Paul C, Surendranathan Ajenthan, Swann Peter, Kunicki Amy P, Boche Delphine, Holmes Clive, McKeith Ian G, O'Brien John T, Teeling Jessica L, Thomas Alan J
Clinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, UK; Memory Assessment and Research Centre, Southern Health NHS Foundation Trust, Southampton, UK..
Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, UK.
Neurobiol Dis. 2022 Jun 15;168:105698. doi: 10.1016/j.nbd.2022.105698. Epub 2022 Mar 18.
Dementia with Lewy bodies (DLB) is the second most common neurodegenerative cause of dementia, behind Alzheimer's disease (AD). The profile of inflammation in AD has been extensively researched in recent years, with evidence that chronic peripheral inflammation in midlife increases the risk of late-onset AD, and data supporting inflammation being associated with disease progression. In contrast, our understanding of the role of inflammation in DLB is less developed. Most research to date has examined inflammation in related disorders, such as Parkinson's disease, but there is now a growing range of literature examining inflammation in DLB itself. We present a review of the literature in this field, exploring a range of research methodologies including those quantifying markers of inflammation in cerebrospinal fluid, peripheral blood, post-mortem brain tissue, and using neuroimaging and preclinical data. Our review reveals evidence from PET imaging and peripheral blood analysis to support an increase in cerebral and peripheral inflammation in mild or prodromal DLB, that dissipates with disease progression. We present evidence from post-mortem brain tissue and pre-clinical studies that indicate α-synuclein directly promotes inflammation, but that also support the presence of AD co-pathology as an important factor in the profile of neuroinflammation in DLB. We propose that specific markers of inflammation may play a sentinel role in the mild stage of the disease, particularly when combined with AD pathology. We advocate further examination of the profile of inflammation in DLB through robust longitudinal studies, to enhance our understanding of the pathogenesis of the disease. The goal should be to utilise future results to develop a composite biomarker to aid diagnosis of DLB, and to potentially identify novel therapeutic targets.
路易体痴呆(DLB)是仅次于阿尔茨海默病(AD)的第二常见的神经退行性痴呆病因。近年来,AD中的炎症特征已得到广泛研究,有证据表明中年时期的慢性外周炎症会增加晚发性AD的风险,并且有数据支持炎症与疾病进展相关。相比之下,我们对炎症在DLB中的作用的了解较少。迄今为止,大多数研究都考察了相关疾病(如帕金森病)中的炎症,但现在越来越多的文献开始研究DLB本身的炎症。我们对该领域的文献进行了综述,探讨了一系列研究方法,包括那些量化脑脊液、外周血、死后脑组织中的炎症标志物的方法,以及使用神经影像学和临床前数据的方法。我们的综述揭示了来自PET成像和外周血分析的证据,支持在轻度或前驱性DLB中脑和外周炎症增加,且这种炎症会随着疾病进展而消散。我们展示了来自死后脑组织和临床前研究的证据,这些证据表明α-突触核蛋白直接促进炎症,但也支持AD共病病理作为DLB神经炎症特征中的一个重要因素的存在。我们提出,炎症的特定标志物可能在疾病的轻度阶段发挥哨兵作用,特别是当与AD病理相结合时。我们主张通过有力的纵向研究进一步考察DLB中的炎症特征,以增进我们对该疾病发病机制的理解。目标应该是利用未来的研究结果开发一种复合生物标志物,以辅助DLB的诊断,并有可能识别新的治疗靶点。