Key Laboratory of Ethnomedicine for Ministry of Education, Center on Translational Neuroscience, College of Life and Environmental Sciences, Minzu University of China, Beijing, China.
Front Immunol. 2018 Sep 19;9:2122. doi: 10.3389/fimmu.2018.02122. eCollection 2018.
It has been suggested that cytokine-mediated inflammation plays a key role for the onset and/or development of neurodegenerative diseases including Alzheimer's disease (AD), Parkinson's disease (PD) and Amyotrophic lateral sclerosis (ALS). However, clinical studies have yielded inconsistent results for the aberrant cytokine levels in circulation of patients with AD, PD, and ALS. Previous studies have used meta-analysis to address the inconsistent data for blood cytokine levels in the patients with AD, PD, and ALS. Here, we performed a systemic review of cerebrospinal fluid inflammatory cytokine data in patients with AD, PD and ALS, and sought to quantitatively summarize the CSF inflammatory cytokine data with a meta-analytical technique. The systematic search from Pubmed and Web of Science identified 71 articles with 2629 patients and 2049 controls for the meta-analysis. Random-effects meta-analysis demonstrated that CSF TGF-β, MCP-1, and YKL-40 levels were significantly elevated in AD patients when compared with controls. In addition, patients with PD had heightened levels of TGF-β1, IL-6, and IL-1β in CSF. Furthermore, G-CSF, IL-2, IL-15, IL-17, MCP-1, MIP-1α, TNF-α, and VEGF levels were significantly increased in patients with ALS as compared with controls. Taken together, these results not only strengthen the clinical evidence that neurodegenerative diseases are accompanied by the increased inflammatory response, but also reveal the unique inflammatory response profile in the central nervous system of patients with AD, PD and ALS. Given the robust associations between some cytokines and neurodegenerative diseases found in this meta-analysis, CSF inflammatory cytokines may be used as biomarkers for these diseases in the future.
有人认为细胞因子介导的炎症在包括阿尔茨海默病(AD)、帕金森病(PD)和肌萎缩侧索硬化症(ALS)在内的神经退行性疾病的发病和/或发展中起着关键作用。然而,临床研究对 AD、PD 和 ALS 患者循环中异常细胞因子水平的结果不一致。以前的研究使用荟萃分析来解决 AD、PD 和 ALS 患者血液细胞因子水平的不一致数据。在这里,我们对 AD、PD 和 ALS 患者脑脊液中炎症细胞因子的数据进行了系统评价,并试图通过荟萃分析技术定量总结脑脊液炎症细胞因子数据。从 Pubmed 和 Web of Science 进行的系统搜索确定了 71 篇文章,其中包括 2629 名 AD 患者和 2049 名对照者进行荟萃分析。随机效应荟萃分析表明,与对照组相比,AD 患者脑脊液中的 TGF-β、MCP-1 和 YKL-40 水平显著升高。此外,PD 患者脑脊液中 TGF-β1、IL-6 和 IL-1β 水平升高。此外,与对照组相比,ALS 患者的 G-CSF、IL-2、IL-15、IL-17、MCP-1、MIP-1α、TNF-α 和 VEGF 水平显著升高。总之,这些结果不仅加强了神经退行性疾病伴有炎症反应增强的临床证据,而且还揭示了 AD、PD 和 ALS 患者中枢神经系统中独特的炎症反应特征。鉴于本荟萃分析中发现一些细胞因子与神经退行性疾病之间存在很强的关联,脑脊液炎症细胞因子将来可能被用作这些疾病的生物标志物。