Cerebrospinal fluid biomarkers for the subtle differentiation of neurodegenerative diseases and psychiatric disorders: A systematic review with network meta-analysis

Brain disorders (Amsterdam, Netherlands) Pub Date : 2026-06-01 Epub Date: 2026-05-25 DOI:10.1016/j.dscb.2026.100319
Xuan Yang , Lan Lei , Ya-Ting Wang , Si-Tong Feng , Bin Chen , Yi Zhang
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引用次数: 0

Abstract

Cerebrospinal fluid (CSF) biomarkers are used to identify or detect the condition of multiple neurodegenerative diseases, even psychiatric disorders. However, discordant results between observational studies failed to meet the expectations of identifying neurodegenerative diseases and psychiatric disorders. We conducted this systematic review and network meta-analyses to investigate the CSF biomarkers in neurodegenerative diseases and psychiatric disorders, which contribute to the diagnosis of these diseases. Studies before September 2023 were searched based on databases. We included observational studies that compared the CSF levels of these biomarkers (Aβ1–​42, tau, p-tau181, and α-synuclein) between healthy controls, neurodegenerative diseases, and psychiatric disorders. We conducted traditional pairwise analysis and network meta-analysis to evaluate the evidence concerning these CSF biomarkers between these neurodegenerative diseases and psychiatric disorders. This network meta-analysis included 117 studies with 25,210 patients to investigate the CSF biomarkers in multiple neurodegenerative diseases and psychiatric disorders (primarily depression, bipolar disorder, and schizophrenia). For CSF Aβ1–​42 levels, there were no statistically significant differences between these groups in network analysis. Regarding CSF t-tau and p-tau181 levels, statistical significance was observed in comparing Alzheimer’s disease (AD) and other diseases, e.g., amyotrophic lateral sclerosis (ALS). Regarding CSF α-synuclein levels, statistical significance was observed in several comparisons, e.g., AD vs. ALS. Conclusively, we identified that CSF Aβ1–​42, t-tau, and p-tau181 might be promising markers distinguishing AD from other neurodegenerative diseases and cognitive impairment. It is conflicting that CSF α-synuclein acts as a marker for diagnosing neurodegenerative diseases and predicts the presence of psychiatric disorders.
神经退行性疾病和精神疾病细微分化的脑脊液生物标志物:网络荟萃分析的系统综述
脑脊液(CSF)生物标志物用于识别或检测多种神经退行性疾病,甚至精神疾病的状况。然而,观察性研究之间不一致的结果未能满足识别神经退行性疾病和精神疾病的期望。我们进行了系统综述和网络荟萃分析,以研究脑脊液生物标志物在神经退行性疾病和精神疾病中的作用,这些生物标志物有助于这些疾病的诊断。在数据库中检索了2023年9月之前的研究。我们纳入了比较健康对照、神经退行性疾病和精神疾病患者脑脊液中这些生物标志物(Aβ1 - 42、tau、p-tau181和α-突触核蛋白)水平的观察性研究。我们通过传统的两两分析和网络荟萃分析来评估这些神经退行性疾病和精神疾病之间脑脊液生物标志物的证据。该网络荟萃分析包括117项研究,涉及25,210例患者,以调查多种神经退行性疾病和精神疾病(主要是抑郁症、双相情感障碍和精神分裂症)的脑脊液生物标志物。脑脊液a - β1 - 42水平,两组间网络分析差异无统计学意义。脑脊液t-tau和p-tau181水平在阿尔茨海默病(AD)与其他疾病(如肌萎缩侧索硬化症(ALS))比较中有统计学意义。脑脊液α-突触核蛋白水平在AD与ALS等多个比较中均有统计学意义。最后,我们确定CSF a - β1 - 42、t-tau和p-tau181可能是区分AD与其他神经退行性疾病和认知障碍的有希望的标志物。脑脊液α-突触核蛋白作为诊断神经退行性疾病和预测精神疾病存在的标志物存在矛盾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Brain disorders (Amsterdam, Netherlands)
Brain disorders (Amsterdam, Netherlands) Neurology, Clinical Neurology
CiteScore
1.90
自引率
0.00%
发文量
0
审稿时长
51 days
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