Zhang Yuchen, Tian Jinzhou, Ni Jingnian, Wei Mingqing, Li Ting, Shi Jing
Department of Neurology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100700, China.
Brain Sci. 2023 Sep 23;13(10):1364. doi: 10.3390/brainsci13101364.
The pathogenesis associated with Alzheimer's disease (AD) is particularly complicated, and early diagnosis and course monitoring of the disease are not ideal based on the available core biomarkers. As a biomarker closely related to neuroinflammation, YKL-40 provides a potential scalable approach in AD, but its association remains controversial and inconclusive with AD. We conducted this study to assess the utility of YKL-40 levels in peripheral blood and cerebrospinal fluid (CSF) of AD patients and healthy controls (HCs) by meta-analysis. We systematically searched and screened relevant trials for comparing YKL-40 levels between AD patients and HCs in PubMed, Embase, Cochrane, and Web of Science, with a search deadline of 14 March 2023 for each database. A total of 17 eligible and relevant studies involving 1811 subjects, including 949 AD patients and 862 HCs, were included. The results showed that YKL-40 levels in the peripheral blood of AD patients and HCs did not possess significant differences. Subgroup analysis showed YKL-40 significantly differed in plasma (SMD = 0.527, 95%CI: [0.302, 0.752]; = 0.000), but did not in serum. In the case of comparison with HCs, YKL-40 was significantly higher in CSF of AD patients (SMD = 0.893, 95%CI: [0.665, 1.121]; = 0.000). Besides that, when we performed a combined analysis of total YKL-40 in both peripheral blood and CSF, overall YKL-40 concentrations were also significantly increased among AD patients (SMD = 0.608, 95%CI: [0.272, 0.943]; = 0.000). YKL-40 provides support and rationale for the neuroinflammatory pathogenesis of AD. The significance of CSF levels of YKL-40 for early screening of AD is definite. Plasma levels of YKL-40 also appear to assist in discriminating AD patients from HCs, which facilitates early screening and monitoring of the natural course of AD.
阿尔茨海默病(AD)的发病机制特别复杂,基于现有的核心生物标志物,该疾病的早期诊断和病程监测并不理想。作为一种与神经炎症密切相关的生物标志物,YKL-40为AD提供了一种潜在的可扩展研究方法,但其与AD的关联仍存在争议且尚无定论。我们进行了这项荟萃分析研究,以评估YKL-40水平在AD患者和健康对照(HCs)外周血和脑脊液(CSF)中的效用。我们系统地检索和筛选了在PubMed、Embase、Cochrane和Web of Science中比较AD患者和HCs之间YKL-40水平的相关试验,每个数据库的检索截止日期为2023年3月14日。总共纳入了17项符合条件的相关研究,涉及1811名受试者,其中包括949名AD患者和862名HCs。结果显示,AD患者和HCs外周血中的YKL-40水平没有显著差异。亚组分析显示,YKL-40在血浆中有显著差异(标准化均数差[SMD]=0.527,95%置信区间[CI]:[0.302,0.752];P=0.000),但在血清中没有。与HCs相比,AD患者脑脊液中的YKL-40显著更高(SMD=0.893,95%CI:[0.665,1.121];P=0.000)。除此之外,当我们对外周血和脑脊液中的总YKL-40进行联合分析时,AD患者中YKL-40的总体浓度也显著升高(SMD=0.608,95%CI:[0.272,0.943];P=0.000)。YKL-40为AD的神经炎症发病机制提供了支持和理论依据。YKL-40脑脊液水平对AD早期筛查的意义是明确的。YKL-40血浆水平似乎也有助于区分AD患者和HCs,这有助于AD自然病程的早期筛查和监测。