Peripheral Blood Monocytes as Biomarkers of Neurodevelopmental Disorders: A Systematic Review and Meta-Analysis.

IF 2.9 2区 心理学 Q1 PSYCHOLOGY, CLINICAL
Xing-Da Ju, Pai-Hao Zhang, Qiang Li, Qiu-Yu Bai, Bo Hu, Jing Xu, Chang Lu
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Abstract

Accumulating evidence implicates immune dysregulation and chronic inflammation in neurodevelopmental disorders (NDDs), often manifesting as abnormal alterations in peripheral blood immune cell levels. The mononuclear phagocyte system, including monocytes and microglia, has been increasingly recognized for its involvement in the pathogenesis of NDDs. However, due to inconsistent findings in the literature, whether monocytes can serve as a reliable biomarker for NDDs remains controversial. To address this issue, we conducted a systematic review and meta-analysis of studies examining monocyte counts in NDD individuals. A comprehensive search was conducted across PubMed, Web of Science, and Scopus databases. Variables extracted for analysis encompassed the author's name, year of study, sample size, patient's age, type of disease, mean, standard deviation of monocytes and sex ratio. A total of 2503 articles were found by searching the three databases. After removed duplicates and screening titles, abstracts, and full texts, 17 articles met the inclusion criteria, and 20 independent studies were included in the meta-analysis. The results indicated significantly increased monocyte counts in 5 type NDDs compared to Typical Development (TD) groups (g = 0.36, 95%CI [0.23, 0.49]). Subgroup analyses revealed no significant differences in monocyte counts across different NDD types, gender, or age. These findings suggest that aberrant alterations in monocyte counts are common in NDD cases, indicating their potential as biomarkers for these conditions. Future research should further investigate the role of monocyte in understanding the mechanisms, early detection, and clinical diagnosis of NDDs.

外周血单核细胞作为神经发育障碍的生物标志物:系统综述和荟萃分析。
越来越多的证据表明,神经发育障碍(ndd)中存在免疫失调和慢性炎症,通常表现为外周血免疫细胞水平的异常改变。单核吞噬细胞系统,包括单核细胞和小胶质细胞,已越来越多地认识到其参与ndd的发病机制。然而,由于文献中不一致的发现,单核细胞是否可以作为ndd的可靠生物标志物仍然存在争议。为了解决这个问题,我们对NDD患者单核细胞计数的研究进行了系统回顾和荟萃分析。在PubMed、Web of Science和Scopus数据库中进行了全面的搜索。提取用于分析的变量包括作者姓名、研究年份、样本量、患者年龄、疾病类型、单核细胞平均值、标准差和性别比例。三个数据库共检索到2503篇文章。在去除重复并筛选标题、摘要和全文后,17篇文章符合纳入标准,20项独立研究被纳入meta分析。结果显示,与典型发育(TD)组相比,5型ndd的单核细胞计数显著增加(g = 0.36, 95%CI[0.23, 0.49])。亚组分析显示,不同NDD类型、性别或年龄的单核细胞计数无显著差异。这些发现表明,单核细胞计数的异常改变在NDD病例中很常见,表明它们有可能作为这些疾病的生物标志物。未来的研究应进一步探讨单核细胞在了解ndd的发病机制、早期发现和临床诊断中的作用。
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
Research on Child and Adolescent Psychopathology
Research on Child and Adolescent Psychopathology Psychology-Developmental and Educational Psychology
CiteScore
5.00
自引率
4.00%
发文量
107
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