产前和青少年酒精暴露,神经炎症和阿尔茨海默病:网络meta分析方法

Lazer Gerlikhman, Ujjal Das, Dipak K. Sarkar
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摘要

摘要目的本综述旨在确定发育性酒精暴露与其对老年痴呆症(AD)的潜在影响之间的联系。我们采用网络荟萃分析方法,从文献和基因表达综合(GEO)数据集检查基因折叠变化。我们的目的是研究产前酒精暴露(PAE)和/或青少年酒精暴露(AAE)是否会激活特定的神经炎症基因,从而潜在地增加AD发展的风险。我们使用网络元分析方法对大脑数据集进行了全面分析。通过综合文献和GEO数据集的基因折叠变化,我们研究了发育性酒精暴露对未来患AD风险增加的潜在影响。我们的研究结果揭示了酒精暴露与大脑关键功能类别和疾病之间的显著关联。酒精暴露与“炎症反应”和“神经系统发育和功能”类别密切相关,表明大脑中的炎症反应和对神经系统完整性的有害影响。此外,我们还观察到与“机体损伤与异常”和“细胞死亡与存活”的联系。通路分析显示神经炎症、ERK/MAPK信号通路、淀粉样蛋白加工、IL-1信号通路和钙信号通路失调,提示它们可能参与酒精诱导的神经毒性。本综述强调了认识到发育性酒精暴露是AD的潜在危险因素的必要性,并阐明了可能导致酒精诱导神经毒性的潜在机制。通过扩大我们对这些机制的理解,我们可以更好地解决发育性酒精暴露与神经退行性疾病(如AD)之间的复杂关系。
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Prenatal and adolescent alcohol exposure, neuroinflammation, and Alzheimer’s disease: a network meta analysis approach
Abstract Objectives This review aims to determine the connection between developmental alcohol exposure and its potential impact on Alzheimer's disease (AD) later in life. We employ a network meta-analysis approach and examine gene fold changes from literature and Gene Expression Omnibus (GEO) datasets. Our goal is to investigate whether prenatal alcohol exposure (PAE) and/or adolescent alcohol exposure (AAE) could activate specific neuroinflammatory genes, potentially increasing the risk of AD development. Content We conducted a comprehensive analysis of brain datasets using a network meta-analysis approach. By synthesizing gene fold changes from literature and GEO datasets, we examined the potential impact of developmental alcohol exposure on increased risk of developing AD in the future. Summary Our findings reveal significant associations between alcohol exposure and critical functional categories and diseases in the brain. Alcohol exposure was strongly linked to the “Inflammatory Response” and “Nervous System Development and Function” categories, indicative of inflammatory reactions in the brain and detrimental effects on nervous system integrity. Furthermore, we observed links with “Organismal Injury and Abnormalities” and “Cell Death and Survival.” Pathway analysis revealed dysregulation in neuroinflammatory, ERK/MAPK signaling, amyloid processing, IL-1 signaling and calcium signaling pathways, suggesting their potential involvement in alcohol-induced neurotoxicity. Outlook This review highlights the necessity of recognizing developmental alcohol exposure as a potential risk factor for AD and shed light on the underlying mechanisms that may contribute to alcohol-induced neurotoxicity. By expanding our understanding of these mechanisms, we can better address the complex relationship between developmental alcohol exposure and neurodegenerative disorders like AD.
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