Identification of crucial inflammaging related risk factors in multiple sclerosis

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Mengchu Xu, Huize Wang, Siwei Ren, Bing Wang, Wenyan Yang, Ling Lv, Xianzheng Sha, Wenya Li, Yin Wang
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引用次数: 0

Abstract

Multiple sclerosis (MS) is an immune-mediated disease characterized by inflammatory demyelinating lesions in the central nervous system. Studies have shown that the inflammation is vital to both the onset and progression of MS, where aging plays a key role in it. However, the potential mechanisms on how aging-related inflammation (inflammaging) promotes MS have not been fully understood. Therefore, there is an urgent need to integrate the underlying mechanisms between inflammaging and MS, where meaningful prediction models are needed.First, both aging and disease models were developed using machine learning methods, respectively. Then, an integrated inflammaging model was used to identify relative risk factors, by identifying essential “aging-inflammation-disease” triples. Finally, a series of bioinformatics analyses (including network analysis, enrichment analysis, sensitivity analysis, and pan-cancer analysis) were further used to explore the potential mechanisms between inflammaging and MS.A series of risk factors were identified, such as the protein homeostasis, cellular homeostasis, neurodevelopment and energy metabolism. The inflammaging indices were further validated in different cancer types. Therefore, various risk factors were integrated, and even both the theories of inflammaging and immunosenescence were further confirmed.In conclusion, our study systematically investigated the potential relationships between inflammaging and MS through a series of computational approaches, and could present a novel thought for other aging-related diseases.
识别多发性硬化症中与炎症相关的关键风险因素
多发性硬化症(MS)是一种免疫介导的疾病,以中枢神经系统的炎症性脱髓鞘病变为特征。研究表明,炎症对多发性硬化症的发病和进展都至关重要,而衰老在其中扮演着关键角色。然而,与衰老相关的炎症(炎症aging)如何促进多发性硬化症的潜在机制尚未完全明了。因此,迫切需要整合炎症和多发性硬化症之间的潜在机制,并建立有意义的预测模型。首先,利用机器学习方法分别建立了衰老模型和疾病模型,然后,通过识别 "衰老-炎症-疾病 "三要素,利用综合炎症模型确定相对风险因素。最后,一系列生物信息学分析(包括网络分析、富集分析、敏感性分析和泛癌症分析)被进一步用于探索炎症与多发性硬化症之间的潜在机制。在不同癌症类型中进一步验证了炎症指数。总之,我们的研究通过一系列计算方法系统地研究了炎症与多发性硬化症之间的潜在关系,为其他衰老相关疾病的研究提供了新思路。
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来源期刊
CiteScore
5.70
自引率
2.10%
发文量
669
审稿时长
14 weeks
期刊介绍: Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.
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