Machine learning–guided Huanglian Jiedu decoction targets STING in periodontitis-induced Alzheimer’s Disease

转录组 医学 疾病 体内 神经炎症 神经科学 计算生物学 小胶质细胞 炎症 功能(生物学) 信号转导 药物重新定位 药理学 炎症反应 生物信息学 牙周炎 免疫学 机制(生物学) 外围设备 体外 S100A9型 免疫系统 人参皂甙 治疗方法 海马结构 特征(语言学)
作者
Jie Li,Mingqi Chen,Pan Ren,Guangming Sun,Furong Zhong,Yue Zhu,Ganggang Li,Yiran Fan,Jinxin Chen,Manru Xu,Mengyuan Qiao,Guohua Zhao,Ying Xu,Wenbin Wu
出处
期刊:npj digital medicine [Nature Portfolio]
卷期号:9 (1) 被引量:1
标识
DOI:10.1038/s41746-026-02468-x
摘要

Alzheimer's disease (AD) is a progressive neurodegenerative disorder increasingly associated with peripheral inflammatory conditions such as chronic periodontitis (CP); however, the molecular mechanisms linking these conditions remain poorly understood. Here, we investigated the therapeutic effects of Huanglian Jieddu Decoction (HLJDD) on CP-induced AD using an integrative machine learning-guided multi-omics approach. Analysis of public single-cell RNA-sequencing data revealed pronounced inflammatory activation in microglia from AD samples. We further established a CP-induced AD rat model and performed hippocampal transcriptomic profiling. Multiple complementary machine learning strategies, including Random Forest-based feature selection, support vector machine-based refinement, network modeling, and interpretable model analysis, were applied to prioritize disease-relevant pathways from high-dimensional transcriptomic data. Across models, components of the cGAS-STING signaling pathway consistently exhibited strong and directional contributions to CP-AD pathology, indicating a central inflammatory axis linking peripheral infection to neurodegeneration. Guided by these data-driven insights, in vivo and in vitro experiments demonstrated that HLJDD suppressed cGAS-STING activation, attenuated neuroinflammation, and improved cognitive function in CP-induced AD models. Collectively, this study highlights the value of machine learning-assisted transcriptomic interpretation for mechanistic prioritization and identifies HLJDD as a multitarget therapeutic strategy for CP-induced AD.
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