Department of Geriatrics, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, China.
Front Endocrinol (Lausanne). 2024 Oct 23;15:1448119. doi: 10.3389/fendo.2024.1448119. eCollection 2024.
Alzheimer's disease (AD) represents a progressive neurodegenerative disorder characterized by the accumulation of misfolded amyloid beta protein, leading to the formation of amyloid plaques and the aggregation of tau protein into neurofibrillary tangles within the cerebral cortex. The role of carbohydrates, particularly apolipoprotein E (ApoE), is pivotal in AD pathogenesis due to its involvement in lipid and cholesterol metabolism, and its status as a genetic predisposition factor for the disease. Despite its significance, the mechanistic contributions of Lipid Metabolism-related Genes (LMGs) to AD remain inadequately elucidated. This research endeavor seeks to bridge this gap by pinpointing biomarkers indicative of early-stage AD, with an emphasis on those linked to immune cell infiltration. To this end, advanced machine-learning algorithms and data derived from the Gene Expression Omnibus (GEO) database have been employed to facilitate the identification of these biomarkers.
Differentially expressed genes (DEGs) were identified by comparing gene expression profiles between healthy individuals and Alzheimer's disease (AD) patients, using data from two Gene Expression Omnibus (GEO) datasets: GSE5281 and GSE138260. Functional enrichment analysis was conducted to elucidate the biological relevance of the DEGs. To ensure the reliability of the results, samples were randomly divided into training and validation sets. The analysis focused on lipid metabolism-related DEGs (LMDEGs) to explore potential biomarkers for AD. Machine learning algorithms, including Support Vector Machine-Recursive Feature Elimination (SVM-RFE) and the Least Absolute Shrinkage and Selection Operator (LASSO) regression model, were applied to identify a key gene biomarker. Additionally, immune cell infiltration and its relationship with the gene biomarker were assessed using the CIBERSORT algorithm. The Integrated Traditional Chinese Medicine (ITCM) database was also referenced to identify Chinese medicines related to lipid metabolism and their possible connection to AD. This comprehensive strategy aims to integrate modern computational methods with traditional medicine to deepen our understanding of AD and its underlying mechanisms.
The study identified 137 genes from a pool of 751 lipid metabolism-related genes (LMGs) significantly associated with autophagy and immune response mechanisms. Through the application of LASSO and SVM-RFE machine-learning techniques, four genes-choline acetyl transferase (CHAT), member RAS oncogene family (RAB4A), acyl-CoA binding domain-containing protein 6 (ACBD6), and alpha-galactosidase A (GLA)-emerged as potential biomarkers for Alzheimer's disease (AD). These genes demonstrated strong therapeutic potential due to their involvement in critical biological pathways. Notably, nine Chinese medicine compounds were identified to target these marker genes, offering a novel treatment approach for AD. Further, ceRNA network analysis revealed complex regulatory interactions involving these genes, underscoring their importance in AD pathology. CIBERSORT analysis highlighted a potential link between changes in the immune microenvironment and CHAT expression levels in AD patients, providing new insights into the immunological dimensions of the disease.
The discovery of these gene markers offers substantial promise for the diagnosis and understanding of Alzheimer's disease (AD). However, further investigation is necessary to validate their clinical utility. This study illuminates the role of Lipid Metabolism-related Genes (LMGs) in AD pathogenesis, offering potential targets for therapeutic intervention. It enhances our grasp of AD's complex mechanisms and paves the way for future research aimed at refining diagnostic and treatment strategies.
阿尔茨海默病(AD)是一种进行性神经退行性疾病,其特征是错误折叠的淀粉样β蛋白的积累,导致淀粉样斑块的形成和微管相关蛋白 tau 的聚集形成神经原纤维缠结在大脑皮层内。碳水化合物的作用,特别是载脂蛋白 E(ApoE),在 AD 的发病机制中至关重要,因为它参与脂质和胆固醇代谢,并且是该疾病的遗传易感性因素。尽管其意义重大,但脂质代谢相关基因(LMGs)对 AD 的机械贡献仍未得到充分阐明。这项研究旨在通过确定指示早期 AD 的生物标志物来弥补这一空白,重点是那些与免疫细胞浸润相关的生物标志物。为此,采用了先进的机器学习算法和来自基因表达综合数据库(GEO)的数据来识别这些生物标志物。
通过比较健康个体和阿尔茨海默病(AD)患者之间的基因表达谱,使用来自两个基因表达综合数据库(GEO)数据集的 GSE5281 和 GSE138260 的数据,确定差异表达基因(DEGs)。进行功能富集分析以阐明 DEGs 的生物学相关性。为了确保结果的可靠性,将样本随机分为训练集和验证集。分析重点是脂质代谢相关的 DEGs(LMDEGs),以探索 AD 的潜在生物标志物。应用支持向量机-递归特征消除(SVM-RFE)和最小绝对收缩和选择算子(LASSO)回归模型等机器学习算法,确定关键基因生物标志物。此外,使用 CIBERSORT 算法评估免疫细胞浸润及其与基因生物标志物的关系。还参考了中药综合数据库(ITCM),以鉴定与脂质代谢相关的中药及其与 AD 的可能联系。该综合策略旨在将现代计算方法与传统医学相结合,以加深我们对 AD 及其潜在机制的理解。
本研究从 751 个脂质代谢相关基因(LMGs)中筛选出 137 个与自噬和免疫反应机制显著相关的基因。通过应用 LASSO 和 SVM-RFE 机器学习技术,胆碱乙酰转移酶(CHAT)、RAS 癌基因家族成员(RAB4A)、酰基辅酶 A 结合域蛋白 6(ACBD6)和α-半乳糖苷酶 A(GLA)这四个基因被确定为潜在的阿尔茨海默病(AD)生物标志物。这些基因由于参与关键的生物学途径而具有很强的治疗潜力。值得注意的是,鉴定出了 9 种针对这些标记基因的中药化合物,为 AD 提供了一种新的治疗方法。此外,ceRNA 网络分析揭示了这些基因涉及的复杂调控相互作用,强调了它们在 AD 病理中的重要性。CIBERSORT 分析突出了 AD 患者中免疫微环境变化与 CHAT 表达水平之间的潜在联系,为该疾病的免疫学方面提供了新的见解。
这些基因标记的发现为阿尔茨海默病(AD)的诊断和理解提供了很大的希望。然而,需要进一步的研究来验证其临床实用性。本研究阐明了脂质代谢相关基因(LMGs)在 AD 发病机制中的作用,为治疗干预提供了潜在的靶点。它增强了我们对 AD 复杂机制的理解,并为未来旨在完善诊断和治疗策略的研究铺平了道路。