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基于当前脑脊液标志物和生物流体中铁含量的阿尔茨海默病患者的机器学习分析

Machine Learning Profiling of Alzheimer's Disease Patients Based on Current Cerebrospinal Fluid Markers and Iron Content in Biofluids.

作者信息

Ficiarà Eleonora, Boschi Silvia, Ansari Shoeb, D'Agata Federico, Abollino Ornella, Caroppo Paola, Di Fede Giuseppe, Indaco Antonio, Rainero Innocenzo, Guiot Caterina

机构信息

Department of Neurosciences "Rita Levi Montalcini", University of Torino, Torino, Italy.

Department NEUROFARBA, University of Firenze, Firenze, Italy.

出版信息

Front Aging Neurosci. 2021 Feb 22;13:607858. doi: 10.3389/fnagi.2021.607858. eCollection 2021.

DOI:10.3389/fnagi.2021.607858
PMID:33692679
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7937894/
Abstract

Alzheimer's disease (AD) is the most common form of dementia, characterized by a complex etiology that makes therapeutic strategies still not effective. A true understanding of key pathological mechanisms and new biomarkers are needed, to identify alternative disease-modifying therapies counteracting the disease progression. Iron is an essential element for brain metabolism and its imbalance is implicated in neurodegeneration, due to its potential neurotoxic effect. However, the role of iron in different stages of dementia is not clearly established. This study aimed to investigate the potential impact of iron both in cerebrospinal fluid (CSF) and in serum to improve early diagnosis and the related therapeutic possibility. In addition to standard clinical method to detect iron in serum, a precise quantification of total iron in CSF was performed using graphite-furnace atomic absorption spectrometry in patients affected by AD, mild cognitive impairment, frontotemporal dementia, and non-demented neurological controls. The application of machine learning techniques, such as clustering analysis and multiclassification algorithms, showed a new potential stratification of patients exploiting iron-related data. The results support the involvement of iron dysregulation and its potential interaction with biomarkers (Tau protein and Amyloid-beta) in the pathophysiology and progression of dementia.

摘要

阿尔茨海默病(AD)是最常见的痴呆形式,其病因复杂,导致治疗策略仍然无效。需要真正了解关键的病理机制和新的生物标志物,以确定能够对抗疾病进展的替代性疾病修饰疗法。铁是大脑新陈代谢所必需的元素,由于其潜在的神经毒性作用,铁失衡与神经退行性变有关。然而,铁在痴呆不同阶段的作用尚未明确确立。本研究旨在调查脑脊液(CSF)和血清中铁的潜在影响,以改善早期诊断及相关治疗可能性。除了检测血清中铁的标准临床方法外,还使用石墨炉原子吸收光谱法对AD、轻度认知障碍、额颞叶痴呆患者以及非痴呆神经对照患者的脑脊液中的总铁进行了精确量化。机器学习技术(如聚类分析和多分类算法)的应用显示,利用与铁相关的数据对患者进行新的潜在分层。这些结果支持铁调节异常及其与生物标志物(Tau蛋白和淀粉样β蛋白)在痴呆病理生理学和进展中的潜在相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7f7/7937894/0a655c4ceeb7/fnagi-13-607858-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7f7/7937894/a48e312023c0/fnagi-13-607858-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7f7/7937894/4d30aa490b6c/fnagi-13-607858-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7f7/7937894/4bc798f91da5/fnagi-13-607858-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7f7/7937894/28411a550f98/fnagi-13-607858-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7f7/7937894/0a655c4ceeb7/fnagi-13-607858-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7f7/7937894/a48e312023c0/fnagi-13-607858-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7f7/7937894/4d30aa490b6c/fnagi-13-607858-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7f7/7937894/4bc798f91da5/fnagi-13-607858-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7f7/7937894/28411a550f98/fnagi-13-607858-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7f7/7937894/0a655c4ceeb7/fnagi-13-607858-g0005.jpg

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