Enhanced detection of mild cognitive impairment in Alzheimer's disease: a hybrid model integrating dual biomarkers and advanced machine learning.

IF 3.8 2区 医学 Q2 GERIATRICS & GERONTOLOGY BMC Geriatrics Pub Date : 2025-01-23 DOI:10.1186/s12877-025-05683-5
John Sahaya Rani Alex, R Roshini, G Maneesha, Jeetashree Aparajeeta, B Priyadarshini, Chih-Yang Lin, Chi-Wen Lung
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Abstract

Alzheimer's disease (AD) is a complex, progressive, and irreversible neurodegenerative disorder marked by cognitive decline and memory loss. Early diagnosis is the most effective strategy to slow the disease's progression. Mild Cognitive Impairment (MCI) is frequently viewed as a crucial stage before the onset of AD, making it the ideal period for therapeutic intervention. AD is marked by the buildup of amyloid-beta (Aβ) plaques and tau neurofibrillary tangles (NFTs), which are believed to cause neuronal loss and cognitive decline. Both Aβ plaques and NFTs accumulate for many years before the clinical symptoms become apparent in AD. As a result, in this study, CerebroSpinal Fluid (CSF) biomarker information is combined with hippocampal volumes to differentiate between MCI and AD. For this, a novel two-stage hybrid learning model that leverages 3D CNN and the notion of a Fuzzy and Machine learning model is proposed. A 3D-CNN architecture is employed to segment the hippocampus from the structural brain 3D-MR images and quantify the hippocampus volume. In stage 1, the hippocampus volume is passed through thirteen machine learning models and fuzzy clustering for classifying symptomatic AD and healthy brain (Normal Control - NC). The CSF data is fuzzified to capture the inherent uncertainty and overlap in clinical data. The identified symptomatic AD data in the stage1 are further classified into MCI and AD with the aid of a fuzzified CSF biomarker in stage 2. The experimental work presented in this study utilized the Alzheimer's Disease Neuroimaging Initiative (ADNI) dataset. The proposed hybrid model achieved an average accuracy of 93.6% for distinguishing between NC and symptomatic AD and 93.7% for discriminating between MCI and AD. This approach enhances diagnostic accuracy and provides a more comprehensive assessment, allowing for earlier and more targeted therapeutic interventions.

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阿尔茨海默病轻度认知障碍的增强检测:结合双生物标志物和先进机器学习的混合模型。
阿尔茨海默病(AD)是一种复杂的、进行性的、不可逆的神经退行性疾病,其特征是认知能力下降和记忆丧失。早期诊断是减缓疾病进展的最有效策略。轻度认知障碍(Mild Cognitive Impairment, MCI)通常被认为是AD发病前的一个关键阶段,是进行治疗干预的理想时期。阿尔茨海默氏症的特征是淀粉样蛋白斑块和tau神经原纤维缠结(nft)的积累,这被认为会导致神经元丢失和认知能力下降。在阿尔茨海默病的临床症状变得明显之前,β斑块和nft都会积累多年。因此,在本研究中,脑脊液(CSF)生物标志物信息与海马体积相结合,以区分MCI和AD。为此,提出了一种新的两阶段混合学习模型,该模型利用3D CNN和模糊和机器学习模型的概念。采用3D-CNN架构从脑结构3D-MR图像中分割海马,量化海马体积。在第1阶段,海马体积通过13个机器学习模型和模糊聚类来分类症状性AD和健康大脑(正常控制- NC)。脑脊液数据被模糊化,以捕捉临床数据中固有的不确定性和重叠。在阶段1中识别出的症状性AD数据在阶段2中借助模糊化的CSF生物标志物进一步分为MCI和AD。本研究中提出的实验工作利用了阿尔茨海默病神经影像学倡议(ADNI)数据集。所提出的混合模型区分NC和症状性AD的平均准确率为93.6%,区分MCI和AD的平均准确率为93.7%。这种方法提高了诊断的准确性,提供了更全面的评估,允许更早和更有针对性的治疗干预。
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来源期刊
BMC Geriatrics
BMC Geriatrics GERIATRICS & GERONTOLOGY-
CiteScore
5.70
自引率
7.30%
发文量
873
审稿时长
20 weeks
期刊介绍: BMC Geriatrics is an open access journal publishing original peer-reviewed research articles in all aspects of the health and healthcare of older people, including the effects of healthcare systems and policies. The journal also welcomes research focused on the aging process, including cellular, genetic, and physiological processes and cognitive modifications.
期刊最新文献
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