基于遗传算法的堆栈集成学习模型用于早期阿尔茨海默病的检测

T. T. Khoei, M. Labuhn, Toro Dama Caleb, Wen-Chen Hu, N. Kaabouch
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引用次数: 7

摘要

阿尔茨海默病(AD)影响着全世界5000万人,是美国第六大死因。然而,阿尔茨海默病患者没有治愈或治疗方法;因此,早期发现本病对提高患者的生活质量具有重要意义。已经提出了几项研究来检测和区分不同的阿尔茨海默病群体,尽管这些研究大多只关注于区分健康人群和阿尔茨海默病患者。这些研究也没有确定最可靠的生物标志物来提供更准确的结果,也没有使用最佳超参数来提供最佳结果。为了解决这些问题,我们开发了一个模型,可以更好地区分健康人(认知正常)、轻度认知障碍患者和阿尔茨海默病患者。为此,我们将基于堆栈的集成学习(由四个传统分类器组成)与超参数调谐技术(遗传算法)相结合。对模型的准确性、精密度、召回率和f1评分进行评价。仿真结果表明,使用遗传算法的基于叠加的集成学习在区分CN、MCI和AD组方面提供了96.7%的准确率、96.5%的召回率、97.9%的精度和97.1%的f1分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Stacking-based Ensemble Learning Model with Genetic Algorithm For detecting Early Stages of Alzheimer’s Disease
Alzheimer's disease (AD) affects fifty million people worldwide and is the sixth cause of death in the United States. However, there is no cure or treatment for patients with AD; thus, it is important to detect this disease at an early stage to improve patients' lives qualities. Several studies have been proposed to detect and differentiate between different AD groups, although most of these works only focused on differentiating between healthy people and people with Alzheimer's. These studies also did not identify the most reliable biomarkers to provide more accurate results and did not use the best hyperparameters to provide optimal results. To address these issues, we developed a model that leads to a better performance in differentiating between healthy people (cognitively normal), people with mild cognitive impairment, and people with Alzheimer’s disease. For this purpose, we combined a stacking-based ensemble learning, consisting of four traditional classifiers, with a hyperparameter tuning technique, a genetic algorithm. The model was evaluated in terms of accuracy, precision, recall, and F1-score. The simulation results show that stacking-based ensemble learning, using genetic algorithm, provides 96.7% accuracy, 96.5% recall, 97.9% precision, and 97.1% F1-score in differentiating between CN, MCI, and AD groups.
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