Exploring the Efficiency of Hub Genes in Identification of Alzheimer Disease

Maysa O. Mohamed, N. Salem, V. F. Ghoneim
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Abstract

Alzheimer’s disease (AD) is a kind of dementia that gets worse over time, it results in a loss in memory and cognitive function. Consequently, it is very important to diagnose AD in its early stages. This diagnosis is required using different methods through certain alternative approaches. Different techniques such as imaging, clinical, genetic, and fluid biomarker-based pattern classification methods are used for developing predictive models of AD dementia. In this paper, two approaches are used to recognize the prognostic and diagnostic biomarkers that can discriminate between AD and non-AD patients. The publicly available microarray of gene expression datasets from six brain regions are used. The first approach is used to explore the biomarker gene in each region of the six brain regions and in turns investigate the best region that used for AD identification. The second approach is to create the gene network based on extracting the most significant gene in each region separately and extract the hub one of each network. Then, hub genes in each region are used in a classification step to investigate the efficiency of such genes in recognizing AD patients.The highest 50 genes from each region were used in both approaches. In the classification step, the feature selection based on T-test followed by the Support Vector Machine (SVM) classifier is used. Experimental results show reliability of SVM with this kind of gene expression data. The first approach yields best classification results with Entorhinal Cortex (EC) region reaching 95.7%. The second approach proves that hub genes are more efficient in identification of AD improving the classification accuracy with all brain regions reaching 100% accuracy for EC region.
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枢纽基因在阿尔茨海默病鉴定中的作用探讨
阿尔茨海默病(AD)是一种随着时间的推移而恶化的痴呆症,它会导致记忆和认知功能的丧失。因此,在早期诊断AD是非常重要的。这种诊断需要通过某些替代方法使用不同的方法。不同的技术,如成像、临床、遗传和基于流体生物标志物的模式分类方法被用于开发阿尔茨海默氏症的预测模型。本文采用两种方法来识别可区分AD和非AD患者的预后和诊断生物标志物。使用了来自六个大脑区域的基因表达数据集的公开微阵列。第一种方法用于探索六个大脑区域中每个区域的生物标记基因,并依次研究用于阿尔茨海默病鉴定的最佳区域。第二种方法是在分别提取每个区域最显著基因的基础上构建基因网络,并提取每个网络的枢纽基因。然后,在分类步骤中使用每个区域的枢纽基因来研究这些基因识别AD患者的效率。在两种方法中都使用了每个区域中最高的50个基因。在分类步骤中,使用基于t检验的特征选择,然后使用支持向量机(SVM)分类器。实验结果表明支持向量机对这类基因表达数据的处理是可靠的。第一种方法分类效果最好,内嗅皮层(EC)区分类率为95.7%。第二种方法证明hub基因对AD的识别效率更高,对EC区的分类准确率达到100%。
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