Identification of osteoporosis based on gene biomarkers using support vector machine.

IF 1.6
Open medicine (Warsaw, Poland) Pub Date : 2022-07-07 eCollection Date: 2022-01-01 DOI:10.1515/med-2022-0507
Nanning Lv, Zhangzhe Zhou, Shuangjun He, Xiaofeng Shao, Xinfeng Zhou, Xiaoxiao Feng, Zhonglai Qian, Yijian Zhang, Mingming Liu
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引用次数: 1

Abstract

Osteoporosis is a major health concern worldwide. The present study aimed to identify effective biomarkers for osteoporosis detection. In osteoporosis, 559 differentially expressed genes (DEGs) were enriched in PI3K-Akt signaling pathway and Foxo signaling pathway. Weighted gene co-expression network analysis showed that green, pink, and tan modules were clinically significant modules, and that six genes (VEGFA, DDX5, SOD2, HNRNPD, EIF5B, and HSP90B1) were identified as "real" hub genes in the protein-protein interaction network, co-expression network, and 559 DEGs. The sensitivity and specificity of the support vector machine (SVM) for identifying patients with osteoporosis was 100%, with an area under curve of 1 in both training and validation datasets. Our results indicated that the current system using the SVM method could identify patients with osteoporosis.

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Abstract Image

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基于支持向量机的基因生物标记识别骨质疏松症。
骨质疏松症是世界范围内的一个主要健康问题。本研究旨在确定骨质疏松症检测的有效生物标志物。在骨质疏松症中,PI3K-Akt信号通路和Foxo信号通路中有559个差异表达基因(DEGs)富集。加权基因共表达网络分析显示,绿色、粉色和棕褐色模块是具有临床意义的模块,6个基因(VEGFA、DDX5、SOD2、HNRNPD、EIF5B和HSP90B1)在蛋白-蛋白相互作用网络、共表达网络和559 DEGs中被鉴定为“真正的”枢纽基因。支持向量机(SVM)识别骨质疏松患者的敏感性和特异性均为100%,训练集和验证集的曲线下面积均为1。我们的结果表明,目前使用SVM方法的系统可以识别骨质疏松症患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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