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Establishment of a prediction model of changing trends in cardiac hypertrophy disease based on microarray data screening

机译:基于微阵列数据筛选的心脏肥大疾病变化趋势预测模型的建立

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The aim of the present study was to construct a mathematical model to predict the changing trends of cardiac hypertrophy at gene level. Microarray data were downloaded from Gene Expression Omnibus database (accession, GSE21600), which included 35 samples harvested from the heart of Wistar rats on postoperative days 1 (D1 group), 6 (D6 group) and 42 (D42 group) following aorta ligation and sham operated Wistar rats, respectively. Each group contained six samples, with the exception of the samples harvested from the aorta ligated group after 6 days, where n= 5. Differentially expressed genes (DEGs) were identified using a Limma package in R. Hierarchical clustering analysis was performed on common DEGs in order to construct a linear equation between the D1 and D42 groups, using linear discriminant analysis. Subsequent verification was performed using receiver operating characteristic (ROC) curve and the measurement data at day 42. A total of 319, 44 and 57 DEGs were detected in D1, D6 and D42 sample groups, respectively. AKIP1, ANKRD23, LTBP2, TGF-beta 2 and TNFRSF12A were identified as common DEGs in all groups. The predicted linear equation between D1 and D42 group was calculated to be y = 1.526x-186.671. Assessment of the ROC curve demonstrated that the area under the curve was 0.831, with a specificity and sensitivity of 0.8. As compared with the predictive and measurement data at day 42, the consistency of the two sets of data was 76.5%. In conclusion, the present model may contribute to the early prediction of changing trends in cardiac hypertrophy disease at gene level.
机译:本研究的目的是建立一个数学模型来预测基因水平上心脏肥大的变化趋势。从Gene Expression Omnibus数据库(登录号,GSE21600)下载了微阵列数据,其中包括在主动脉结扎后第1天(D1组),第6天(D6组)和第42天(D42组)从Wistar大鼠心脏采集的35个样本。假手术分别为Wistar大鼠。除6天后从主动脉结扎组收集的样本(n = 5)外,每组均包含6个样本。使用R的Limma软件包鉴定了差异表达的基因(DEG)。对常见的DEG进行了层次聚类分析为了使用线性判别分析在D1和D42组之间构建线性方程。随后使用接收器工作特性(ROC)曲线和第42天的测量数据进行验证。在D1,D6和D42样品组中分别检测到319、44和57个DEG。 AKIP1,ANKRD23,LTBP2,TGF-beta 2和TNFRSF12A被确定为所有组中的常见DEG。 D1和D42组之间的预测线性方程计算为y = 1.526x-186.671。 ROC曲线的评估表明,曲线下的面积为0.831,特异性和敏感性为0.8。与第42天的预测和测量数据相比,两组数据的一致性为76.5%。总之,本模型可有助于在基因水平上早期预测心脏肥大疾病变化趋势。

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