Identification of fatty acid metabolism signature genes in patients with pulmonary arterial hypertension using WGCNA and machine learning

被引:0
作者
Liu, Xibang [1 ]
Wu, Dandan [1 ]
Bao, Chunmiao [1 ]
Huang, Zeen [1 ]
Wang, Weiwei [1 ]
Sun, Lili [1 ]
Qiu, Lin [1 ]
机构
[1] Yuyao Peoples Hosp Zhejiang Prov, Affiliated Yangming Hosp, Dept Resp & Crit Care Med, Chengdong Rd 800, Yuyao 315400, Zhejiang, Peoples R China
关键词
Fatty acid metabolism; pulmonary arterial hypertension; machine learning; weighted gene co-expression network analysis; immune cell infiltration; differentially expressed gene; PATHOGENESIS; EXPRESSION; GUIDELINES; ARV1; SCO1;
D O I
10.1177/03000605241277740
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective To investigate the signature genes of fatty acid metabolism and their association with immune cells in pulmonary arterial hypertension (PAH).Methods Fatty acid metabolism-related genes were obtained from the GeneCards database. In this retrospective study, a PAH-related dataset was downloaded from the Gene Expression Omnibus database and analyzed to identify differentially expressed genes (DEGs). Weighted gene co-expression network analysis (WGCNA) and machine learning algorithms, including least absolute shrinkage and selection operator (LASSO) and random forest, were used to identify the signature genes. Diagnostic efficiency was assessed by receiver operating characteristic (ROC) curve analysis and a nomogram. Immune cell infiltration was subsequently classified using CIBERSORT.Results In total, 817 DEGs were screened from the GSE33463 dataset. The data were clustered into six modules via WGCNA, and the MEdarkred module was significantly related to PAH. The LASSO and random forest algorithms identified five signature genes: ARV1, KCNJ2, PEX11B, PITPNC1, and SCO1. The areas under the ROC curves of these signature genes were 0.917, 0.934, 0.947, 0.963, and 0.940, respectively. CIBERSORT suggested these signature genes may participate in immune cell infiltration.Conclusions ARV1, KCNJ2, PEX11B, PITPNC1, and SCO1 show remarkable diagnostic performance in PAH and are involved in immune cell infiltration.
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页数:14
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