Bioinformatics analysis of PANoptosis regulators in the diagnosis and subtyping of steroid-induced osteonecrosis of the femoral head

被引:0
作者
Ding, Qiang [1 ]
Xiong, Bo [2 ]
Liu, Jinfu [1 ]
Rong, Xiangbin [3 ]
Tian, Zhao [1 ]
Chen, Limin [1 ]
Tao, Hongcheng [1 ]
Li, Hao [1 ]
Zeng, Ping [4 ]
机构
[1] Guangxi Univ Chinese Med, Clin Med Coll 1, Nanning, Peoples R China
[2] Yulin Orthoped Hosp Integrated Tradit Chinese & We, Yulin, Peoples R China
[3] Guangxi Univ Chinese Med, Ruikang Hosp, Nanning, Peoples R China
[4] Guangxi Tradit Chinese Med Univ, Affiliated Hosp 1, Nanning 530000, Guangxi Zhuang, Peoples R China
基金
中国国家自然科学基金;
关键词
biomarkers; immune infiltration; machine learning models; molecular subtypes; PANoptosis; SONFH; DUAL-ENERGY-CT; VIRTUAL NONCALCIUM TECHNIQUE; BONE-MARROW INVOLVEMENT; MULTIPLE-MYELOMA; LESIONS; SPINE; EXPERIENCE; ACCURACY; DURIE;
D O I
10.1097/MD.0000000000037837
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this study, we aimed to investigate the involvement of PANoptosis, a form of regulated cell death, in the development of steroid-induced osteonecrosis of the femoral head (SONFH). The underlying pathogenesis of PANoptosis in SONFH remains unclear. To address this, we employed bioinformatics approaches to analyze the key genes associated with PANoptosis. Our analysis was based on the GSE123568 dataset, allowing us to investigate both the expression profiles of PANoptosis-related genes (PRGs) and the immune profiles in SONFHallowing us to investigate the expression profiles of PRGs as well as the immune profiles in SONFH. We conducted cluster classification based on PRGs and assessed immune cell infiltration. Additionally, we used the weighted gene co-expression network analysis (WGCNA) algorithm to identify cluster-specific hub genes. Furthermore, we developed an optimal machine learning model to identify the key predictive genes responsible for SONFH progression. We also constructed a nomogram model with high predictive accuracy for assessing risk factors in SONFH patients, and validated the model using external data (area under the curve; AUC = 1.000). Furthermore, we identified potential drug targets for SONFH through the Coremine medical database. Using the optimal machine learning model, we found that 2 PRGs, CASP1 and MLKL, were significantly correlated with the key predictive genes and exhibited higher expression levels in SONFH. Our analysis revealed the existence of 2 distinct PANoptosis molecular subtypes (C1 and C2) within SONFH. Importantly, we observed significant variations in the distribution of immune cells across these subtypes, with C2 displaying higher levels of immune cell infiltration. Gene set variation analysis indicated that C2 was closely associated with multiple immune responses. In conclusion, our study sheds light on the intricate relationship between PANoptosis and SONFH. We successfully developed a risk predictive model for SONFH patients and different SONFH subtypes. These findings enhance our understanding of the pathogenesis of SONFH and offer potential insights into therapeutic strategies.
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页数:17
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