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A machine learning model and identification of immune infiltration for chronic obstructive pulmonary disease based on disulfidptosis-related genes
by
Li, Sijun
, Meng, Xiayan
, Yang, Shixiong
, Huang, Aichun
, Lin, Yanrong
, Lan, Yanqun
, He, Huawei
, Li, Weiwen
, Zhu, Qingdong
, Wei, Xiaoying
in
Analysis
/ Biomedical and Life Sciences
/ Biomedicine
/ Care and treatment
/ Cell death
/ Cell differentiation
/ Chronic obstructive pulmonary disease
/ Correlation analysis
/ Datasets
/ Diagnosis
/ Disulfidptosis
/ Disulfidptosis-related genes
/ Gene Expression
/ Gene Expression Profiling
/ Gene Regulatory Networks
/ Generalized linear models
/ Human Genetics
/ Humans
/ Immune cells
/ Infiltration
/ Learning algorithms
/ Lung diseases
/ Lung diseases, Obstructive
/ Machine Learning
/ Machine learning model
/ Microarrays
/ Nomograms
/ Pathogenesis
/ Patients
/ Precision medicine
/ Pulmonary Disease, Chronic Obstructive - genetics
/ Pulmonary Disease, Chronic Obstructive - immunology
/ Pulmonary function tests
/ Support vector machines
2025
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A machine learning model and identification of immune infiltration for chronic obstructive pulmonary disease based on disulfidptosis-related genes
by
Li, Sijun
, Meng, Xiayan
, Yang, Shixiong
, Huang, Aichun
, Lin, Yanrong
, Lan, Yanqun
, He, Huawei
, Li, Weiwen
, Zhu, Qingdong
, Wei, Xiaoying
in
Analysis
/ Biomedical and Life Sciences
/ Biomedicine
/ Care and treatment
/ Cell death
/ Cell differentiation
/ Chronic obstructive pulmonary disease
/ Correlation analysis
/ Datasets
/ Diagnosis
/ Disulfidptosis
/ Disulfidptosis-related genes
/ Gene Expression
/ Gene Expression Profiling
/ Gene Regulatory Networks
/ Generalized linear models
/ Human Genetics
/ Humans
/ Immune cells
/ Infiltration
/ Learning algorithms
/ Lung diseases
/ Lung diseases, Obstructive
/ Machine Learning
/ Machine learning model
/ Microarrays
/ Nomograms
/ Pathogenesis
/ Patients
/ Precision medicine
/ Pulmonary Disease, Chronic Obstructive - genetics
/ Pulmonary Disease, Chronic Obstructive - immunology
/ Pulmonary function tests
/ Support vector machines
2025
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A machine learning model and identification of immune infiltration for chronic obstructive pulmonary disease based on disulfidptosis-related genes
by
Li, Sijun
, Meng, Xiayan
, Yang, Shixiong
, Huang, Aichun
, Lin, Yanrong
, Lan, Yanqun
, He, Huawei
, Li, Weiwen
, Zhu, Qingdong
, Wei, Xiaoying
in
Analysis
/ Biomedical and Life Sciences
/ Biomedicine
/ Care and treatment
/ Cell death
/ Cell differentiation
/ Chronic obstructive pulmonary disease
/ Correlation analysis
/ Datasets
/ Diagnosis
/ Disulfidptosis
/ Disulfidptosis-related genes
/ Gene Expression
/ Gene Expression Profiling
/ Gene Regulatory Networks
/ Generalized linear models
/ Human Genetics
/ Humans
/ Immune cells
/ Infiltration
/ Learning algorithms
/ Lung diseases
/ Lung diseases, Obstructive
/ Machine Learning
/ Machine learning model
/ Microarrays
/ Nomograms
/ Pathogenesis
/ Patients
/ Precision medicine
/ Pulmonary Disease, Chronic Obstructive - genetics
/ Pulmonary Disease, Chronic Obstructive - immunology
/ Pulmonary function tests
/ Support vector machines
2025
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A machine learning model and identification of immune infiltration for chronic obstructive pulmonary disease based on disulfidptosis-related genes
Journal Article
A machine learning model and identification of immune infiltration for chronic obstructive pulmonary disease based on disulfidptosis-related genes
2025
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Overview
Background
Chronic obstructive pulmonary disease (COPD) is a chronic and progressive lung disease. Disulfidptosis-related genes (DRGs) may be involved in the pathogenesis of COPD. From the perspective of predictive, preventive, and personalized medicine (PPPM), clarifying the role of disulfidptosis in the development of COPD could provide a opportunity for primary prediction, targeted prevention, and personalized treatment of the disease.
Methods
We analyzed the expression profiles of DRGs and immune cell infiltration in COPD patients by using the GSE38974 dataset. According to the DRGs, molecular clusters and related immune cell infiltration levels were explored in individuals with COPD. Next, co-expression modules and cluster-specific differentially expressed genes were identified by the Weighted Gene Co-expression Network Analysis (WGCNA). Comparing the performance of the random forest (RF), support vector machine (SVM), generalized linear model (GLM), and eXtreme Gradient Boosting (XGB), we constructed the ptimal machine learning model.
Results
DE-DRGs, differential immune cells and two clusters were identified. Notable difference in DRGs, immune cell populations, biological processes, and pathway behaviors were noted among the two clusters. Besides, significant differences in DRGs, immune cells, biological functions, and pathway activities were observed between the two clusters.A nomogram was created to aid in the practical application of clinical procedures. The SVM model achieved the best results in differentiating COPD patients across various clusters. Following that, we identified the top five genes as predictor genes via SVM model. These five genes related to the model were strongly linked to traits of the individuals with COPD.
Conclusion
Our study demonstrated the relationship between disulfidptosis and COPD and established an optimal machine-learning model to evaluate the subtypes and traits of COPD. DRGs serve as a target for future predictive diagnostics, targeted prevention, and individualized therapy in COPD, facilitating the transition from reactive medical services to PPPM in the management of the disease.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
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