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pmid:40656047

Integrating weighted gene co-expression network analysis and machine learning to elucidate neural characteristics in a mouse model of depression.

Jinli Gao · Qinglang Wang · Jie Liu · Siqian Zheng · Jiahong Liu · Zhiyong Gao · Cheng Zhu

Frontiers in psychiatry · 2025 doi:10.3389/fpsyt.2025.1564095

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Experiment

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Data

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Integrating weighted gene co-expression network analysis and machine learning to elucidate neural characteristics in a mouse model of depression.
doi
10.3389/fpsyt.2025.1564095
pmid
40656047
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Jinli Gao
[1]
Qinglang Wang
[2]
Jie Liu
[3]
Siqian Zheng
[4]
Jiahong Liu
[5]
Zhiyong Gao
[6]
Cheng Zhu
journal
Frontiers in psychiatry
year
2025
abstract
Introduction: An AI-assisted deep learning strategy was applied to analyze the neurobiological characteristics of depression in mouse models. Integration of weighted gene co-expression network analysis (WGCNA) with the random forest algorithm enabled the identification of critical genes strongly associated with depression onset, offering theoretical support and potential biomarkers for early diagnosis and precision treatment. Methods: Gene expression data from depression-related mouse models were obtained from public GEO datasets (e.g., GSE102556) and normalized using Z-score transformation. WGCNA was employed to construct gene co-expression networks and explore associations between modules and depression-like behavioral phenotypes. Depression-related gene modules were identified and subjected to feature selection using the random forest model. The biological relevance of selected genes was further assessed, and model accuracy was validated through performance evaluation. Results: Our findings revealed significant differential expression of genes such as Oprm1, BDNF, Tph2, and Zfp769 in the depression mouse model (p < 0.05). Notably, Oprm1 exhibited the highest feature importance, contributing to a model accuracy of 94.5%. Gene expression patterns showed strong consistency across the prefrontal cortex (PFC) and nucleus accumbens (NAC). Conclusion: The combined application of machine learning and transcriptomic analysis effectively identified core neurobiological genes in a depression model. Genes including Oprm1 and BDNF demonstrated functional relevance in modulating neural activity and behavior, offering promising candidates for early diagnosis and individualized treatment of depression.
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For statistical analysis, independent samples t-tests (Student’s t-test) were used to evaluate the significance of group differences, such as between CUS and control groups, based on normalized gene expression values.
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The Random Forest model achieved 94.5% overall classification accuracy, with an AUC of 0.937, when distinguishing control from chronic unpredictable stress mice.
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The results showed that the model achieved a classification accuracy of 95% for the control group (Ctrl) and 94% for the CUS model group, with an overall classification accuracy of 94.5%.
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The area under the curve (AUC) reached 0.937, indicating strong predictive performance across varying classification thresholds.
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ing to elucidate neural characteristics in a mouse model of depression.
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m1, BDNF, Tph2, and Zfp769 in the depression mouse model (p < 0.05). Notably, Oprm1 exhibited the hig
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obiological characteristics of depression in mouse models. Integration of weighted gene co-expr
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Complete file
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Integration of weighted gene co-expression network analysis (WGCNA) with the random forest algorithm enabled the identification of critical genes strongly associated with depression onset, offering theoretical support and potential biomarkers for early diagnosis and precision treatment.\nMethods: Gene expression data from depression-related mouse models were obtained from public GEO datasets (e.g., GSE102556) and normalized using Z-score transformation. WGCNA was employed to construct gene co-expression networks and explore associations between modules and depression-like behavioral phenotypes. Depression-related gene modules were identified and subjected to feature selection using the random forest model. The biological relevance of selected genes was further assessed, and model accuracy was validated through performance evaluation.\nResults: Our findings revealed significant differential expression of genes such as Oprm1, BDNF, Tph2, and Zfp769 in the depression mouse model (p < 0.05). Notably, Oprm1 exhibited the highest feature importance, contributing to a model accuracy of 94.5%. Gene expression patterns showed strong consistency across the prefrontal cortex (PFC) and nucleus accumbens (NAC).\nConclusion: The combined application of machine learning and transcriptomic analysis effectively identified core neurobiological genes in a depression model. 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