Meta‐Analysis Informed Functional Connectomes Representations for Depression Identification

ABSTRACT Background Meta‐analyses in neuroimaging have gained popularity. However, their clinical utility remains uncertain. Convergent masks, containing repeated clusters from publications, are often focal and small, and voxel‐wise features can lead to the curse of dimensionality, limiting discrimi...

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Published inJournal of magnetic resonance imaging Vol. 62; no. 5; pp. 1358 - 1368
Main Authors Wang, Xinyi, Xue, Li, Dai, Zhongpeng, Shao, Junneng, Zhang, Yujie, Tian, Shui, Yan, Rui, Chen, Zhilu, Yao, Zhijian, Lu, Qing
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.11.2025
Wiley Subscription Services, Inc
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ISSN1053-1807
1522-2586
1522-2586
DOI10.1002/jmri.29801

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Abstract ABSTRACT Background Meta‐analyses in neuroimaging have gained popularity. However, their clinical utility remains uncertain. Convergent masks, containing repeated clusters from publications, are often focal and small, and voxel‐wise features can lead to the curse of dimensionality, limiting discriminative ability in clinical diagnosis. Purpose To develop a functional connectome representation (FCR) by integrating meta‐analytic neuroimaging data and to evaluate its performance in identifying depression. Study Type Retrospective. Subjects The principal data set included 151 patients with depression (male/female, 72/79) and 105 healthy controls (male/female, 48/57). An external test data set comprised 109 patients (male/female, 44/65) and 54 healthy controls (male/female, 15/39). Field Strength/Sequence 3.0 T T1‐weighted imaging, resting‐state functional MRI with echo‐planar sequence. Assessment We performed the community detection algorithm and principal component analysis to develop the FCR. The model's performance based on the FCR was evaluated in terms of accuracy, specificity, and sensitivity. Effect sizes (Cohen's d) for FCR components were calculated between patients and healthy controls. Model robustness was assessed by analyzing the association between accuracy and the degree of shuffled features in the permutation test. Statistical Tests Chi‐squared test, two‐sample t‐test, effect sizes (Cohen's d), permutation tests for accuracy validation, and correlation analysis. Significance was determined at p < 0.05. Results Effect sizes (Cohen's d) for each of the 39 principal components to quantify the magnitude of differences between depressed patients and healthy controls, ranged from d = −0.22 to d = 0.84. The FCR‐based diagnostic model achieved an accuracy of 89.42% (principal data set) and 83.35% (external data set). Permutation tests (n = 1000) indicated that the model's accuracy was significantly higher than chance level. A significant negative correlation was observed between random noise and accuracy (r = −0.093). Data Conclusion The FCR effectively discriminates between depressed patients and healthy controls, exhibiting strong diagnostic performance, generalization, and robustness, supporting its potential utility in clinical depression identification. Evidence Level Level 3. Technical Efficacy Stage 2.
AbstractList ABSTRACT Background Meta‐analyses in neuroimaging have gained popularity. However, their clinical utility remains uncertain. Convergent masks, containing repeated clusters from publications, are often focal and small, and voxel‐wise features can lead to the curse of dimensionality, limiting discriminative ability in clinical diagnosis. Purpose To develop a functional connectome representation (FCR) by integrating meta‐analytic neuroimaging data and to evaluate its performance in identifying depression. Study Type Retrospective. Subjects The principal data set included 151 patients with depression (male/female, 72/79) and 105 healthy controls (male/female, 48/57). An external test data set comprised 109 patients (male/female, 44/65) and 54 healthy controls (male/female, 15/39). Field Strength/Sequence 3.0 T T1‐weighted imaging, resting‐state functional MRI with echo‐planar sequence. Assessment We performed the community detection algorithm and principal component analysis to develop the FCR. The model's performance based on the FCR was evaluated in terms of accuracy, specificity, and sensitivity. Effect sizes (Cohen's d) for FCR components were calculated between patients and healthy controls. Model robustness was assessed by analyzing the association between accuracy and the degree of shuffled features in the permutation test. Statistical Tests Chi‐squared test, two‐sample t‐test, effect sizes (Cohen's d), permutation tests for accuracy validation, and correlation analysis. Significance was determined at p < 0.05. Results Effect sizes (Cohen's d) for each of the 39 principal components to quantify the magnitude of differences between depressed patients and healthy controls, ranged from d = −0.22 to d = 0.84. The FCR‐based diagnostic model achieved an accuracy of 89.42% (principal data set) and 83.35% (external data set). Permutation tests (n = 1000) indicated that the model's accuracy was significantly higher than chance level. A significant negative correlation was observed between random noise and accuracy (r = −0.093). Data Conclusion The FCR effectively discriminates between depressed patients and healthy controls, exhibiting strong diagnostic performance, generalization, and robustness, supporting its potential utility in clinical depression identification. Evidence Level Level 3. Technical Efficacy Stage 2.
Background Meta‐analyses in neuroimaging have gained popularity. However, their clinical utility remains uncertain. Convergent masks, containing repeated clusters from publications, are often focal and small, and voxel‐wise features can lead to the curse of dimensionality, limiting discriminative ability in clinical diagnosis. Purpose To develop a functional connectome representation (FCR) by integrating meta‐analytic neuroimaging data and to evaluate its performance in identifying depression. Study Type Retrospective. Subjects The principal data set included 151 patients with depression (male/female, 72/79) and 105 healthy controls (male/female, 48/57). An external test data set comprised 109 patients (male/female, 44/65) and 54 healthy controls (male/female, 15/39). Field Strength/Sequence 3.0 T T1‐weighted imaging, resting‐state functional MRI with echo‐planar sequence. Assessment We performed the community detection algorithm and principal component analysis to develop the FCR. The model's performance based on the FCR was evaluated in terms of accuracy, specificity, and sensitivity. Effect sizes (Cohen's d) for FCR components were calculated between patients and healthy controls. Model robustness was assessed by analyzing the association between accuracy and the degree of shuffled features in the permutation test. Statistical Tests Chi‐squared test, two‐sample t‐test, effect sizes (Cohen's d), permutation tests for accuracy validation, and correlation analysis. Significance was determined at p < 0.05. Results Effect sizes (Cohen's d) for each of the 39 principal components to quantify the magnitude of differences between depressed patients and healthy controls, ranged from d = −0.22 to d = 0.84. The FCR‐based diagnostic model achieved an accuracy of 89.42% (principal data set) and 83.35% (external data set). Permutation tests (n = 1000) indicated that the model's accuracy was significantly higher than chance level. A significant negative correlation was observed between random noise and accuracy (r = −0.093). Data Conclusion The FCR effectively discriminates between depressed patients and healthy controls, exhibiting strong diagnostic performance, generalization, and robustness, supporting its potential utility in clinical depression identification. Evidence Level Level 3. Technical Efficacy Stage 2.
Meta-analyses in neuroimaging have gained popularity. However, their clinical utility remains uncertain. Convergent masks, containing repeated clusters from publications, are often focal and small, and voxel-wise features can lead to the curse of dimensionality, limiting discriminative ability in clinical diagnosis. To develop a functional connectome representation (FCR) by integrating meta-analytic neuroimaging data and to evaluate its performance in identifying depression. Retrospective. The principal data set included 151 patients with depression (male/female, 72/79) and 105 healthy controls (male/female, 48/57). An external test data set comprised 109 patients (male/female, 44/65) and 54 healthy controls (male/female, 15/39). 3.0 T T1-weighted imaging, resting-state functional MRI with echo-planar sequence. We performed the community detection algorithm and principal component analysis to develop the FCR. The model's performance based on the FCR was evaluated in terms of accuracy, specificity, and sensitivity. Effect sizes (Cohen's d) for FCR components were calculated between patients and healthy controls. Model robustness was assessed by analyzing the association between accuracy and the degree of shuffled features in the permutation test. Chi-squared test, two-sample t-test, effect sizes (Cohen's d), permutation tests for accuracy validation, and correlation analysis. Significance was determined at p < 0.05. Effect sizes (Cohen's d) for each of the 39 principal components to quantify the magnitude of differences between depressed patients and healthy controls, ranged from d = -0.22 to d = 0.84. The FCR-based diagnostic model achieved an accuracy of 89.42% (principal data set) and 83.35% (external data set). Permutation tests (n = 1000) indicated that the model's accuracy was significantly higher than chance level. A significant negative correlation was observed between random noise and accuracy (r = -0.093). The FCR effectively discriminates between depressed patients and healthy controls, exhibiting strong diagnostic performance, generalization, and robustness, supporting its potential utility in clinical depression identification. Level 3. Stage 2.
Meta-analyses in neuroimaging have gained popularity. However, their clinical utility remains uncertain. Convergent masks, containing repeated clusters from publications, are often focal and small, and voxel-wise features can lead to the curse of dimensionality, limiting discriminative ability in clinical diagnosis.BACKGROUNDMeta-analyses in neuroimaging have gained popularity. However, their clinical utility remains uncertain. Convergent masks, containing repeated clusters from publications, are often focal and small, and voxel-wise features can lead to the curse of dimensionality, limiting discriminative ability in clinical diagnosis.To develop a functional connectome representation (FCR) by integrating meta-analytic neuroimaging data and to evaluate its performance in identifying depression.PURPOSETo develop a functional connectome representation (FCR) by integrating meta-analytic neuroimaging data and to evaluate its performance in identifying depression.Retrospective.STUDY TYPERetrospective.The principal data set included 151 patients with depression (male/female, 72/79) and 105 healthy controls (male/female, 48/57). An external test data set comprised 109 patients (male/female, 44/65) and 54 healthy controls (male/female, 15/39).SUBJECTSThe principal data set included 151 patients with depression (male/female, 72/79) and 105 healthy controls (male/female, 48/57). An external test data set comprised 109 patients (male/female, 44/65) and 54 healthy controls (male/female, 15/39).3.0 T T1-weighted imaging, resting-state functional MRI with echo-planar sequence.FIELD STRENGTH/SEQUENCE3.0 T T1-weighted imaging, resting-state functional MRI with echo-planar sequence.We performed the community detection algorithm and principal component analysis to develop the FCR. The model's performance based on the FCR was evaluated in terms of accuracy, specificity, and sensitivity. Effect sizes (Cohen's d) for FCR components were calculated between patients and healthy controls. Model robustness was assessed by analyzing the association between accuracy and the degree of shuffled features in the permutation test.ASSESSMENTWe performed the community detection algorithm and principal component analysis to develop the FCR. The model's performance based on the FCR was evaluated in terms of accuracy, specificity, and sensitivity. Effect sizes (Cohen's d) for FCR components were calculated between patients and healthy controls. Model robustness was assessed by analyzing the association between accuracy and the degree of shuffled features in the permutation test.Chi-squared test, two-sample t-test, effect sizes (Cohen's d), permutation tests for accuracy validation, and correlation analysis. Significance was determined at p < 0.05.STATISTICAL TESTSChi-squared test, two-sample t-test, effect sizes (Cohen's d), permutation tests for accuracy validation, and correlation analysis. Significance was determined at p < 0.05.Effect sizes (Cohen's d) for each of the 39 principal components to quantify the magnitude of differences between depressed patients and healthy controls, ranged from d = -0.22 to d = 0.84. The FCR-based diagnostic model achieved an accuracy of 89.42% (principal data set) and 83.35% (external data set). Permutation tests (n = 1000) indicated that the model's accuracy was significantly higher than chance level. A significant negative correlation was observed between random noise and accuracy (r = -0.093).RESULTSEffect sizes (Cohen's d) for each of the 39 principal components to quantify the magnitude of differences between depressed patients and healthy controls, ranged from d = -0.22 to d = 0.84. The FCR-based diagnostic model achieved an accuracy of 89.42% (principal data set) and 83.35% (external data set). Permutation tests (n = 1000) indicated that the model's accuracy was significantly higher than chance level. A significant negative correlation was observed between random noise and accuracy (r = -0.093).The FCR effectively discriminates between depressed patients and healthy controls, exhibiting strong diagnostic performance, generalization, and robustness, supporting its potential utility in clinical depression identification.DATA CONCLUSIONThe FCR effectively discriminates between depressed patients and healthy controls, exhibiting strong diagnostic performance, generalization, and robustness, supporting its potential utility in clinical depression identification.Level 3.EVIDENCE LEVELLevel 3.Stage 2.TECHNICAL EFFICACYStage 2.
Author Zhang, Yujie
Yao, Zhijian
Wang, Xinyi
Dai, Zhongpeng
Xue, Li
Tian, Shui
Chen, Zhilu
Shao, Junneng
Yan, Rui
Lu, Qing
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Keywords functional connectomes representation
depression
meta‐analysis
machine learning framework
resting‐state magnetic resonance imaging
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This work was supported by the National Natural Science Foundation of China (82151315, 82271568, 82101573, 82301718, 82401788), Jiangsu Provincial Medical Innovation Team of the Project of Invigorating Health Care through Science, Technology and Education (CXTDC2016004), Jiangsu Provincial Key Research and Development Program (BE2019675), Key Project Supported by Medical Science and Technology Development Foundation, Jiangsu Commission of Health (K2019011), the Fundamental Research Funds for the Center Universities (2242021k30014), Nanjing Normal University Research Start‐up Funding (184080H201A102), Key Project of Science and Technology Innovation for Social Development in Suzhou (2022SS04), and Jiangsu Provincial Natural Science Youth Fund (BK20230154).
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Snippet ABSTRACT Background Meta‐analyses in neuroimaging have gained popularity. However, their clinical utility remains uncertain. Convergent masks, containing...
Meta-analyses in neuroimaging have gained popularity. However, their clinical utility remains uncertain. Convergent masks, containing repeated clusters from...
Background Meta‐analyses in neuroimaging have gained popularity. However, their clinical utility remains uncertain. Convergent masks, containing repeated...
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StartPage 1358
SubjectTerms Accuracy
Adult
Algorithms
Brain - diagnostic imaging
Brain - physiopathology
Cohen's d
Connectome - methods
Correlation analysis
Datasets
depression
Depression - diagnostic imaging
Female
Females
Field strength
functional connectomes representation
Functional magnetic resonance imaging
Humans
Image Processing, Computer-Assisted
machine learning framework
Magnetic Resonance Imaging - methods
Male
Males
Medical imaging
Mental depression
Meta-analysis
Middle Aged
Neuroimaging
Neuroimaging - methods
Performance evaluation
Permutations
Principal Component Analysis
Principal components analysis
Random noise
Representations
Reproducibility of Results
resting‐state magnetic resonance imaging
Retrospective Studies
Robust control
Sensitivity and Specificity
Statistical analysis
Statistical tests
Title Meta‐Analysis Informed Functional Connectomes Representations for Depression Identification
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjmri.29801
https://www.ncbi.nlm.nih.gov/pubmed/40260912
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https://www.proquest.com/docview/3193711630
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