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 in | Journal of magnetic resonance imaging Vol. 62; no. 5; pp. 1358 - 1368 | 
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| Main Authors | , , , , , , , , , | 
| Format | Journal Article | 
| Language | English | 
| Published | 
        Hoboken, USA
          John Wiley & Sons, Inc
    
        01.11.2025
     Wiley Subscription Services, Inc  | 
| Subjects | |
| Online Access | Get full text | 
| ISSN | 1053-1807 1522-2586 1522-2586  | 
| DOI | 10.1002/jmri.29801 | 
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| Summary: | 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. | 
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| Bibliography: | Funding 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). ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23  | 
| ISSN: | 1053-1807 1522-2586 1522-2586  | 
| DOI: | 10.1002/jmri.29801 |