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BrainOOD: Out-of-distribution Generalizable Brain Network Analysis
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Proposes BrainOOD, a GIB-based GNN with feature masking, high-pass reconstruction, discrete edge sampling and an alignment loss for OOD-generalizable and interpretable brain network classification, plus the first site-holdout OOD brain network benchmark on ABIDE and ADNI.
Problem
Brain network classifiers degrade under multi-site distribution shifts when applied to unseen sites, and existing graph OOD/causal-subgraph methods ignore node-feature noise and fail to give consistent, interpretable ROI selections for neurological disorders.
Approach
Extends the graph information bottleneck with a learnable node-feature mask trained by reconstruction through a high-pass GNN, discrete Gumbel-based edge sampling for subgraph extraction, and an alignment loss that encourages the same connections to be selected across all brain networks in a batch.
Key results
- BrainOOD achieves 64.81% OOD accuracy on ABIDE versus 60.38% for the best baseline (BrainNetCNN), a 7.34% relative gain as reported in the text.
- On ADNI 6-class, BrainOOD reaches 64.07% OOD accuracy and 64.80% overall accuracy, the best among compared methods.
- Ablation on ABIDE shows removing the entropy, reconstruction, or alignment loss, or using unmasked features or the original adjacency, lowers overall accuracy from 63.95% to between 60.10% and 63.12%.
Measured effects reported in the paper
| What was changed | Where | Measured | Effect |
|---|---|---|---|
| Apply BrainOOD with the GIN backbone rather than the strongest listed baseline | ABIDE OOD classification · ABIDE OOD | accuracy: 60.38 ± 7.07 -> 64.81 ± 9.01 | Helped |
| Apply BrainOOD with the GIN backbone rather than the strongest listed baseline | ADNI 5-class OOD classification · ADNI 5-class OOD | accuracy: 60.93 ± 13.27 -> 62.26 ± 15.83 | Helped |
| Apply BrainOOD with the GIN backbone rather than the strongest listed baseline | ADNI 6-class OOD classification · ADNI 6-class OOD | accuracy: 60.79 ± 13.97 -> 64.07 ± 14.99 | Helped |
| Add entropy loss (ablation) | BrainOOD on ABIDE · ABIDE | OOD accuracy: 63.70 ± 4.53 -> 64.81 ± 9.01 | Helped |
| Add reconstruction loss (ablation) | BrainOOD on ABIDE · ABIDE | OOD accuracy: 61.37 ± 7.13 -> 64.81 ± 9.01 | Helped |
| Add alignment loss (ablation) | BrainOOD on ABIDE · ABIDE | OOD accuracy: 60.43 ± 5.45 -> 64.81 ± 9.01 | Helped |
| Use masked features X' rather than unmasked features X (ablation) | BrainOOD on ABIDE · ABIDE | OOD accuracy: 62.26 ± 5.68 -> 64.81 ± 9.01 | Helped |
| Use sampled adjacency A' rather than original adjacency A (ablation) | BrainOOD on ABIDE · ABIDE | OOD accuracy: 55.40 ± 8.95 -> 64.81 ± 9.01 | Helped |
| Use the selected hyperparameters k=5, λ1=0.01, λ2=0.1, λ3=0.5 instead of k=1 (ablation) | BrainOOD on ABIDE · ABIDE | overall accuracy: 61.95 ± 4.54 -> 63.95 ± 4.65 | Helped |
| Increase sampling count from k=5 to k=10 (ablation) | BrainOOD on ABIDE · ABIDE | overall accuracy: 63.95 ± 4.65 -> 62.90 ± 4.67 | Hurt |
| Increase sampling count from k=5 to k=20 (ablation) | BrainOOD on ABIDE · ABIDE | overall accuracy: 63.95 ± 4.65 -> 61.59 ± 3.57 | Hurt |
| Set λ2 to 1.0 rather than the selected 0.1 (ablation) | BrainOOD on ABIDE · ABIDE | overall accuracy: 63.95 ± 4.65 -> 61.15 ± 2.84 | Hurt |
Surprising findings
- Most graph OOD methods (Mixup, DIR, GSAT, GMT) perform no better than ERM or simple GNN baselines on brain networks.
- Existing graph OOD methods with a GCN backbone fail to improve over the plain GCN baseline.
Limitations
- Reported OOD gains have large standard deviations, so differences between methods are often within noise.
- Evaluation uses only two brain network datasets (ABIDE and ADNI) with Schaefer-100 fMRI connectivity.
Experimental setup
Datasets: ABIDE ADNI
Benchmarks: ABIDE ADNI
Metrics: accuracy precision recall micro-F1 ROC-AUC
Baselines: ERM Deep Coral IRM GroupDRO VREx Mixup DIR GSAT GMT GCN GIN GAT
Builds on: GSAT GIB DIR GMT GOOD
Closest papers by meaning
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- Benchmarking Out-of-Distribution Generalization Capabilities of DNN-based Encoding Models for the Ventral Visual Cortex. (NeurIPS 2024 · similarity 0.84)
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