Enhancing Group-Level Discriminant fMRI Analysis with Independent Filter Analysis (IFA)

Poster No:

1457 

Submission Type:

Abstract Submission 

Authors:

Zain Souweidane1, Stephen Smith2, Christian Beckmann1

Institutions:

1Donders Institute for Brain, Cognition, and Behaviour, Nijmegen, Netherlands, 2University of Oxford, Oxford, Oxfordshire

First Author:

Zain Souweidane  
Donders Institute for Brain, Cognition, and Behaviour
Nijmegen, Netherlands

Co-Author(s):

Stephen Smith  
University of Oxford
Oxford, Oxfordshire
Christian Beckmann  
Donders Institute for Brain, Cognition, and Behaviour
Nijmegen, Netherlands

Introduction:

Group-level fMRI analysis, particularly group Independent Component Analysis (ICA) with dual regression (Nickerson et al., 2017), effectively captures biologically relevant spatial networks (RSNs). However, group ICA is limited by shared component bias, prioritizing commonalities over discriminative features. This limitation arises from the PCA-based projection of the data into a lower-dimensional space before ICA unmixing, which preserves bulk variance rather than group-discriminative features. This hinders downstream analyses, like classifying network matrices (netmats) from dual regression (Dadi et al., 2019). Independent Filter Analysis (IFA) addresses this by preserving group-discriminative information while maintaining biologically interpretable spatial networks.

Methods:

IFA identifies a spatial basis that preserves biologically meaningful networks and group-level differences in functional connectivity. To achieve this, MIGP (Smith et al., 2014) and Probabilistic Principal Component Analysis (PPCA) (Beckmann & Smith, 2004) are applied to extract a basis representing functional spatial networks. TSSF (Xu et al., 2020) or SPADE (Llera et al., 2020) is used to identify discriminative components that maximize group-level differences in functional connectivity. TSSF is ideal for parcellated data, providing robust and flexible classification of group differences, while SPADE can generalize this approach to voxel data, making it suitable for higher-resolution analyses. If discrimination is done in a parcellated space, the discriminant filters are projected to voxel space via dual regression (Nickerson et al., 2017). The PPCA and discriminative bases are then combined and unmixed using ICA. Following ICA, dual regression is applied again to generate individual-level spatial maps and netmats. The full IFA pipeline is visualized in Figure 1.

To assess IFA's ability to preserve group differences, the subject-wise netmats are mapped into a tangent space, centered on the mean netmats from the training group (last step in Figure 1). Group separability is quantified using various machine learning classifiers, with classification accuracy providing an empirical measure of discriminability (Pervaiz et al., 2020). A tangent-space t-test is performed on the netmats to identify statistically significant group differences in connectivity (Varoquaux et al., 2010).
Supporting Image: Figure1Label.png
 

Results:

The Human Connectome Project (HCP) dataset (Glasser et al., 2013) was used to evaluate IFA against group ICA across three scenarios: simulated two-group differences embedded into resting-state data, between-task differences (e.g., working memory vs. motor) in the HCP task FMRI data, and within-task differences (e.g., 0-back vs. 2-back working memory). IFA consistently enhanced group-level discrimination while preserving biologically interpretable networks. The degree of improvement depended on the inherent separability of the groups and the total number of PCA components used in the analysis. For large between-task differences, IFA achieved modest gains in netmat classification accuracy. However, for more subtle within-task differences, such as 0-back faces vs. 2-back faces, IFA substantially improved classification accuracy, increasing performance by 9% (Figure 2a)-from 87% (ICA with 10 PCA components) to 96% (IFA with 6 PCA components and 4 discriminant components). Additionally, IFA identified 35 statistically significant connectivity differences in tangent-space t-tests, compared to 26 for ICA (Figure 2b), highlighting its improved ability to detect interpretable group-level differences in functional connectivity.
Supporting Image: Figure2Label.png
 

Conclusions:

IFA addresses shared component bias in group ICA by retaining group-discriminative features while preserving the ability to extract biologically interpretable networks (RSNs). By improving classification accuracy and enabling the detection of group differences in netmats, IFA offers a robust approach for identifying meaningful group-level variations in functional connectivity.

Modeling and Analysis Methods:

Classification and Predictive Modeling 2
Connectivity (eg. functional, effective, structural)
fMRI Connectivity and Network Modeling 1
Methods Development
Task-Independent and Resting-State Analysis

Keywords:

Data analysis
FUNCTIONAL MRI
Machine Learning
Multivariate
Statistical Methods

1|2Indicates the priority used for review

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Healthy subjects only or patients (note that patient studies may also involve healthy subjects):

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Was this research conducted in the United States?

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Please indicate which methods were used in your research:

Functional MRI
Computational modeling

For human MRI, what field strength scanner do you use?

3.0T

Which processing packages did you use for your study?

FSL

Provide references using APA citation style.

1. Beckmann, C. F. (2004). Probabilistic independent component analysis for functional magnetic resonance imaging. IEEE Transactions on Medical Imaging, 23(2), 137–152. https://doi.org/10.1109/TMI.2003.822821

2. Dadi, K. (2019). Benchmarking functional connectome-based predictive models for resting-state fMRI. NeuroImage, 192, 115–134. https://doi.org/10.1016/j.neuroimage.2019.02.062

3. Glasser, M. F. (2013). The minimal preprocessing pipelines for the Human Connectome Project. NeuroImage, 80, 105–124. https://doi.org/10.1016/j.neuroimage.2013.04.127

4. Llera, A. (2020). Spatial Patterns for Discriminative Estimation (p. 746891). bioRxiv. https://doi.org/10.1101/746891

5. Nickerson, L. D. (2017). Using Dual Regression to Investigate Network Shape and Amplitude in Functional Connectivity Analyses. Frontiers in Neuroscience, 11. https://doi.org/10.3389/fnins.2017.00115

6. Pervaiz, U. (2020). Optimising network modelling methods for fMRI. NeuroImage, 211, 116604. https://doi.org/10.1016/j.neuroimage.2020.116604

7. Smith, S. M. (2014). Group-PCA for very large fMRI datasets. NeuroImage, 101, 738–749. https://doi.org/10.1016/j.neuroimage.2014.07.051

8. Varoquaux, G. (2010). Detection of Brain Functional-Connectivity Difference in Post-stroke Patients Using Group-Level Covariance Modeling. In T. Jiang, N. Navab, J. P. W. Pluim, & M. A. Viergever (Eds.), Medical Image Computing and Computer-Assisted Intervention – MICCAI 2010 (pp. 200–208). Springer. https://doi.org/10.1007/978-3-642-15705-9_25

9. Xu, J. (2020). Tangent space spatial filters for interpretable and efficient Riemannian classification. Journal of Neural Engineering, 17(2), 026043. https://doi.org/10.1088/1741-2552/ab839e

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