Comparison of fMRI Features for Brain-Behavior Prediction

Poster No:

1116 

Submission Type:

Abstract Submission 

Authors:

Mikkel Schöttner1, Thomas Bolton1, Jagruti Patel1, Patric Hagmann2

Institutions:

1University of Lausanne, Lausanne, Vaud, 2Lausanne University Hospital and University of Lausanne (CHUV-UNIL), Lausanne, Vaud

First Author:

Mikkel Schöttner  
University of Lausanne
Lausanne, Vaud

Co-Author(s):

Thomas Bolton  
University of Lausanne
Lausanne, Vaud
Jagruti Patel  
University of Lausanne
Lausanne, Vaud
Patric Hagmann  
Lausanne University Hospital and University of Lausanne (CHUV-UNIL)
Lausanne, Vaud

Introduction:

Brain-behavior prediction enables the development of robust models of how the brain gives rise to our behavior, and is the first step in the development of neuroimaging biomarkers. However, many methodological choices need to be made in the processing pipeline. An important consideration is the choice of feature that is used to predict the behavior at hand. Functional connectivity (FC), is an established choice (He et al., 2020; Ooi et al., 2022), but regional measures of functional magnetic resonance imaging (fMRI) and those derived using graph signal processing (GSP), have also shown potential in modeling inter-individual differences (Brahim & Farrugia, 2020; Griffa et al., 2022). In addition to evaluating its predictive performance, varying the sample size and scan time available to train a model for a given feature can give an indication of potential performance reserves. At the same time, the choice between acquiring more subjects or scanning each subject for longer is important to explore in the context of prospective brain-behavior prediction studies (Ooi et al., 2024).

Methods:

We compared the prediction performance of 10 fMRI measures on 979 subjects from the Human Connectome Project Young Adult dataset (Van Essen et al., 2012), predicting cognition, age, and gender. We explored the comparative performance of FC, regional measures, and measures using GSP. The region-wise measures were mean, standard deviation, mean square successive difference (MSSD, Garrett et al., 2013), and fractional amplitude of low-frequency fluctuations (fALFF, Zou et al., 2008). The GSP-based measures were structural decoupling index (SDI, Preti & Van De Ville, 2019), power spectral density (PSD), and coupled and decoupled FC (Griffa et al., 2022). To test whether any differences in performance was due to the dimensionality of the feature, the first 274 principal components of FC were also included as a feature. Depending on the dimensionality of the feature and whether the target was continuous or discrete, we used elastic-net regression, kernel-ridge regression, elastic-net classifier, or support vector machine as our model. The model was evaluated in a nested cross-validation with 10 random splits. The scaling properties were explored by fitting the same models, varying the size of the training set and the number of scanning sessions.

Results:

Figure 1 shows the results of the feature comparison. FC-based measures came out best for all three targets. Standard deviation and MSSD also showed potential for predicting cognition, while PSD and SDI did relatively well in the age prediction. Coupled FC outperformed FC when predicting gender. Figure 2 shows the results of the scaling experiment. Both sample size and scan time were important for predicting each target. Prediction performance leveled off for a given scan time for cognition and gender, indicating that it places a limit on how well a model is able to perform.
Supporting Image: Figure1.png
Supporting Image: Figure2.png
 

Conclusions:

Our results confirm that FC represents a robust feature for brain-behavior prediction. They further illustrate the potential of GSP-based features and measures of variability for this task. Both scan time and sample size should be considered when planning data acquisition for brain-behavior prediction studies, with the former placing a limit on the maximum performance that can be achieved.

Higher Cognitive Functions:

Higher Cognitive Functions Other

Modeling and Analysis Methods:

Classification and Predictive Modeling 1
Connectivity (eg. functional, effective, structural) 2
fMRI Connectivity and Network Modeling

Novel Imaging Acquisition Methods:

BOLD fMRI

Keywords:

Cognition
Data analysis
FUNCTIONAL MRI
Machine Learning
MRI

1|2Indicates the priority used for review

Abstract Information

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Please indicate below if your study was a "resting state" or "task-activation” study.

Resting state

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

Healthy subjects

Was this research conducted in the United States?

No

Were any human subjects research approved by the relevant Institutional Review Board or ethics panel? NOTE: Any human subjects studies without IRB approval will be automatically rejected.

Yes

Were any animal research approved by the relevant IACUC or other animal research panel? NOTE: Any animal studies without IACUC approval will be automatically rejected.

Not applicable

Please indicate which methods were used in your research:

Functional MRI
Structural MRI
Diffusion MRI
Behavior

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

3.0T

Which processing packages did you use for your study?

FSL
Free Surfer

Provide references using APA citation style.

Brahim, A., & Farrugia, N. (2020). Graph Fourier transform of fMRI temporal signals based on an averaged structural connectome for the classification of neuroimaging. Artificial Intelligence in Medicine, 106, 101870.
Garrett, D. D., Samanez-Larkin, G. R., MacDonald, S. W. S., Lindenberger, U., McIntosh, A. R., & Grady, C. L. (2013). Moment-to-moment brain signal variability: A next frontier in human brain mapping? Neuroscience & Biobehavioral Reviews, 37(4), 610–624.
Griffa, A., Amico, E., Liégeois, R., Van De Ville, D., & Preti, M. G. (2022). Brain structure-function coupling provides signatures for task decoding and individual fingerprinting. NeuroImage, 250, 118970. https://doi.org/10.1016/j.neuroimage.2022.118970
He, T., Kong, R., Holmes, A. J., Nguyen, M., Sabuncu, M. R., Eickhoff, S. B., Bzdok, D., Feng, J., & Yeo, B. T. T. (2020). Deep neural networks and kernel regression achieve comparable accuracies for functional connectivity prediction of behavior and demographics. NeuroImage, 206, 116276.
Ooi, L. Q. R., Chen, J., Zhang, S., Kong, R., Tam, A., Li, J., Dhamala, E., Zhou, J. H., Holmes, A. J., & Yeo, B. T. T. (2022). Comparison of individualized behavioral predictions across anatomical, diffusion and functional connectivity MRI. NeuroImage, 263, 119636.
Ooi, L. Q. R., Orban, C., Nichols, T. E., Zhang, S., Tan, T. W. K., Kong, R., Marek, S., Dosenbach, N. U. F., Laumann, T., Gordon, E. M., Zhou, J. H., Bzdok, D., Eickhoff, S. B., Holmes, A. J., & Yeo, B. T. T. (2024). MRI economics: Balancing sample size and scan duration in brain wide association studies (p. 2024.02.16.580448). bioRxiv.
Preti, M. G., & Van De Ville, D. (2019). Decoupling of brain function from structure reveals regional behavioral specialization in humans. Nature Communications, 10(1), Article 1.
Van Essen, D. C., Ugurbil, K., Auerbach, E., Barch, D., Behrens, T. E. J., Bucholz, R., Chang, A., Chen, L., Corbetta, M., Curtiss, S. W., Della Penna, S., Feinberg, D., Glasser, M. F., Harel, N., Heath, A. C., Larson-Prior, L., Marcus, D., Michalareas, G., Moeller, S., … WU-Minn HCP Consortium. (2012). The Human Connectome Project: A data acquisition perspective. NeuroImage, 62(4), 2222–2231.
Zou, Q.-H., Zhu, C.-Z., Yang, Y., Zuo, X.-N., Long, X.-Y., Cao, Q.-J., Wang, Y.-F., & Zang, Y.-F. (2008). An improved approach to detection of amplitude of low-frequency fluctuation (ALFF) for resting-state fMRI: Fractional ALFF. Journal of Neuroscience Methods, 172(1), 137–141.

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