Poster No:
1456
Submission Type:
Abstract Submission
Authors:
Julian Ramirez1, Robert Hermosillo2, Julia Moser3, Gracie Grimsrud1, Erendiz Tarakci1, Hannah Pham1, Vanessa Morgan1, Thomas Madison1, Kimberly Weldon1, Oscar Miranda-Dominguez1, Brenden Tervo-Clemmens1, Steven Nelson1, Damien Fair1
Institutions:
1University of Minnesota, Minneapolis, MN, 2Oregon Health & Science University, Portland, OR, 3Masonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN
First Author:
Co-Author(s):
Julia Moser, PhD
Masonic Institute for the Developing Brain, University of Minnesota
Minneapolis, MN
Introduction:
There has been a shift in resting-state, rs-fMRI from relying on group-averaged functional network topographies toward subject-specific configurations derived from densely sampled scans. Although existing approaches can identify networks within individual participants (e.g., Hermosillo et al. 2024; Laumann et al. 2015), they yield categorical network assignments that do not estimate uncertainty and measurement error. In scenarios demanding precise, individualized network localization-such as neuromodulation-categorical-only labels become problematic for subjects with limited data. This underscores the need for confidence measures, as smaller datasets with short acquisitions (common in clinical applications) yield less stable network assignments that compromise reliability.
Methods:
We introduce Precision Confidence Mapping (PCM), an extension of network-detection methods that provides individualized functional network topographies and their confidence maps. PCM leverages the temporal nature of rs-fMRI data by bootstrapping volumes (e.g., n=100 iterations) into new, shuffled time series of a user-defined length. A community detection algorithm is applied to each bootstrap iteration, yielding a probability of network assignments for each grayordinate. Assignments are aggregated across permutations to produce "confidence maps" that estimate network stability across iterations. This framework enables analyses of individual-specific functional networks and facilitates analyses of network stability, data requirements, and assignment probabilities. Further, confidence maps can be thresholded, enabling researchers to identify regions with differing degrees of assignment certainty.
Results:
We validated PCM on four adults, each contributing 140 minutes of low-motion (FD<0.2mm) multi-band, multi-echo rsfMRI data. Each dataset was divided into two 70-minute halves: one served as a "ground truth" validation, while the other ("exploratory") was split into bins ranging from 2 to 70 minutes to examine the effect of rs-fMRI duration on confidence maps. We examined both dice coefficients and positive predictive value (PPV) between the exploratory bins and ground truth to assess spatial overlap versus assignment accuracy. With short durations, PCM reveals network assignments with moderate to high uncertainty, which decreases as dataset length increases. Unthresholded confidence maps showed dice coefficients increased from 0.26±0.13 at 2 minutes to 0.74±0.08 at 70 minutes. Applying thresholds to confidence maps (Figure 1A & D) revealed that lower thresholds (10–30%) yielded higher dice scores (e.g., 0.48±0.08 at 2 minutes and 0.75±0.07 at 70 minutes). However, as thresholds increased this dice score recovery declined (Figure 1C). To capture how accurately each thresholded exploratory map aligned with ground truth network labels, we calculated PPV (Figure 1E). For a 10% threshold at 2 minutes, the mean PPV was 0.52±0.13, rising to 0.77±0.10 at 70 minutes. However, a 90% threshold at 2 minutes yielded a higher PPV of 0.85±0.12, more closely matching the 70-minute bin (0.78±0.11). This underscores how thresholding retains accurate vertices in short, variable datasets, while minimally affecting stable assignments at longer durations. These results suggest that while lower thresholds improve overall spatial overlap (dice), higher thresholds increase accuracy (PPV) of identified regions, which could be crucial for targeted interventions.

·Precision confidence maps illustrating how data length and thresholding improve assignment stability and accuracy.
Conclusions:
These findings illustrate how PCM refines individualized network identification by quantifying stability for both data quantity and confidence thresholds. Unlike purely binary assignment methods, PCM offers a tunable measure of certainty that can inform precision interventions (e.g., Deep Brain Stimulation, Transcranial Magnetic Stimulation) and refine minimum data requirements for reliable network mapping. As PCM evolves, it promises to integrate precise neuroscientific insights into personalized therapies.
Brain Stimulation:
Non-Invasive Stimulation Methods Other 2
Modeling and Analysis Methods:
fMRI Connectivity and Network Modeling 1
Segmentation and Parcellation
Neuroanatomy, Physiology, Metabolism and Neurotransmission:
Cortical Anatomy and Brain Mapping
Novel Imaging Acquisition Methods:
BOLD fMRI
Keywords:
Computational Neuroscience
Cortex
Data analysis
Design and Analysis
FUNCTIONAL MRI
Informatics
Segmentation
Statistical Methods
Systems
Transcranial Magnetic Stimulation (TMS)
1|2Indicates the priority used for review
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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?
Yes
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Yes, I have IRB or AUCC approval
Were any human subjects research approved by the relevant Institutional Review Board or ethics panel?
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Yes
Were any animal research approved by the relevant IACUC or other animal research panel?
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Not applicable
Please indicate which methods were used in your research:
Functional MRI
Structural 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
Free Surfer
Provide references using APA citation style.
Laumann, T. O., Gordon, E. M., Adeyemo, B., Snyder, A. Z., Joo, S. J., Chen, M.-Y., Gilmore, A. W., McDermott, K. B., Nelson, S. M., Dosenbach, N. U. F., Schlaggar, B. L., Mumford, J. A., Poldrack, R. A., & Petersen, S. E. (2015). Functional system and areal organization of a highly sampled individual human brain. Neuron, 87(3), 657–670.
Hermosillo, R. J. M., Moore, L. A., Feczko, E., Miranda-Domínguez, Ó., Pines, A., Dworetsky, A., Conan, G., Mooney, M. A., Randolph, A., Graham, A., Adeyemo, B., Earl, E., Perrone, A., Morales Carrasco, C., Uriarte-Lopez, J., Snider, K., Doyle, O., Cordova, M., Koirala, S., … Fair, D. A. (2024). A precision functional atlas of personalized network topography and probabilities. Nature Neuroscience, 27, 1000–1013.
No