Poster No:
1167
Submission Type:
Abstract Submission
Authors:
Xin Di1, Pratik Jain1, Bharat Biswal1
Institutions:
1New Jersey Institute of Technology, Newark, NJ
First Author:
Xin Di
New Jersey Institute of Technology
Newark, NJ
Co-Author(s):
Pratik Jain
New Jersey Institute of Technology
Newark, NJ
Introduction:
Research on brain functional connectivity frequently examines intra-individual, moment-to-moment correlations of functional activity, primarily using functional MRI (fMRI). Inter-individual correlations have also been analyzed using data from both fMRI (Taylor et al., 2012) and positron emission tomography (PET)(Di et al., 2017; Di & Biswal, and Alzheimer's Disease Neu, 2012). Many studies utilize a "resting-state" condition, where participants are scanned without being assigned specific tasks. This approach raises questions about how task conditions might influence inter-individual correlation estimates. Specifically, it remains uncertain how various tasks affect functional covariance measures of connectivity. Drawing on earlier findings that within-individual functional connectivity patterns are largely consistent across tasks (Cole et al., 2014), we hypothesized that functional covariance connectivity would similarly exhibit stability across different task conditions.
Methods:
We analyzed fMRI data from the 100 unrelated participants in the Human Connectome Project (HCP) (Barch et al., 2013), focusing on resting-state and six task conditions. The tasks included emotion, gambling, language, motor, relational, social, and working memory. Regional homogeneity (ReHo), a regional functional measure (Taylor et al., 2012; Zang et al., 2004) , was calculated for each task and resting-state run. The analysis utilized 114 regions of interest (ROIs) spanning cortical areas (Schaefer et al., 2018) and subcortical regions (Tzourio-Mazoyer et al., 2002).
For each task/rest condition, average ReHo values were extracted for each ROI, and inter-individual correlation coefficients were computed across the 114 ROIs, yielding a 114 x 114 covariance matrix. To evaluate the similarity of inter-individual correlation matrices across conditions, we calculated correlation coefficients between ROI pairs under different task/rest conditions. Additionally, repeated-measures analysis of variance (ANOVA) was performed to assess differences in correlations among the task and resting-state conditions.
Results:
The inter-individual correlation matrices for different task and resting-state conditions are presented in Figure 1. Whole-brain inter-individual correlation patterns were strikingly similar across tasks, with correlations exceeding 0.78. However, the resting-state condition exhibited the lowest correlations with the task conditions.
A repeated-measures ANOVA identified ROI pairs with significantly different connectivity across task conditions. The task-modulated connections were primarily concentrated within the visual network, somatomotor network, control network, and interactions among these networks. Comparisons between task conditions and the resting-state condition revealed consistent patterns across tasks (Figure 2). Specifically, connectivity within visual and somatomotor regions was generally lower during tasks, while connectivity between visual/somatomotor regions and control or subcortical regions was higher in task conditions compared with the resting-state condition.

·Figure 1

·Figure 2
Conclusions:
The connectivity matrices derived from inter-individual correlations of ReHo were highly consistent across different task conditions, aligning with previous findings on within-individual functional connectivity (Cole et al., 2014). However, subtle but significant differences in functional connectivity were observed, likely reflecting the involvement of specific brain regions associated with the tasks studied. Future research should account for task design when investigating inter-individual connectivity within specific brain systems.
Modeling and Analysis Methods:
Connectivity (eg. functional, effective, structural) 1
fMRI Connectivity and Network Modeling 2
Keywords:
FUNCTIONAL MRI
NORMAL HUMAN
Other - inter-individual correlation
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
Task-activation
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
Are you Internal Review Board (IRB) certified?
Please note: Failure to have IRB, if applicable will lead to automatic rejection of abstract.
Not applicable
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.
No
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.
No
Please indicate which methods were used in your research:
Functional MRI
For human MRI, what field strength scanner do you use?
3.0T
Which processing packages did you use for your study?
SPM
Provide references using APA citation style.
Barch, D. M., Burgess, G. C., Harms, M. P., Petersen, S. E., Schlaggar, B. L., Corbetta, M., Glasser, M. F., Curtiss, S., Dixit, S., Feldt, C., Nolan, D., Bryant, E., Hartley, T., Footer, O., Bjork, J. M., Poldrack, R., Smith, S., Johansen-Berg, H., Snyder, A. Z., & Van Essen, D. C. (2013). Function in the human connectome: Task-fMRI and individual differences in behavior. NeuroImage, 80, 169–189. https://doi.org/10.1016/j.neuroimage.2013.05.033
Cole, M. W., Bassett, D. S., Power, J. D., Braver, T. S., & Petersen, S. E. (2014). Intrinsic and task-evoked network architectures of the human brain. Neuron, 83, 238–251. https://doi.org/10.1016/j.neuron.2014.05.014
Di, X., & Biswal, and Alzheimer’s Disease Neu, B. B. (2012). Metabolic Brain Covariant Networks as Revealed by FDG-PET with Reference to Resting-State fMRI Networks. Brain Connectivity, 2(5), 275–283. https://doi.org/10.1089/brain.2012.0086
Di, X., Gohel, S., Thielcke, A., Wehrl, H. F., Biswal, B. B., & Alzheimer’s Disease Neuroimaging Initiative. (2017). Do all roads lead to Rome? A comparison of brain networks derived from inter-subject volumetric and metabolic covariance and moment-to-moment hemodynamic correlations in old individuals. Brain Structure & Function, 222(8), 3833–3845. https://doi.org/10.1007/s00429-017-1438-7
Schaefer, A., Kong, R., Gordon, E. M., Laumann, T. O., Zuo, X.-N., Holmes, A. J., Eickhoff, S. B., & Yeo, B. T. T. (2018). Local-Global Parcellation of the Human Cerebral Cortex from Intrinsic Functional Connectivity MRI. Cerebral Cortex (New York, N.Y. : 1991), 28(9), 3095–3114. https://doi.org/10.1093/cercor/bhx179
Taylor, P. A., Gohel, S., Di, X., Walter, M., & Biswal, B. B. (2012). Functional covariance networks: Obtaining resting-state networks from intersubject variability. Brain Connectivity, 2(4), 203–217. https://doi.org/10.1089/brain.2012.0095
Tzourio-Mazoyer, N., Landeau, B., Papathanassiou, D., Crivello, F., Etard, O., Delcroix, N., Mazoyer, B., & Joliot, M. (2002). Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single-subject brain. NeuroImage, 15(1), 273–289. https://doi.org/10.1006/nimg.2001.0978
Zang, Y., Jiang, T., Lu, Y., He, Y., & Tian, L. (2004). Regional homogeneity approach to fMRI data analysis. NeuroImage, 22(1), 394–400. https://doi.org/10.1016/j.neuroimage.2003.12.030
No