Subcortical Neural Synchronization predicts biological Mother-Child relationship

Poster No:

1889 

Submission Type:

Abstract Submission 

Authors:

Jihyun Bae1, Yong Jeon Cheong1, Seonkyoung Lee1, Jihyeong Ro2, Minyoung Jung1

Institutions:

1Korea Brain Research Institute, Daegu, Korea, Republic of, 2Kyungpook National University, Daegu, Korea, Republic of

First Author:

Jihyun Bae  
Korea Brain Research Institute
Daegu, Korea, Republic of

Co-Author(s):

Yong Jeon Cheong  
Korea Brain Research Institute
Daegu, Korea, Republic of
Seonkyoung Lee  
Korea Brain Research Institute
Daegu, Korea, Republic of
Jihyeong Ro  
Kyungpook National University
Daegu, Korea, Republic of
Minyoung Jung  
Korea Brain Research Institute
Daegu, Korea, Republic of

Introduction:

Interpersonal neural synchronization (INS) has been considered as an indicator of relationship closeness and cooperative interactions. [1-2] Considering that mother-child is the closest social relation, it raises a series of questions: does a mother exhibit greater INS with her own child compared to other child? If so, are there any key brain regions or neural networks characterizing biological relationships? Exploring INS across brain regions and large-scale functional networks, this study aims to address these questions.

Methods:

This study included 122 biological mother-child pairs (mean age [SD] = 40.87 [2.91] years for mothers; 68 boys, mean age [SD] = 9.3 [1.63] years for children). Resting-state functional magnetic resonance imaging (rs-fMRI) and T1-weighted imaging were performed using a 3T scanner. Neuroimaging data were preprocessed using the CONN toolbox. We assessed INS of 90 parcellated regions of interest (ROIs) based on phase values [3] using the Funpsy toolbox implemented in MATLAB. [4-5] We computed phase locking values (PLVs) of the corresponding ROIs across biological and non-biological mothers and children within the Automated Anatomical Labeling (AAL) atlas, excluding the cerebellum. A linear mixed effects model (LMEM) was applied to predict biological pairs from pairwise PLVs, controlling for age and gender. [6] We are currently investigating how INS of large-scale brain networks predict biological relationships. We explored eight networks, seven canonical functional networks defined by Yeo et al. [7] and an additional one comprising 10 ROIs that we identified in regions-wise analysis.
Supporting Image: 2025OHBMfigure_resized.png
   ·Overview of processing
 

Results:

Significant INSs to predict biological relationships were found in the bilateral olfactory gyrus (p=1.9E-06 (β=-0.0069) for left;, p=1.5E-04 (β=-0.0059) right hemispheres , bilateral thalamus (p=8.4E-05 (β=-0.006) for left;, p=1.67E-3 (β=-0.0053) for right), bilateral putamen (p=1.5E-04 (β=-0.006) for left ; p=3.3E-04 (β=-0.006) for right), left amygdala (p=0.0007, β=-0.0055), right heschl gyrus (p=0.0068, β=-0.0049), and left parahippocampal gyrus (p=0.0082, β=-0.0048).

Conclusions:

Biological mother and child relationship is characterized by significantly higher neural synchronization, compared to non-biological pairs. It is interesting that the bilateral olfactory gyrus is the key brain regions for prediction of biological kinship. This is in line with the reporting significant role of the olfactory gyrus in maternal bonding via the processing of olfactory information and emotional cues. [8-9] Regarding our findings of significance of INS of limbic system including the basal ganglia in biological relationship, the systems are known for its role in emotional attunement. [10] Compared to previous INS studies using goal directed tasks (i.e., joint action, video watching, etc.), our study used rs-fMRI. It implies not only that biological kinship may differ from other social relationships but also that tasks may not be mandatory for prediction of close relationships.

Emotion, Motivation and Social Neuroscience:

Social Neuroscience Other

Modeling and Analysis Methods:

fMRI Connectivity and Network Modeling 2
Multivariate Approaches

Novel Imaging Acquisition Methods:

BOLD fMRI 1

Physiology, Metabolism and Neurotransmission:

Neurophysiology of Imaging Signals

Keywords:

Computational Neuroscience
Congenital
Data analysis
FUNCTIONAL MRI
Limbic Systems
MRI
NORMAL HUMAN
Statistical Methods
Other - Linear mixed effects model (LMEM), phase locking value (PLV)

1|2Indicates the priority used for review

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Provide references using APA citation style.

1. Parkinson, C., Kleinbaum, A. M., & Wheatley, T. (2018). Similar neural responses predict friendship. Nature Communications, 9(1), 332. https://doi.org/10.1038/s41467-017-02722-7
2. Li, L., Liu, J., Zhang, Y., & Huang, Y. (2022). Neural synchronization predicts marital satisfaction. Proceedings of the National Academy of Sciences of the United States of America, 119(38), e2207150119. https://doi.org/10.1073/pnas.2207150119
3. Zhao, Q., Gao, Y., Zhang, Z., Liu, J., & He, C. (2024). Interpersonal neural synchronization during social interactions in close relationships: A systematic review and meta-analysis of fNIRS hyperscanning studies. Neuroscience & Biobehavioral Reviews, 158, 105659. https://doi.org/10.1016/j.neubiorev.2024.105659
4. Aydore, S., Pantazis, D., & Leahy, R. M. (2013). A note on the phase locking value and its properties. NeuroImage, 74, 231–244. https://doi.org/10.1016/j.neuroimage.2013.02.041
5. Honari, H., Hashemi, R., & Aghajani, H. (2021). Evaluating phase synchronization methods in fMRI: A comparison study and new approaches. NeuroImage, 224, 117406. https://doi.org/10.1016/j.neuroimage.2020.117406
6. Enrico, G., Bianchi, A. M., & Cerutti, S. (2012). Functional magnetic resonance imaging phase synchronization as a measure of dynamic functional connectivity. Brain Connectivity, 2(5), 275–288. https://doi.org/10.1089/brain.2012.0082
7. Chen, G., Saad, Z. S., Britton, J. C., Pine, D. S., & Cox, R. W. (2013). Linear mixed-effects modeling approach to fMRI group analysis. NeuroImage, 73, 176–190. https://doi.org/10.1016/j.neuroimage.2013.01.047
8. Yeo, B. T., Krienen, F. M., Sepulcre, J., Sabuncu, M. R., Lashkari, D., Hollinshead, M., … Buckner, R. L. (2011). The organization of the human cerebral cortex estimated by intrinsic functional connectivity. Journal of Neurophysiology, 106(3), 1125–1165. https://doi.org/10.1152/jn.00338.2011
9. Lévy, F., & Keller, M. (2009). Olfactory mediation of maternal behavior in selected mammalian species. Behavioural Brain Research, 200(2), 336–345. https://doi.org/10.1016/j.bbr.2008.12.017
10. Fuentes, I., Schanzer, A., & Hyman, S. (2022). Experience-regulated neuronal signaling in maternal behavior. Frontiers in Molecular Neuroscience, 15, 837011. https://doi.org/10.3389/fnmol.2022.837011
11. Hikosaka, O., Sesack, S. R., Lecourtier, L., & Shepard, P. D. (2008). Habenula: Crossroad between the basal ganglia and the limbic system. The Journal of Neuroscience, 28(46), 11825–11829.

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