Resting-state functional connectivity identifies individuals and predicts age in 8-to-26-month-olds
Omid Kardan1, Sydney Kaplan2, Muriah D Wheelock2
1University of Chicago, USA.
Insights
Resting-state functional connectivity (rsFC) in infants and toddlers shows medium reliability and can predict age with reasonable accuracy. Within-network connections are key predictors of brain maturation in early development.
Area of Science:
- Neuroscience
- Developmental Neuroscience
- Neuroimaging
Background:
- Resting-state functional connectivity (rsFC) using fMRI is valuable for studying brain maturation in children and adults.
- Its reliability and predictive power in infants and toddlers remain less understood.
Purpose of the Study:
- To assess the reliability and uniqueness of rsFC in infants and toddlers.
- To predict age using rsFC in this demographic.
- To identify brain networks crucial for age prediction.
Main Methods:
- Utilized fMRI data from the Baby Connectome Project (n=170, ages 8-26 months).
- Measured rsFC reliability and performed functional connectome fingerprinting.
- Employed support vector regression models for age prediction.
- Defined 11 infant-specific functional networks.
Main Results:
- Demonstrated medium within-session rsFC reliability.
- Achieved successful functional connectome fingerprinting.
- Predicted infant age with a ±3.6 month error (R² = .51).
- Found within-network connections were stronger predictors of age than between-network connections.
Conclusions:
- rsFC is a reliable and unique marker for brain development in infants and toddlers.
- Within-network connectivity is vital for predicting age in early development.
- Findings support using rsFC to track functional brain organization and predict developmental outcomes.
Abstract:
Resting-state functional connectivity (rsFC) measured with fMRI has been used to characterize functional brain maturation in typically and atypically developing children and adults. However, its reliability and utility for predicting development in infants and toddlers is less well understood. Here, we use fMRI data from the Baby Connectome Project study to measure the reliability and uniqueness of rsFC in infants and toddlers and predict age in this sample (8-to-26 months old; n = 170). We observed medium reliability for within-session infant rsFC in our sample, and found that individual infant and toddler's connectomes were sufficiently distinct for successful functional connectome fingerprinting. Next, we trained and tested support vector regression models to predict age-at-scan with rsFC. Models successfully predicted novel infants' age within ± 3.6 months error and a prediction R2 = .51. To characterize the anatomy of predictive networks, we grouped connections into 11 infant-specific resting-state functional networks defined in a data-driven manner. We found that connections between regions of the same network-i.e. within-network connections-predicted age significantly better than between-network connections. Looking ahead, these findings can help characterize changes in functional brain organization in infancy and toddlerhood and inform work predicting developmental outcome measures in this age range.
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