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Resting-state functional connectivity identifies individuals and predicts age in 8-to-26-month-olds.
Kardan, Omid; Kaplan, Sydney; Wheelock, Muriah D; Feczko, Eric; Day, Trevor K M; Miranda-Domínguez, Óscar; Meyer, Dominique; Eggebrecht, Adam T; Moore, Lucille A; Sung, Sooyeon; Chamberlain, Taylor A; Earl, Eric; Snider, Kathy; Graham, Alice; Berman, Marc G; Ugurbil, Kamil; Yacoub, Essa; Elison, Jed T; Smyser, Christopher D; Fair, Damien A; Rosenberg, Monica D.
Affiliation
  • Kardan O; University of Chicago, USA. Electronic address: okardan@uchicago.edu.
  • Kaplan S; Washington University in St. Louis School of Medicine, USA.
  • Wheelock MD; Washington University in St. Louis School of Medicine, USA.
  • Feczko E; University of Minnesota, USA.
  • Day TKM; University of Minnesota, USA.
  • Miranda-Domínguez Ó; University of Minnesota, USA.
  • Meyer D; Washington University in St. Louis School of Medicine, USA.
  • Eggebrecht AT; Washington University in St. Louis School of Medicine, USA.
  • Moore LA; Oregon Health & Science University, USA.
  • Sung S; University of Minnesota, USA.
  • Chamberlain TA; University of Chicago, USA.
  • Earl E; Oregon Health & Science University, USA.
  • Snider K; Oregon Health & Science University, USA.
  • Graham A; Oregon Health & Science University, USA.
  • Berman MG; University of Chicago, USA.
  • Ugurbil K; University of Minnesota, USA.
  • Yacoub E; University of Minnesota, USA.
  • Elison JT; University of Minnesota, USA.
  • Smyser CD; Washington University in St. Louis School of Medicine, USA.
  • Fair DA; University of Minnesota, USA.
  • Rosenberg MD; University of Chicago, USA. Electronic address: mdrosenberg@uchicago.edu.
Dev Cogn Neurosci ; 56: 101123, 2022 08.
Article in En | MEDLINE | ID: mdl-35751994
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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Connectome Type of study: Prognostic_studies / Risk_factors_studies Limits: Adult / Child, preschool / Humans / Infant Language: En Journal: Dev Cogn Neurosci Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Connectome Type of study: Prognostic_studies / Risk_factors_studies Limits: Adult / Child, preschool / Humans / Infant Language: En Journal: Dev Cogn Neurosci Year: 2022 Document type: Article