4.6 Article

Evaluating the Prediction of Brain Maturity From Functional Connectivity After Motion Artifact Denoising

Journal

CEREBRAL CORTEX
Volume 29, Issue 6, Pages 2455-2469

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cercor/bhy117

Keywords

development; fMRI; functional connectivity; machine learning

Categories

Funding

  1. NIH [R01NS046424, K01MH104592, K23NS088590, R01HD057076, R21MH091512, R21 NS091635, K23DC006638, P50 MH071616, P60 DK020579-31]
  2. NARSAD Young Investigator Award
  3. NIH NINDS [NRSA-F32 NS656492, F32NS092290]
  4. Simons Foundation Autism Research Initiative
  5. Tourette Association of America Neuroimaging Consortium Grant
  6. American Hearing Research Foundation
  7. McDonnell Foundation
  8. Eunice Kennedy Shriver National Institute Of Child Health & Human Development of the National Institutes of Health [U54 HD087011]

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The ability to make individual-level predictions from neuroanatomy has the potential to be particularly useful in child development. Previously, resting-state functional connectivity (RSFC) MRI has been used to successfully predict maturity and diagnosis of typically and atypically developing individuals. Unfortunately, submillimeter head motion in the scanner produces systematic, distance-dependent differences in RSFC and may contaminate, and potentially facilitate, these predictions. Here, we evaluated individual age prediction with RSFC after stringent motion denoising. Using multivariate machine learning, we found that 57% of the variance in individual RSFC after motion artifact denoising was explained by age, while 4% was explained by residual effects of head motion. When RSFC data were not adequately denoised, 50% of the variance was explained by motion. Reducing motion-related artifact also revealed that prediction did not depend upon characteristics of functional connections previously hypothesized to mediate development (e.g., connection distance). Instead, successful age prediction relied upon sampling functional connections across multiple functional systems with strong, reliable RSFC within an individual. Our results demonstrate that RSFC across the brain is sufficiently robust to make individual-level predictions of maturity in typical development, and hence, may have clinical utility for the diagnosis and prognosis of individuals with atypical developmental trajectories.

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