Development of frontoparietal connectivity predicts longitudinal symptom changes in young people with autism spectrum disorder

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作者
Hsiang-Yuan Lin
Alistair Perry
Luca Cocchi
James A. Roberts
Wen-Yih Isaac Tseng
Michael Breakspear
Susan Shur-Fen Gau
机构
[1] National Taiwan University Hospital,Department of Psychiatry
[2] and College of Medicine,Systems Neuroscience Group
[3] QIMR Berghofer Medical Research Institute,Center for Lifespan Psychology
[4] Max Planck UCL Centre for Computational Psychiatry and Ageing Research,Clinical Brain Network Team
[5] Max Planck Institute for Human Development,Brain Modeling Team
[6] Max Planck Institute for Human Development,Institute of Medical Device and Imaging
[7] QIMR Berghofer Medical Research Institute,Graduate Institute of Brain and Mind Sciences
[8] QIMR Berghofer Medical Research Institute,Metro North Mental Health Service
[9] National Taiwan University College of Medicine,undefined
[10] National Taiwan University College of Medicine,undefined
[11] The Royal Brisbane and Woman’s Hospital,undefined
[12] University of Newcastle,undefined
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Structural neuroimaging studies suggest altered brain maturation in autism spectrum disorder (ASD) compared with typically developing controls (TDC). However, the prognostic value of whole-brain structural connectivity analysis in ASD has not been established. Diffusion magnetic imaging data were acquired in 27 high-functioning young ASD participants (2 females) and 29 age-matched TDC (12 females; age 8–18 years) at baseline and again following 3–7 years. Whole-brain structural connectomes were reconstructed from these data and analyzed using a longitudinal statistical model. We identified distinct patterns of widespread brain connections that exhibited either significant increases or decreases in connectivity over time (p < 0.001). There was a significant interaction between diagnosis and time in brain development (p < 0.001). This was expressed by a decrease in structural connectivity within the frontoparietal network—and its broader connectivity—in ASD during adolescence and early adulthood. Conversely, these connections increased with time in TDC. Crucially, stronger baseline connectivity in this subnetwork predicted a lower symptom load at follow-up (p = 0.048), independent of the expression of symptoms at baseline. Our findings suggest a clinically meaningful relationship between the atypical development of frontoparietal structural connections and the dynamics of the autism phenotype through early adulthood. These results highlight a potential marker of future outcome.
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