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Updated: May 29, 2026

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Measuring Connectivity in the Primary Visual Pathway in Human Albinism Using Diffusion Tensor Imaging and Tractography
Published on: August 11, 2016
Differential development of human brain white matter tracts
Davide Imperati1, Stan Colcombe, Clare Kelly
1Phyllis Green and Randolph Cowen Institute for Pediatric Neuroscience, Child Study Center, Langone Medical Center, New York University, New York City, New York, United States of America.
Plos One
|September 13, 2011
Summary
This study introduces a new data-driven method to analyze white matter tract development using diffusion tensor imaging. It reveals inverted U-shaped age trajectories for fractional anisotropy, peaking in adulthood and declining thereafter.
Area of Science:
- Neuroscience
- Developmental Neuroscience
- Neuroimaging
Background:
- Human structural and functional connectivity development is a key focus in neuroscience.
- Diffusion-based imaging and tractography show promise but have had limited impact on developmental studies.
- Existing diffusion tensor imaging (DTI) datasets offer potential for novel analytical approaches.
Purpose of the Study:
- To develop and apply a novel data-driven approach to analyze developmental trajectories of white matter tracts.
- To identify similarities and differences in the developmental patterns of various white matter tracts.
- To investigate age-related changes in white matter microstructure using fractional anisotropy (FA).
Main Methods:
- Utilized 64-direction diffusion tensor imaging (DTI) data from 144 healthy individuals aged 7 to 48 years.
- Applied k-means cluster analysis to white matter voxels based on age-related fractional anisotropy (FA) trajectories.
- Identified optimal cluster solutions at 5, 9, and 14 clusters to delineate distinct white matter tracts and subdivisions.
Main Results:
- Successfully recapitulated well-established white matter tracts (e.g., corpus callosum, internal capsule) and their subdivisions.
- Demonstrated curvilinear (inverted 'U-shaped') age-related trajectories for FA in most identified tracts.
- Indicated that FA decreases begin as early as age 23, with a mean onset around age 30, suggesting early age-related microstructural decline.
Conclusions:
- Data-driven analytical techniques can be effectively applied to existing DTI datasets for developmental studies.
- The findings provide new insights into the normative developmental trajectories of white matter integrity across the lifespan.
- This approach holds potential for application in both normative and neuropsychiatric research using DTI data.

