Abstract
Premature birth is highly prevalent and associated with neurodevelopmental delays and disorders. Adverse outcomes, particularly in children born before 32 weeks of gestation, have been attributed in large part to white matter injuries, often found in periventricular regions using conventional imaging. To date, tractography studies of white matter pathways in children and adolescents born preterm have evaluated only a limited number of tracts simultaneously. The current study compares diffusion properties along 18 major cerebral white matter pathways in children and adolescents born preterm (n = 27) and full term (n = 19), using diffusion magnetic resonance imaging and tractography. We found that compared to the full term group, the preterm group had significantly decreased FA in segments of the bilateral uncinate fasciculus and anterior segments of the right inferior fronto-occipital fasciculus. Additionally, the preterm group had significantly increased FA in segments of the right and left anterior thalamic radiations, posterior segments of the right inferior fronto-occipital fasciculus, and the right and left inferior longitudinal fasciculus. Increased FA in the preterm group was generally associated with decreased radial diffusivity. These findings indicate that prematurity-related white matter differences in later childhood and adolescence do not affect all tracts in the periventricular zone and can involve both decreased and increased FA. Differences in the patterns of radial diffusivity and axial diffusivity suggest that the tissue properties underlying group FA differences may vary within and across white matter tracts. Distinctive diffusion properties may relate to variations in the timing of injury in the neonatal period, extent of white matter dysmaturity and/or compensatory processes in childhood.
Original language | English |
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Article number | e0142860 |
Journal | PLoS ONE |
Volume | 10 |
Issue number | 11 |
DOIs | |
State | Published - 1 Nov 2015 |
Bibliographical note
Publisher Copyright:© 2015 Travis et al.This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding
This work has been supported by the National Institutes of Health, NICHD grants (RO1-HD69162, RO1-HD46500). These grants were awarded to HMF and used to support data collection, salary support for KETand JNA, and collaboration with MBS. The Clinical and Translational Science Award 1UL1 RR025744 for the Stanford Center for Clinical and Translational Education and Research (Spectrum) from the National Center for Research Resources, National Institutes of Health provided institutional support. Grant support to MBS came from the I-CORE Program of the Planning and Budgeting Committee and The Israel Science Foundation, Grants No. 51/11 and 513/11. We thank the children and families who participated in our study; V Kovachy and I Loe for helpful suggestions regarding the analyses; and the developmental-behavioral pediatrics research group for discussions of the results.
Funders | Funder number |
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National Institutes of Health | |
National Institute of Child Health and Human Development | R01HD046500 |
National Center for Research Resources | |
Spectrum Pharmaceuticals | |
Eunice Kennedy Shriver National Institute of Child Health and Human Development | RO1-HD69162, 1UL1 RR025744 |
Center for Clinical and Translational Research | |
Israel Science Foundation | 51/11, 513/11 |
Israeli Centers for Research Excellence |