Quantitative in vivo evidence for broad regional gradients in the timing of white matter maturation during adolescence

被引:60
|
作者
Colby, John B. [2 ]
Van Horn, John D.
Sowell, Elizabeth R. [1 ,3 ]
机构
[1] Univ Calif Los Angeles, Dept Neurol, David Geffen Sch Med, Dev Cognit Neuroimaging Grp,LONI, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Interdept Program Biomed Engn, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Interdept Program Neurosci, Los Angeles, CA 90095 USA
关键词
White matter; Myelin; Diffusion; DTI; Development; Gradient; COGNITIVE CONTROL; LATE CHILDHOOD; FRACTIONAL ANISOTROPY; CORTICAL DEVELOPMENT; SPATIAL STATISTICS; BRAIN-DEVELOPMENT; YOUNG ADULTHOOD; DIFFUSION; CHILDREN; MRI;
D O I
10.1016/j.neuroimage.2010.08.014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A fundamental tenet in the field of developmental neuroscience is that brain maturation generally proceeds from posterior/inferior to anterior/superior. This pattern is thought to underlie the similar timing of cognitive development in related domains, with the dorsal frontal cortices-important for decision making and cognitive control-the last to fully mature. While this caudal to rostral wave of structural development was first qualitatively described for white matter in classical postmortem studies, and has been discussed frequently in the developmental neuroimaging literature and in the popular press, it has never been formally demonstrated continuously and quantitatively across the whole brain with magnetic resonance imaging (MRI). Here we use diffusion imaging to map developmental changes in the white matter in 32 typically-developing individuals age 5-28 years. We then employ a novel meta-statistic that is sensitive to the timing of this developmental trajectory, and use this integrated strategy to both confirm these long-postulated broad regional gradients in the timing of white matter maturation in vivo, and demonstrate a surprisingly smooth transition in the timing of white matter maturational peaks along a caudal-rostral arc in this cross-sectional sample. These results provide further support for the notion of continued plasticity in these regions well into adulthood, and may provide a new approach for the investigation of neurodevelopmental disorders that could alter the timing of this typical developmental sequence. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:25 / 31
页数:7
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