An intracellular isotropic diffusion signal is positively associated with pubertal development in white matter

被引:1
作者
Newman, Benjamin T. [1 ,3 ]
Patrie, James T. [2 ]
Druzgal, T. Jason [1 ]
机构
[1] Univ Virginia, Sch Med, Dept Radiol & Med Imaging, Charlottesville, VA USA
[2] Univ Virginia, Sch Med, Dept Publ Hlth Sci, Charlottesville, VA USA
[3] MR4 409 Lane Rd, Charlottesville, VA 22903 USA
关键词
Diffusion; Microstructure; MRI; Development; Puberty; HUMAN BRAIN; ADOLESCENT BRAIN; FIBER DENSITY; IN-VIVO; TESTOSTERONE; TISSUE; PREVALENCE; DISORDERS; CHILDHOOD; MOVEMENT;
D O I
10.1016/j.dcn.2023.101301
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Puberty is a key event in adolescent development that involves significant, hormone-driven changes to many aspects of physiology including the brain. Understanding how the brain responds during this time period is important for evaluating neuronal developments that affect mental health throughout adolescence and the adult lifespan. This study examines diffusion MRI scans from the cross-sectional ABCD Study baseline cohort, a large multi-site study containing thousands of participants, to describe the relationship between pubertal development and brain microstructure. Using advanced, 3-tissue constrained spherical deconvolution methods, this study is able to describe multiple tissue compartments beyond only white matter (WM) axonal qualities. After controlling for age, sex, brain volume, subject handedness, scanning site, and sibling relationships, we observe a positive relationship between an isotropic, intracellular diffusion signal fraction and pubertal development across a majority of regions of interest (ROIs) in the WM skeleton. We also observe regional effects from an intracellular anisotropic signal fraction compartment and extracellular isotropic free water-like compartment in several ROIs. This cross-sectional work suggests that changes in pubertal status are associated with a complex response from brain tissue that cannot be completely described by traditional methods focusing only on WM axonal properties.
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页数:12
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