TY - JOUR
T1 - Altered White-matter Tract Property in Adults with Attention-deficit Hyperactivity Disorder
AU - Chiang, Huey Ling
AU - Yang, Li Kuang
AU - Chen, Yu Jen
AU - Hsu, Yung Chin
AU - Lo, Yu Chun
AU - Tseng, Wen Yih Isaac
AU - Gau, Susan Shur Fen
N1 - Funding Information:
All the authors report no financial relationships with commercial interests. This work was supported by the Ministry of Science and Technology, Taiwan ( MOST103-2314-B-002-021-MY3 ), Chen-Yung Foundation , and National Health Research Institute, Taiwan ( NHRI-EX101-10008PI NHRI-EX102-10008PI NHRI-EX103-10008PI ).
Publisher Copyright:
© 2022 IBRO
PY - 2022/4/1
Y1 - 2022/4/1
N2 - Although altered microstructure properties of white-matter tracts have been reported in children with attention-deficit/hyperactivity disorder (ADHD), findings from relatively few adult ADHD studies are inconsistent. This study aims to examine microstructural property over the whole brain in adults with ADHD and explore structural connectivities. Sixty-four medication-naïve adults with ADHD and 81 healthy adults received diffusion spectrum imaging. Generalized fractional anisotropy (GFA), an index indicating microstructural property, was calculated stepwise among 76 white-matter tracts. With the threshold-free clustering weighted method, the segments with the largest group difference were selected, and mean GFA (mGFA) values were calculated. Adults with ADHD had increased mGFA values in the segments located in the left frontal aslant tract, the right inferior longitudinal fasciculus, and the left perpendicular fasciculus, and reduced mGFA values in the segments located in the right superior longitudinal fasciculus (SLF) I, the left SLF II, the right frontostriatal tracts from dorsolateral prefrontal cortex and the ventrolateral prefrontal cortex, the right medial lemniscus, the right inferior thalamic radiation to the auditory cortex, and the callosal fibers. Additionally, the mGFA value of the right SLF I segment was associated with hyperactivity-impulsivity symptoms. Our findings suggest that white-matter tracts with altered microstructure properties are located within the attention networks, fronto-striato-thalamocortical regions, and those associated with attention and visual perception in adults with ADHD.
AB - Although altered microstructure properties of white-matter tracts have been reported in children with attention-deficit/hyperactivity disorder (ADHD), findings from relatively few adult ADHD studies are inconsistent. This study aims to examine microstructural property over the whole brain in adults with ADHD and explore structural connectivities. Sixty-four medication-naïve adults with ADHD and 81 healthy adults received diffusion spectrum imaging. Generalized fractional anisotropy (GFA), an index indicating microstructural property, was calculated stepwise among 76 white-matter tracts. With the threshold-free clustering weighted method, the segments with the largest group difference were selected, and mean GFA (mGFA) values were calculated. Adults with ADHD had increased mGFA values in the segments located in the left frontal aslant tract, the right inferior longitudinal fasciculus, and the left perpendicular fasciculus, and reduced mGFA values in the segments located in the right superior longitudinal fasciculus (SLF) I, the left SLF II, the right frontostriatal tracts from dorsolateral prefrontal cortex and the ventrolateral prefrontal cortex, the right medial lemniscus, the right inferior thalamic radiation to the auditory cortex, and the callosal fibers. Additionally, the mGFA value of the right SLF I segment was associated with hyperactivity-impulsivity symptoms. Our findings suggest that white-matter tracts with altered microstructure properties are located within the attention networks, fronto-striato-thalamocortical regions, and those associated with attention and visual perception in adults with ADHD.
KW - ADHD
KW - adult
KW - diffusion spectrum imaging
KW - hyperactivity-impulsivity
KW - tract-specific analysis
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U2 - 10.1016/j.neuroscience.2022.01.027
DO - 10.1016/j.neuroscience.2022.01.027
M3 - Article
C2 - 35131395
AN - SCOPUS:85125856236
SN - 0306-4522
VL - 487
SP - 78
EP - 87
JO - Neuroscience
JF - Neuroscience
ER -