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Authors Xia W, Zhou R, Zhao G, Wang F, Mao R, Peng D, Yang T, Wang Z, Chen J, Fang Y
Received 29 March 2018
Accepted for publication 21 May 2018
Published 10 August 2018 Volume 2018:14 Pages 2017—2026
DOI https://doi.org/10.2147/NDT.S169583
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Andrew Yee
Peer reviewer comments 2
Editor who approved publication: Professor Wai Kwong Tang
Background: Almost half of patients with major depressive disorder (MDD) also
have clinically meaningful levels of anxiety. Anxious depression is a distinct
clinical subtype of MDD, which has poor response to pharmacotherapy; however,
the neural mechanisms behind are largely unknown. In the present study, we
explored the white matter (WM) integrity traits of anxious depression in
first-episode and medication-free (medication-naïve and medication washout)
Chinese young adult patients by detecting differences in diffusion tensor
imaging (DTI) with the tract-based spatial statistics (TBSS) method.
Subjects and methods: DTI was obtained from 39 first-episode,
medication-free anxious depressive patients, 45 nonanxious depressive patients,
and 50 demographically similar healthy controls. All subjects underwent
clinical assessments. TBSS was carried out to investigate the difference in WM
integrity among three groups within DTI parameter maps. WM integrity was
measured using fractional anisotropy (FA), mean diffusivity, axial diffusivity,
and radial diffusivity (RD). The correlations between WM integrity and clinical
features were also computed.
Results: When compared with nonanxious patients, lower FA
values in anxious depressive patients were found in multiple regions of the
brain, mainly involving left uncinate fasciculus (UF), superior longitudinal
fasciculus (SLF), and forceps major and minor. Higher RD in forceps major and minor
and SLF were also detected. The decreased FA values and increased RD values
correlated with both anxiety level and depression level in the pooled
depressive group.
Conclusion: The anxious depressive patients had more
abnormalities in WM integrity at the early phase than the nonanxious group.
Alternations in WM integrity in fiber pathways, including SLF, UF, and forceps
major and minor, may play a critical role in the neuropathology of anxious
depression and might help to identify anxious MDD from nonanxious MDD. Further
study with larger sample size, larger age range, and longitudinal design is
needed to confer a robust inference to better understand the dynamic
neurological change and neuropathology of WM integrity in anxious MDD.
Keywords: diffusion tensor
imaging, anxious depression, tract-based spatial statistics, micro-structure of
whiter matter