Comparative analysis of default mode networks in major psychiatric disorders using resting-state EEG

Authors
Choi, Kang-MinKim, Jeong-YounKim, Yong-WookHan, Jung-WonIm, Chang-HwanLee, Seung-Hwan
Issue Date
2021-11
Publisher
Nature Publishing Group
Citation
Scientific Reports, v.11, no.1
Abstract
Default mode network (DMN) is a set of functional brain structures coherently activated when individuals are in resting-state. In this study, we constructed multi-frequency band resting-state EEG-based DMN functional network models for major psychiatric disorders to easily compare their pathophysiological characteristics. Phase-locking values (PLVs) were evaluated to quantify functional connectivity; global and nodal clustering coefficients (CCs) were evaluated to quantify global and local connectivity patterns of DMN nodes, respectively. DMNs of patients with post-traumatic stress disorder (PTSD), obsessive compulsive disorder (OCD), panic disorder, major depressive disorder (MDD), bipolar disorder, schizophrenia (SZ), mild cognitive impairment (MCI), and Alzheimer's disease (AD) were constructed relative to their demographically-matched healthy control groups. Overall DMN patterns were then visualized and compared with each other. In global CCs, SZ and AD showed hyper-clustering in the theta band; OCD, MCI, and AD showed hypo-clustering in the low-alpha band; OCD and MDD showed hypo-clustering and hyper-clustering in low-beta, and high-beta bands, respectively. In local CCs, disease-specific patterns were observed. In the PLVs, lowered theta-band functional connectivity between the left lingual gyrus and the left hippocampus was frequently observed. Our comprehensive comparisons suggest EEG-based DMN as a useful vehicle for understanding altered brain networks of major psychiatric disorders.
Keywords
OBSESSIVE-COMPULSIVE DISORDER; FUNCTIONAL CONNECTIVITY; ALZHEIMERS-DISEASE; BRAIN; MEMORY; PTSD; SCHIZOPHRENIA; HETEROGENEITY; METAANALYSIS; ANATOMY
ISSN
2045-2322
URI
https://pubs.kist.re.kr/handle/201004/116157
DOI
10.1038/s41598-021-00975-3
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KIST Article > 2021
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