TY - JOUR
T1 - Altered electroencephalography resting state network coherence in remitted MDD
AU - Ray, Kimberly L.
AU - Griffin, Nicholas R.
AU - Shumake, Jason
AU - Alario, Alexandra
AU - Allen, John J.B.
AU - Beevers, Christopher G.
AU - Schnyer, David M.
N1 - Funding Information: We would like to thank the participants who gave generously of their time. This work was supported by the National Institutes of Health [NIMH R56MH108650]. Data have been made available on the Texas Data Repository (https://doi.org/10.18738/T8/ASIX6C). Publisher Copyright: © 2023
PY - 2023/5/1
Y1 - 2023/5/1
N2 - Individuals with remitted depression are at greater risk for subsequent depression and therefore may provide a unique opportunity to understand the neurophysiological correlates underlying the risk of depression. Research has identified abnormal resting-state electroencephalography (EEG) power metrics and functional connectivity patterns associated with major depression, however little is known about these neural signatures in individuals with remitted depression. We investigate the spectral dynamics of 64-channel EEG surface power and source-estimated network connectivity during resting states in 37 individuals with depression, 56 with remitted depression, and 49 healthy adults that did not differ on age, education, and cognitive ability across theta, alpha, and beta frequencies. Average reference spectral EEG surface power analyses identified greater left and midfrontal theta in remitted depression compared to healthy adults. Using Network Based Statistics, we also demonstrate within and between network alterations in LORETA transformed EEG source-space coherence across the default mode, fronto-parietal, and salience networks where individuals with remitted depression exhibited enhanced coherence compared to those with depression, and healthy adults. This work builds upon our currently limited understanding of resting EEG connectivity in depression, and helps bridge the gap between aberrant EEG power and brain network connectivity dynamics in this disorder. Further, our unique examination of remitted depression relative to both healthy and depressed adults may be key to identifying brain-based biomarkers for those at high risk for future, or subsequent depression.
AB - Individuals with remitted depression are at greater risk for subsequent depression and therefore may provide a unique opportunity to understand the neurophysiological correlates underlying the risk of depression. Research has identified abnormal resting-state electroencephalography (EEG) power metrics and functional connectivity patterns associated with major depression, however little is known about these neural signatures in individuals with remitted depression. We investigate the spectral dynamics of 64-channel EEG surface power and source-estimated network connectivity during resting states in 37 individuals with depression, 56 with remitted depression, and 49 healthy adults that did not differ on age, education, and cognitive ability across theta, alpha, and beta frequencies. Average reference spectral EEG surface power analyses identified greater left and midfrontal theta in remitted depression compared to healthy adults. Using Network Based Statistics, we also demonstrate within and between network alterations in LORETA transformed EEG source-space coherence across the default mode, fronto-parietal, and salience networks where individuals with remitted depression exhibited enhanced coherence compared to those with depression, and healthy adults. This work builds upon our currently limited understanding of resting EEG connectivity in depression, and helps bridge the gap between aberrant EEG power and brain network connectivity dynamics in this disorder. Further, our unique examination of remitted depression relative to both healthy and depressed adults may be key to identifying brain-based biomarkers for those at high risk for future, or subsequent depression.
KW - Coherence
KW - Connectivity
KW - Depression
KW - EEG
KW - MDD
KW - Resting state
UR - http://www.scopus.com/inward/record.url?scp=85148770455&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85148770455&partnerID=8YFLogxK
U2 - 10.1016/j.brainres.2023.148282
DO - 10.1016/j.brainres.2023.148282
M3 - Article
C2 - 36792002
SN - 0006-8993
VL - 1806
JO - Brain Research
JF - Brain Research
M1 - 148282
ER -