TY - JOUR
T1 - Altered resting-state functional connectome in major depressive disorder
T2 - a mega-analysis from the PsyMRI consortium
AU - Javaheripour, Nooshin
AU - Li, Meng
AU - Chand, Tara
AU - Krug, Axel
AU - Kircher, Tilo
AU - Dannlowski, Udo
AU - Nenadić, Igor
AU - Hamilton, J. Paul
AU - Sacchet, Matthew D.
AU - Gotlib, Ian H.
AU - Walter, Henrik
AU - Frodl, Thomas
AU - Grimm, Simone
AU - Harrison, Ben J.
AU - Wolf, Christian Robert
AU - Olbrich, Sebastian
AU - van Wingen, Guido
AU - Pezawas, Lukas
AU - Parker, Gordon
AU - Hyett, Matthew P.
AU - Sämann, Philipp G.
AU - Hahn, Tim
AU - Steinsträter, Olaf
AU - Jansen, Andreas
AU - Yuksel, Dilara
AU - Kämpe, Robin
AU - Davey, Christopher G.
AU - Meyer, Bernhard
AU - Bartova, Lucie
AU - Croy, Ilona
AU - Walter, Martin
AU - Wagner, Gerd
PY - 2021/12
Y1 - 2021/12
N2 - Major depressive disorder (MDD) is associated with abnormal neural circuitry. It can be measured by assessing functional connectivity (FC) at resting-state functional MRI, that may help identifying neural markers of MDD and provide further efficient diagnosis and monitor treatment outcomes. The main aim of the present study is to investigate, in an unbiased way, functional alterations in patients with MDD using a large multi-center dataset from the PsyMRI consortium including 1546 participants from 19 centers (www.psymri.com). After applying strict exclusion criteria, the final sample consisted of 606 MDD patients (age: 35.8 ± 11.9 y.o.; females: 60.7%) and 476 healthy participants (age: 33.3 ± 11.0 y.o.; females: 56.7%). We found significant relative hypoconnectivity within somatosensory motor (SMN), salience (SN) networks and between SMN, SN, dorsal attention (DAN), and visual (VN) networks in MDD patients. No significant differences were detected within the default mode (DMN) and frontoparietal networks (FPN). In addition, alterations in network organization were observed in terms of significantly lower network segregation of SMN in MDD patients. Although medicated patients showed significantly lower FC within DMN, FPN, and SN than unmedicated patients, there were no differences between medicated and unmedicated groups in terms of network organization in SMN. We conclude that the network organization of cortical networks, involved in processing of sensory information, might be a more stable neuroimaging marker for MDD than previously assumed alterations in higher-order neural networks like DMN and FPN.
AB - Major depressive disorder (MDD) is associated with abnormal neural circuitry. It can be measured by assessing functional connectivity (FC) at resting-state functional MRI, that may help identifying neural markers of MDD and provide further efficient diagnosis and monitor treatment outcomes. The main aim of the present study is to investigate, in an unbiased way, functional alterations in patients with MDD using a large multi-center dataset from the PsyMRI consortium including 1546 participants from 19 centers (www.psymri.com). After applying strict exclusion criteria, the final sample consisted of 606 MDD patients (age: 35.8 ± 11.9 y.o.; females: 60.7%) and 476 healthy participants (age: 33.3 ± 11.0 y.o.; females: 56.7%). We found significant relative hypoconnectivity within somatosensory motor (SMN), salience (SN) networks and between SMN, SN, dorsal attention (DAN), and visual (VN) networks in MDD patients. No significant differences were detected within the default mode (DMN) and frontoparietal networks (FPN). In addition, alterations in network organization were observed in terms of significantly lower network segregation of SMN in MDD patients. Although medicated patients showed significantly lower FC within DMN, FPN, and SN than unmedicated patients, there were no differences between medicated and unmedicated groups in terms of network organization in SMN. We conclude that the network organization of cortical networks, involved in processing of sensory information, might be a more stable neuroimaging marker for MDD than previously assumed alterations in higher-order neural networks like DMN and FPN.
UR - http://www.scopus.com/inward/record.url?scp=85116567159&partnerID=8YFLogxK
U2 - 10.1038/s41398-021-01619-w
DO - 10.1038/s41398-021-01619-w
M3 - Article
C2 - 34620830
AN - SCOPUS:85116567159
SN - 2158-3188
VL - 11
JO - Translational Psychiatry
JF - Translational Psychiatry
IS - 1
M1 - 511
ER -