Changes in brain functional networks in remitted major depressive disorder: a six-month follow-up study

• Published in: BMC psychiatry Vol. 23; no. 1; pp. 1 - 628
• Main Authors: Zhong, Jiaqi, Xu, Jingren, Wang, Zhenzhen, Yang, Hao, Li, Jiawei, Yu, Haoran, Huang, Wenyan, Wan, Cheng, Ma, Hui, Zhang, Ning
• Format: Journal Article
• Language: English
• Published: London BioMed Central Ltd 28.08.2023; BioMed Central; BMC
• Subjects: Analysis; Antidepressants; Brain; Central executive network; Clinical trials; Cognition & reasoning; Complications and side effects; Contraindications; Cortex (parietal); Default mode network; Diagnosis; Drug therapy; Electroconvulsive therapy; Hospitals; Informed consent; Magnetic resonance imaging; Major depressive disorder; Mental depression; Mental disorders; Mental health; Neural networks; Neuroimaging; Prefrontal cortex; Psychiatrists; Psychiatry; Psychosocial functioning; Psychotherapy; Quality of life; Questionnaires; Remission; Remission (Medicine); Remitted major depressive disorder; Salience network; Social interactions; China
• ISSN: 1471-244X; 1471-244X
• DOI: 10.1186/s12888-023-05082-3

Abstract Background Patients with remitted major depressive disorder (rMDD) show abnormal functional connectivity of the central executive network (CEN), salience networks (SN) and default mode network (DMN). It is unclear how these change during remission, or whether changes are related to function. Methods Three spatial networks in 17 patients with rMDD were compared between baseline and the six-month follow-up, and to 22 healthy controls. Correlations between these changes and psychosocial functioning were also assessed. Results In the CEN, patients at baseline had abnormal functional connectivity in the right anterior cingulate, right dorsolateral prefrontal cortex (DLPFC) and inferior parietal lobule (IPL) compare with HCs. There were functional connection differences in the right DLPFC and left IPL at baseline during follow-up. Abnormal connectivity in the right DLPFC and medial prefrontal cortex (mPFC) were found at follow-up. In the SN, patients at baseline had abnormal functional connectivity in the insula, left anterior cingulate, left IPL, and right precuneus; compared with baseline, patients had higher connectivity in the right DLPFC at follow-up. In the DMN, patients at baseline had abnormal functional connectivity in the right mPFC. Resting-state functional connectivity of the IPL and DLPFC in the CEN correlated with psychosocial functioning. Conclusions At six-month follow-up, the CEN still showed abnormal functional connectivity in those with rMDD, while anomalies in the SN and DMN has disappeared. Resting-state functional connectivity of the CEN during early rMDD is associated with psychosocial function. Clinical trials Registration Pharmacotherapy and Psychotherapy for MDD after Remission on Psychology and Neuroimaging. https://www.clinicaltrials.gov/ , registration number: NCT01831440 (15/4/2013).