Resting-state functional connectivity in medication-naive adolescents with major depressive disorder
- Authors
- Lee, Jeonho; Pavuluri, Mani N.; Kim, Ji Hyun; Suh, Sangil; Kim, Inseong; Lee, Moon-Soo
- Issue Date
- 30-6월-2019
- Publisher
- ELSEVIER IRELAND LTD
- Keywords
- Depression; First-onset; Conn; Seed-to-voxel; Amygdala; Insula; Hippocampus
- Citation
- PSYCHIATRY RESEARCH-NEUROIMAGING, v.288, pp.37 - 43
- Indexed
- SCIE
SCOPUS
- Journal Title
- PSYCHIATRY RESEARCH-NEUROIMAGING
- Volume
- 288
- Start Page
- 37
- End Page
- 43
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/64716
- DOI
- 10.1016/j.pscychresns.2019.04.008
- ISSN
- 0925-4927
- Abstract
- Adolescence is a vulnerable period for major depressive disorder (MDD). The aim of our study was to investigate resting-state functional connectivity (RSFC) in first-episode, medication-naive adolescent MDD patients. Twenty-three drug-naive adolescents diagnosed with first-episode MDD and 27 healthy participants were enrolled. Seedto-voxel RSFC analyses were performed. The frontolimbic circuit regions of interest included the amygdala, anterior cingulate cortex, insula, and hippocampus. A correlation analysis between the RSFC and Children's Depression Inventory, Hamilton depression rating scale, and duration of episodes was performed. The adolescents with MDD exhibited the following characteristics: a lower RSFC between the right amygdala and right superior frontal gyrus; a lower RSFC between the right hippocampus and clusters including the right insula and right middle frontal gyrus; a higher RSFC between the left insula and clusters including the bilateral middle frontal gyrus, right superior frontal gyrus, and right frontal pole; and a higher RSFC between the left dorsal anterior cingulate cortex and a cluster including the left insula. Medication-naive adolescents with depression display lower connectivity of several brain regions implicated in processing, regulation, and memory of emotions. Higher connectivity was observed in brain regions that potentially explain rumination, impaired concentration, and physiological arousal.
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Collections - College of Medicine > Department of Medical Science > 1. Journal Articles
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