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DOI 10.1016/j.pscychresns.2019.04.008

Медицинская библиотека · Psychiatry research. Neuroimaging · 2019

Resting-state functional connectivity in medication-naïve adolescents with major depressive disorder.

Lee Jeonho, Pavuluri Mani N, Kim Ji Hyun, Suh Sangil, Kim Inseong, Lee Moon-Soo

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

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-naïve adolescent MDD patients. Twenty-three drug-naïve adolescents diagnosed with first-episode MDD and 27 healthy participants were enrolled. Seed-to-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-naïve 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.

Для цитирования: Lee Jeonho, Pavuluri Mani N, Kim Ji Hyun, Suh Sangil, Kim Inseong, Lee Moon-Soo. Resting-state functional connectivity in medication-naïve adolescents with major depressive disorder.. Psychiatry research. Neuroimaging. 2019. DOI: 10.1016/j.pscychresns.2019.04.008.

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