Frontoparietal function in young people with dysthymic disorder (DSM-5: Persistent depressive disorder) during
Veronika Vilgis1, Jian Chen2, Timothy J Silk2
1Developmental Imaging, Murdoch Childrens Research Institute, Parkville, VIC, Australia; Academic Child Psychiatry Unit, Department of Paediatrics, University of Melbourne, Royal Children׳s Hospital, Parkville, Melbourne 3062, VIC, Australia.
Young people with dysthymic disorder (DD) show altered brain activity in frontal regions during working memory tasks. These findings suggest a continuity in the pathophysiology of depressive disorders across the lifespan.
Area of Science:
- Neuroscience
- Developmental Psychology
- Psychiatry
Background:
- Dysthymic disorder (DD) is a persistent mood disorder and a risk factor for major depressive disorder (MDD).
- Both DD and MDD are linked to executive function deficits, particularly in working memory and attention.
- Brain network alterations in youth with DD are poorly understood.
Purpose of the Study:
- To investigate brain function associated with spatial working memory in children and adolescents with DD.
- To compare brain activity in DD patients with age-, gender-, and IQ-matched typically developing controls using fMRI.
Main Methods:
- Nineteen medication-naïve male patients with DD and 16 typically developing boys underwent fMRI.
- Participants completed two spatial working memory tasks: mental rotation and delay-match to sample (DMTS).
Main Results:
- The DD group exhibited reduced activation in left prefrontal cortex (PFC) regions during mental rotation compared to controls.
- Reduced activation was also observed in medial frontal regions, including the dorsomedial PFC, anterior cingulate cortex, and frontal pole.
- During the DMTS task, patients showed increased activation in the right precuneus and posterior cingulate cortex.
Conclusions:
- Findings in youth with DD complement adult MDD studies, highlighting altered left PFC function during working memory.
- Altered function of cortical midline structures was identified in young DD patients.
- Results suggest the pathophysiology of depressive disorders extends to DD, showing continuity across the lifespan.
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