Literature DB >> 32118262

Prefrontal Cortical Reactivity and Connectivity Markers Distinguish Youth Depression from Healthy Youth.

Prabhjot Dhami1,2, Sravya Atluri1,3, Jonathan C Lee1,2,4, Yuliya Knyahnytska1,4, Paul E Croarkin5, Daniel M Blumberger1,2,4, Zafiris J Daskalakis1,2,4, Faranak Farzan1,2,4,6.   

Abstract

Up to 50% of youth with depression do not respond to conventional first-line treatments. However, little research has been conducted on the pathophysiology of youth depression, hindering the identification of more effective treatments. Our goal was to identify neurophysiological markers that differentiate youth with depression from healthy youth and could serve as targets of novel treatments. We hypothesized that youth with depression would exhibit network-specific cortical reactivity and connectivity abnormalities compared with healthy youth. Transcranial magnetic stimulation combined with electroencephalography and magnetic resonance imaging was employed in combination with clinical and behavioral assessments to study cortical reactivity and connectivity in bilateral dorsolateral prefrontal cortex (DLPFC), motor cortex, and inferior parietal lobule, sites linked to the frontoparietal network, sensorimotor network, and default mode network, respectively. In youth depression, greater cortical reactivity was observed specific to the left and right DLPFC stimulation only, which correlated with anhedonia scores. Additionally, the connectivity of the right DLPFC was significantly higher in youth depression. Source reconstruction attributed the observed connectivity dysregulation to regions belonging to the default mode network. The neurophysiological signatures identified in this study have high potential to inform the development of more effective and targeted interventions for the youth depression population.
© The Author(s) 2020. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Keywords:  EEG; TMS; adolescence; depression; youth

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Year:  2020        PMID: 32118262      PMCID: PMC7264684          DOI: 10.1093/cercor/bhaa004

Source DB:  PubMed          Journal:  Cereb Cortex        ISSN: 1047-3211            Impact factor:   5.357


  59 in total

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Authors:  Ozgur Yorbik; Boris Birmaher; David Axelson; Douglas E Williamson; Neal D Ryan
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Review 8.  Why do many psychiatric disorders emerge during adolescence?

Authors:  Tomás Paus; Matcheri Keshavan; Jay N Giedd
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10.  Task-related deactivation and functional connectivity of the subgenual cingulate cortex in major depressive disorder.

Authors:  Christopher G Davey; Murat Yücel; Nicholas B Allen; Ben J Harrison
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3.  Changes in the TMS-evoked potential N100 in the dorsolateral prefrontal cortex as a function of depression severity in adolescents.

Authors:  Lea Biermann; Heidrun Lioba Wunram; Lena Pokorny; Eva Breitinger; Nicola Großheinrich; Tomasz Antoni Jarczok; Stephan Bender
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4.  Neurophysiological markers of response to theta burst stimulation in youth depression.

Authors:  Prabhjot Dhami; Sravya Atluri; Jonathan Lee; Yuliya Knyahnytska; Paul E Croarkin; Daniel M Blumberger; Zafiris J Daskalakis; Faranak Farzan
Journal:  Depress Anxiety       Date:  2020-10-01       Impact factor: 6.505

5.  State Anhedonia in Young Healthy Adults: Psychometric Properties of the German Dimensional Anhedonia Rating Scale (DARS) and Effects of the COVID-19 Pandemic.

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6.  Using Network Parcels and Resting-State Networks to Estimate Correlates of Mood Disorder and Related Research Domain Criteria Constructs of Reward Responsiveness and Inhibitory Control.

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  6 in total

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