Resting-state functional MRI in depression unmasks increased connectivity between networks via the dorsal nexus

To better understand intrinsic brain connections in major depression, we used a neuroimaging technique that measures resting state functional connectivity using functional MRI (fMRI). Three different brain networks—the cognitive control network, default mode network, and affective network—were inves...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 107; no. 24; pp. 11020 - 11025
Main Authors Sheline, Yvette I., Price, Joseph L., Yan, Zhizi, Mintun, Mark A., Raichle, Marcus E.
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences 15.06.2010
National Acad Sciences
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Summary:To better understand intrinsic brain connections in major depression, we used a neuroimaging technique that measures resting state functional connectivity using functional MRI (fMRI). Three different brain networks—the cognitive control network, default mode network, and affective network—were investigated. Compared with controls, in depressed subjects each of these three networks had increased connectivity to the same bilateral dorsal medial prefrontal cortex region, an area that we term the dorsal nexus. The dorsal nexus demonstrated dramatically increased depression-associated fMRI connectivity with large portions of each of the three networks. The discovery that these regions are linked together through the dorsal nexus provides a potential mechanism to explain how symptoms of major depression thought to arise in distinct networks—decreased ability to focus on cognitive tasks, rumination, excessive self-focus, increased vigilance, and emotional, visceral, and autonomic dysregulation—could occur concurrently and behave synergistically. It suggests that the newly identified dorsal nexus plays a critical role in depressive symptomatology, in effect "hot wiring" networks together; it further suggests that reducing increased connectivity of the dorsal nexus presents a potential therapeutic target.
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Edited by Marcus E. Raichle, Washington University, St. Louis, MO, and approved April 28, 2010 (received for review January 12, 2010)
Author contributions: Y.I.S. and M.A.M. designed research; Y.I.S. and Z.Y. performed research; Y.I.S. and Z.Y. analyzed data; and Y.I.S., J.L.P., and M.A.M. wrote the paper.
ISSN:0027-8424
1091-6490
1091-6490
DOI:10.1073/pnas.1000446107