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DOI 10.1007/s00406-013-0417-0

Медицинская библиотека · European archives of psychiatry and clinical neuroscience · 2013

Thalamocortical connectivity during resting state in schizophrenia.

Klingner Carsten M, Langbein Kerstin, Dietzek Maren, Smesny Stefan, Witte Otto W, Sauer Heinrich, Nenadic Igor

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Schizophrenia has been linked to disturbed connectivity between large-scale brain networks. Altered thalamocortical connectivity might be a major mechanism mediating regionally distributed dysfunction, yet it is only incompletely understood. We analysed functional magnetic resonance imaging data obtained during resting state from 22 DSM-IV schizophrenia patients and 22 matched healthy controls to directly assess the differences in thalamocortical functional connectivity. We identified significantly higher overall thalamocortical functional connectivity in patients, which was mostly accounted for by difference in thalamic connections to right ventrolateral prefrontal and bilateral secondary motor and sensory (superior temporal and lateral occipital) cortical areas. Voxelwise analysis showed group differences at the thalamic level to be mostly in medial and anterior thalamic nuclei and arising thalamocortical changes to be mostly due to higher positive correlations in prefrontal and superior temporal correlations, as well as absent negative correlations to sensory areas in patients. Our findings demonstrate that different types of thalamocortical dysfunction contribute to network alterations, including lack of inhibitory interaction attributed to the lack of significant negative thalamic/sensory cortical connections. These results emphasize the functional importance of the thalamus in the pathophysiology of schizophrenia.

Для цитирования: Klingner Carsten M, Langbein Kerstin, Dietzek Maren, Smesny Stefan, Witte Otto W, Sauer Heinrich, Nenadic Igor. Thalamocortical connectivity during resting state in schizophrenia.. European archives of psychiatry and clinical neuroscience. 2013. DOI: 10.1007/s00406-013-0417-0.

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