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Resting-State Hyperperfusion of the Supplementary Motor Area in Catatonia

Walther, Sebastian ; Schäppi, Lea ; Federspiel, Andrea ; Bohlhalter, Stephan ; Wiest, Roland ; Strik, Werner ; Stegmayer, Katharina

In: Schizophrenia Bulletin, 2017, vol. 43, no. 5, p. 972-981

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    Titre
    • Resting-State Hyperperfusion of the Supplementary Motor Area in Catatonia
    Auteur
    • Walther, Sebastian. Translational Research Center, University Hospital of Psychiatry, Bern, Switzerland
    • Schäppi, Lea. Translational Research Center, University Hospital of Psychiatry, Bern, Switzerland
    • Federspiel, Andrea. Translational Research Center, University Hospital of Psychiatry, Bern, Switzerland
    • Bohlhalter, Stephan. Neurology and Neurorehabilitation Center, Luzerner Kantonsspital, Lucerne, Switzerland
    • Wiest, Roland. Support Center of Advanced Neuroimaging (SCAN), University Institute of Diagnostic and Interventional Neuroradiology, Inselspital, Bern, Switzerland
    • Strik, Werner. Translational Research Center, University Hospital of Psychiatry, Bern, Switzerland
    • Stegmayer, Katharina. Translational Research Center, University Hospital of Psychiatry, Bern, Switzerland
    Type de document
    • Postprint
    Langue
    • Anglais
    Publié dans
    • Schizophrenia Bulletin, 2017, vol. 43, no. 5, p. 972-981. Oxford University Press
    Autre version électronique
    Identifiant OAI-PMH
    • oai:doc.rero.ch:331995
    Summary
    Catatonia is a psychomotor syndrome that not only frequently occurs in the context of schizophrenia but also in other conditions. The neural correlates of catatonia remain unclear due to small-sized studies. We therefore compared resting-state cerebral blood flow (rCBF) and gray matter (GM) density between schizophrenia patients with current catatonia and without catatonia and healthy controls. We included 42 schizophrenia patients and 41 controls. Catatonia was currently present in 15 patients (scoring >2 items on the Bush Francis Catatonia Rating Scale screening). Patients did not differ in antipsychotic medication or positive symptoms. We acquired whole-brain rCBF using arterial spin labeling and GM density. We compared whole-brain perfusion and GM density over all and between the groups using 1-way ANCOVAs (F and T tests). We found a group effect (F test) of rCBF within bilateral supplementary motor area (SMA), anterior cingulate cortex, dorsolateral prefrontal cortex, left interior parietal lobe, and cerebellum. T tests indicated 1 cluster (SMA) to be specific to catatonia. Moreover, catatonia of excited and retarded types differed in SMA perfusion. Furthermore, increased catatonia severity was associated with higher perfusion in SMA. Finally, catatonia patients had a distinct pattern of GM density reduction compared to controls with prominent GM loss in frontal and insular cortices. SMA resting-state hyperperfusion is a marker of current catatonia in schizophrenia. This is highly compatible with a dysregulated motor system in catatonia, particularly affecting premotor areas. Moreover, SMA perfusion was differentially altered in retarded and excited catatonia subtypes, arguing for distinct pathobiology.