Regional Homogeneity in schizophrenia patients with tardive dyskinesia: a resting-state fMRI study
•Regional Homogeneity of the whole brain among TDs were investigated.•TD was associated with higher regional homogeneity of Left Inferior Semilunar Lobule, a part of the neocerebellum critical to movement and cognitive control.•Higher regional homogeneity was negatively correlated with dyskinesia se...
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Veröffentlicht in: | Psychiatry research. Neuroimaging 2023-10, Vol.335, p.111724-111724, Article 111724 |
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Sprache: | eng |
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Zusammenfassung: | •Regional Homogeneity of the whole brain among TDs were investigated.•TD was associated with higher regional homogeneity of Left Inferior Semilunar Lobule, a part of the neocerebellum critical to movement and cognitive control.•Higher regional homogeneity was negatively correlated with dyskinesia severity assessed by the Abnormal Involuntary Movement Scale.
Neuronal degeneration and apoptosis may play an important role in the pathogenesis of tardive dyskinesia (TD). Previous studies suggested brain structural and functional abnormalities in patients with TD. We investigated changes in cerebral regional homogeneity (ReHo) in patients with TD using resting-state functional magnetic resonance imaging (rs-fMRI). Imaging data were collected from schizophrenia patients with TD (TD group, n=58) and without TD (non-TD group, n=66) and healthy controls (HC group, n=67), processed with SPM, and evaluated at a corrected threshold. Psychopathology and severity of TD were assessed with the Positive and Negative Syndrome Scale (PANSS) and Abnormal Involuntary Movement Scale (AIMS), respectively. Results: TD vs. non-TD group showed significantly higher ReHo in the Left Inferior Semilunar Lobule and Right Fusiform Gyrus and lower ReHo in Left Supramarginal Gyrus, Right Inferior Tempotal Gyrus, and Left Medial Frontal Gyrus. The ReHo value in the Left Inferior Semilunar Lobule was negatively correlated with AIMS upper limbs scores. Conclusions: The findings suggest altered regional neural connectivities in association with TD and may inform research of the etiology and monitor the course of TD in patients with schizophrenia and potentially other psychotic disorders. |
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ISSN: | 0925-4927 1872-7506 |
DOI: | 10.1016/j.pscychresns.2023.111724 |