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Projekt Druckansicht

Neurologische Soft Signs als externe Marker neuronaler Dysfunktion bei schizophrenen Psychosen: Untersuchungen mit multimodaler Magnetresonanztomographie

Fachliche Zuordnung Biologische Psychiatrie
Förderung Förderung von 2016 bis 2019
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 319937632
 
Erstellungsjahr 2022

Zusammenfassung der Projektergebnisse

At the beginning of the 20th century, many authors proposed that a considerable number of schizophrenia patients experience genuine sensorimotor abnormalities. Recent evidence suggests that the association between psychotic symptoms and sensorimotor abnormalities in SSD reflects neuronal dysfunction in the cortico-cerebellar-thalamo-cortical circuit (CCTCC) as conceptualized in the model of “cognitive dysmetria”. If this dysfunction develops earlier than prodromal symptoms of the disorder, it might give rise to subtle sensorimotor abnormalities. In this context, subtle sensorimotor deficits such NSS have been suggested to be an external marker of underlying neuronal dysfunction that is linked with an elevated risk for developing schizophrenia. In this project we have advanced our understanding of both NSS and other more severe sensorimotor abnormalities (e.g. parkinsonism and catatonia) in SSD. The following are the four main findings of the project: (1) Our results support the notion that NSS are not significantly modulated by current antipsychotic dosage in SSD. The associations between NSS, akathisia and parkinsonism, as revealed by this project, support the genuine rather than medication-dependent origin of particular motor abnormalities in SSD. (2) Using mCCA + jICA, we found complex neural pathomechanisms underlying NSS in SSD suggesting aberrant structure and function, predominantly in cortical and cerebellar systems that critically subserve sensorimotor dynamics and psychomotor organization. (3) Our results suggest that NSS are significant predictors of poor clinical outcome in SSD at baseline and >6 months after an acute psychotic episode. These findings propose sensorimotor domain as state biomarker of SSD and support its predictive power with respect to treatment outcome. (4) NSS scores “integrative function” and right inferior parietal lobule regional homogeneity (ReHo) were significant predictors of auditory verbal hallucinations (AVH) in SSD. These data suggest significant interrelationships between sensorimotor integration abilities, brain structure and function, and AVH symptom expression. (5) Structural reorganization of white matter bundles connecting orbitofrontal/parietal, thalamic and striatal regions contribute to catatonia in SSD patients. Overall, this interdisciplinary project used multimodal neuroimaging methods and clinical as well as behavioral assessments to better understand the role of the sensorimotor domain in the development and treatment of schizophrenia spectrum disorders. This project has provided the theoretical basis for other projects examining the sensorimotor domain in psychiatric disorders.

Projektbezogene Publikationen (Auswahl)

 
 

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