Do deficits in the magnocellular priming underlie visual derealization phenomena?: preliminary neurophysiological and self-report results in first-episode schizophrenia patients
Background: Early visual impairments probably partially caused by impaired interactions between magnocellular (M) and parvocellular (P) pathways (M priming deficit), and disturbances of basic self-awareness or self-disorders (SDs) are core features of schizophrenia. The relationships between these fe...
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| Hauptverfasser: | , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
17 September 2014
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| In: |
Schizophrenia research
Year: 2014, Jahrgang: 159, Heft: 2-3, Pages: 441-449 |
| ISSN: | 1573-2509 |
| DOI: | 10.1016/j.schres.2014.08.019 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.schres.2014.08.019 Verlag, lizenzpflichtig, Volltext: https://linkinghub.elsevier.com/retrieve/pii/S0920996414004551 
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| Verfasserangaben: | D. Núñez, R. Oelkers-Ax, S. de Haan, M. Ludwig, H. Sattel, F. Resch, M. Weisbrod, T. Fuchs |
MARC
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| 245 | 1 | 0 | |a Do deficits in the magnocellular priming underlie visual derealization phenomena? |b preliminary neurophysiological and self-report results in first-episode schizophrenia patients |c D. Núñez, R. Oelkers-Ax, S. de Haan, M. Ludwig, H. Sattel, F. Resch, M. Weisbrod, T. Fuchs |
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| 520 | |a Background: Early visual impairments probably partially caused by impaired interactions between magnocellular (M) and parvocellular (P) pathways (M priming deficit), and disturbances of basic self-awareness or self-disorders (SDs) are core features of schizophrenia. The relationships between these features have not yet been studied. We hypothesized that the M priming was impaired in first-episode patients and that this deficit was associated with visual aspects of SDs. Aim: To investigate early visual processing in a sample of first-episode schizophrenia patients and to explore the relationships between M and P functioning and visual aspects of SDs addressed by the Examination of Anomalous Self-Experience (EASE) interview. - Method: Nine stimulating conditions were used to investigate M and P pathways and their interaction in a pattern reversal visually evoked potential (VEP) paradigm. N80 at mixed M- and P-conditions was used to investigate magnocellular priming. Generators were analyzed using source localization (Brain Electrical Source Analysis software: BESA). VEPs of nineteen first-episode schizophrenia patients were compared to those of twenty matched healthy controls by a bootstrap resample procedure. Visual aspects of SDs were analyzed through a factor analysis to separate symptom clusters of derealization phenomena. Thereafter, the associations between the main factors and the N80 component were explored using linear mixed models. - Results: Factor analyses separated two EASE factors (“distance to the world”, and “intrusive world”). The N80 component was represented by a single dipole located in the occipital visual cortex. The bootstrap analysis yielded significant amplitude reductions and prolonged latencies in first-episode patients relative to controls in response to mixed M-P conditions, and normal amplitudes and latencies in response to isolated P- and M-biased stimulation. Exploratory analyses showed significant negative correlations between the N80 amplitude values at mixed M-P conditions and the EASE factor “distance to the world”, i.e. relatively higher amplitudes in the patient group were associated with higher subjective perceived derealization (“distance to the world”). - Conclusions: The early VEP component N80 evoked by mixed M-P conditions is assumed to be a correlate of M priming, and showed reduced amplitudes and longer latencies in first-episode patients. It probably reflects a hypoactivation of the M-pathway. The negative association between visual SDs (derealization phenomena characterized by visual experiences of being more distant to the world), and the M priming deficit was counterintuitive. It might indicate a dysregulated activity of the M-pathway in patients with SDs. Further research is needed to better understand this preliminary finding. | ||
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