Different patterns of auditory information processing deficits in chronic schizophrenia and bipolar disorder with psychotic features

被引:23
|
作者
Domjan, Nora [1 ]
Csifcsak, Gabor [2 ]
Drotos, Gergely [1 ]
Janka, Zoltan [1 ]
Szendi, Istvan [1 ]
机构
[1] Univ Szeged, Dept Psychiat, Fac Med, Albert Szent Gyorgyi Med & Pharmaceut Ctr, H-6725 Szeged, Hungary
[2] Univ Szeged, Inst Psychol, Fac Arts, H-6722 Szeged, Hungary
关键词
Schizophrenia; Bipolar disorder; P50; N100; Mismatch negativity; P3b; EVENT-RELATED POTENTIALS; MISMATCH NEGATIVITY MMN; NEUROPHYSIOLOGICAL ENDOPHENOTYPES; ELECTROPHYSIOLOGICAL INDEXES; EVOKED POTENTIALS; GENETIC OVERLAP; META-STRUCTURE; DSM-V; P50; P300;
D O I
10.1016/j.schres.2012.06.002
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
With the development of DSM-V and ICD-11 the definitions of psychiatric disorders are under re-evaluation. The emphasis is shifted from distinct disorders to clusters defined not only by symptomatology, but also by underlying neurobiology and cognitive deficits. Bipolar disorder I (BD-I) and schizophrenia (SZ) are of special interest since their differential diagnosis is often problematic and they partially overlap in measures ranging from genetics to neurophysiology. Event-related potentials (ERPs) are one of the most studied factors but the results are still controversial, primarily in BD-I, where ERPs reflecting different stages of auditory information processing have been much less investigated. In this study, we aimed at investigating the changes of five auditory event-related potentials (P50 and N100 suppression, duration and pitch deviant mismatch negativity (MMN) and P3b) in 20 SZ and 20 BD-I patients with a history of psychosis and 21 healthy control subjects. Our data revealed substantial differences between the two patient groups. Only patients with SZ demonstrated impaired N100 suppression, shorter duration deviant MMN latency and attenuated P3b amplitude, while prolonged pitch deviant MMN latency was found to be characteristic of the BD-I group. No shared ERP abnormalities were observed among the patient groups. Our results indicate that SZ and BD-I are characterized by highly different neurophysiological profiles when measured in the same laboratory setting. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:253 / 259
页数:7
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