Duration and frequency mismatch negativity shows no progressive reduction in early stages of psychosis

被引:26
作者
Koshiyama, Daisuke [1 ]
Kirihara, Kenji [1 ]
Tada, Mariko [1 ]
Nagai, Tatsuya [1 ,2 ]
Koike, Shinsuke [1 ,3 ,4 ]
Suga, Motomu [1 ,5 ]
Araki, Tsuyoshi [6 ]
Kasai, Kiyoto [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Neuropsychiat, Tokyo, Japan
[2] Kawamuro Mem Hosp, Dept Psychiat, Niigata, Japan
[3] UTIDAHM, Tokyo, Japan
[4] Univ Tokyo, Grad Sch Art & Sci, Ctr Evolutionary Cognit Sci, Tokyo, Japan
[5] Univ Tokyo, Grad Sch Med, Dept Rehabil, Tokyo, Japan
[6] Univ Tokyo, Grad Sch Med, Dept Youth Mental Hlth, Tokyo, Japan
关键词
MMN; Longitudinal study; Schizophrenia; Ultra-high risk; First-episode psychosis; Biomarker; ULTRA-HIGH-RISK; CLINICAL HIGH-RISK; UNTREATED PSYCHOSIS; BREAKTHROUGH BIOMARKER; 1ST-EPISODE PSYCHOSIS; PREDICTING PSYCHOSIS; SCHIZOPHRENIA; DEFICITS; INDIVIDUALS; ONSET;
D O I
10.1016/j.schres.2017.03.015
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
The auditory mismatch negativity (MMN) is a component of event-related potentials, which is being increasingly recognized as a candidate biomarker for early stages of psychosis. Although previous cross-sectional studies have demonstrated small MMN amplitude in early stages of psychosis, it remains unknown whether small MMN amplitude is due to progressive reduction during the early course. In this study, we investigated longitudinal changes of MMN in early stages of psychosis. Participant included 14 patients with first-episode psychosis (FEP), 16 individuals with ultra-high risk (UHR), and 16 healthy control subjects (HC). We measured MMN in response to duration deviants (dMMN) and that in response to frequency deviants (fMMN), respectively. The amplitudes of dMMN in FEP and UHRwere significantly smaller in comparison to those in HC, which did not show a progressive decrease over time. The amplitude of fMMN did not differ among groups, which again did not show progression. There was no significant correlation between the length of the follow-up period and the longitudinal change of either deviant-type MMN in the FEP or UHR. These results suggest that dMMN is a trait marker in the early stages of psychosis, and that small dMMN amplitude in early stages of psychosis may reflect altered developmental process rather than progressive brain pathology. The amplitude of fMMN may not alter in early stages of psychosis. These findings may contribute to the future establishment of MMN as a biomarker in early stages of psychosis. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 38
页数:7
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