Pitch and Duration Mismatch Negativity and Premorbid Intellect in the First Hospitalized Schizophrenia Spectrum

被引:56
|
作者
Salisbury, Dean F. [1 ]
Polizzotto, Nicola R. [1 ,4 ]
Nestor, Paul G. [2 ]
Haigh, Sarah M. [1 ]
Koehler, Justine [1 ]
McCarley, Robert W. [3 ]
机构
[1] Univ Pittsburgh, Sch Med, Western Psychiat Inst & Clin, Clin Neurophysiol Res Lab, 3501 Forbes Ave,Suite 420, Pittsburgh, PA 15213 USA
[2] Univ Massachusetts, Dept Psychol, Boston, MA 02125 USA
[3] Harvard Med Sch, Dept Psychiat, VA Boston Healthcare Syst, Brockton, MA USA
[4] Univ Texas Hlth Sci Ctr Houston, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
biomarker; psychosis; first episode; sensory memory; IQ matching; MULTI-FEATURE PARADIGM; ULTRA-HIGH-RISK; 1ST-EPISODE SCHIZOPHRENIA; NEUROPSYCHOLOGICAL FUNCTION; AUDITORY HALLUCINATIONS; NEUROCOGNITIVE DEFICITS; PSYCHOSIS; ONSET; DETERIORATION; INDIVIDUALS;
D O I
10.1093/schbul/sbw074
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Mismatch negativity (MMN) is a robustly abnormal brainwave in chronically ill schizophrenia that has generated interest as a disease presence biomarker. Reports of MMN reduction in first-episode schizophrenia have been equivocal, raising uncertainty about its reduction at first psychotic break. Here we tested 29 schizophrenia- spectrum participants under 1 year from their first hospitalization for psychosis and 40 age-, gender-, parental socioeconomic status-, and Wechsler Adult Intelligence Scales III Information-matched healthy controls on both pitch and duration MMN. Participants performed a visual checkerboard tracking task while standard (1 kHz, 50 ms, 80%), pitch-deviant (1.2 kHz, 50 ms, 10%) and duration-deviant (1 kHz, 100 ms, 10%) tones were presented over headphones (75 dB) and EEG was recorded. Independent component analysis was used to remove eye movements and visual stimulus processing activity. Groups did not differ in pitch MMN or duration MMN amplitudes. Smaller pitch and duration MMN amplitudes were associated with lower estimates of premorbid intellect in all participants and independently with greater positive symptoms in first hospitalized schizophrenia. Overall MMN reduction was not present in these relatively high functioning individuals at the first episode of schizophrenia, and therefore is not a good disease presence biomarker for this sample. Future research is warranted to determine the degree of MMN reduction at the first episode of psychosis across a greater range of cognitive impairment, the utility of MMN as an indicator of risk or diagnosis, and its role for understanding pathophysiological mechanisms in emerging psychosis.
引用
收藏
页码:407 / 416
页数:10
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