The Complex Pattern Mismatch Negativity as a Potential Indicator of Psychosis Across all Phases of Illness: A Meta-Analysis

被引:1
|
作者
Francis, Ashley M. [1 ]
Slaunwhite-Hay, Sydney [2 ]
Dempster, Kara [1 ]
Jaworska, Natalia [3 ,4 ]
Tibbo, Philip G. [1 ]
Fisher, Derek J. [1 ,2 ]
机构
[1] Dalhousie Univ, Dept Psychiat, Halifax, NS, Canada
[2] Mt St Vincent Univ, Dept Psychol, Halifax, NS, Canada
[3] Univ Ottawa, Inst Mental Hlth Res, Ottawa, ON, Canada
[4] Univ Ottawa, Dept Cellular & Mol Med, Ottawa, ON, Canada
关键词
schizophrenia; complex mismatch negativity; mismatch negativity; psychosis; early phase psychosis; electroencephalogram (EEG); event-related potential; MMN; cMMN; EVENT-RELATED POTENTIALS; AUDITORY SENSORY MEMORY; SCHIZOPHRENIA; MMN; HALLUCINATIONS; FREQUENCY; GLUTAMATE; DEVIANTS; REPRESENTATION; DYSFUNCTION;
D O I
10.1177/15500594241264870
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Over the past decade, there has been extensive research on the mismatch negativity (MMN) and its promise as a biomarker of illness in people with schizophrenia (SZ). Nevertheless, when attempting to assess the early stages of illness progression, the utility of MMN has been inconsistent. Recently, researchers have been investigating a more advanced MMN paradigm (the complex MMN [cMMN]) which is believed to index higher-order cognitive processing and has been suggested to be a more effective indicator of the early phases of SZ. The cMMN is defined as a paradigm that relies on alterations within a pre-established pattern of stimuli. In this meta-analysis, we investigated cMMN deficits in individuals with SZ, including an analysis involving those in the first 5 years of illness. Our search also included individuals with bipolar disorder who experience psychosis; however, no related papers were found and thus, no findings are reported. Our findings indicate a small/moderate effect (d = 0.47), suggesting that individuals with SZ exhibit reduced cMMN amplitudes compared to individuals without SZ. Interestingly, this effect seems to be more pronounced in individuals within the first 5 years of their illness (d = 0.58), suggesting that cMMN might be a more sensitive biomarker in the early phases of SZ compared to traditional paradigms.
引用
收藏
页码:72 / 82
页数:11
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