Examining the Complex Mismatch Negativity in Early Phase Psychosis Using the Dual Rule Paradigm.

Clinical EEG and neuroscience Pub Date : 2025-01-01 Epub Date: 2024-08-16 DOI:10.1177/15500594241273287
Jenna N Bissonnette, T-Jay Anderson, Candice E Crocker, Philip G Tibbo, Dean F Salisbury, Derek J Fisher
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Abstract

Using electroencephalography (EEG) to examine the simple mismatch negativity (MMN), a marker of auditory cortex function, has been of great interest in the exploration of biomarkers for psychotic illness. Despite many studies reporting MMN deficits in chronic schizophrenia, there are inconsistent reports of MMN reductions in the early phases of psychotic illness, suggesting the MMN elicited by traditional paradigms may not be a sensitive enough measure of vulnerability to be used as a biomarker. Recently, a more computationally complex measure of auditory cortex function (the complex mismatch negativity; cMMN) has been hypothesized to provide a more sensitive marker of illness vulnerability. The current study employed a novel dual rule paradigm, in which two pattern rules are established and violated, to examine the cMMN in 14 individuals with early phase psychosis (EPP, < 5 years illness) and 15 healthy controls (HC). Relationships between cMMN waveforms, symptom severity, and measures of functioning were explored. We found reductions of cMMN amplitudes at the site of maximal amplitude in EPP (p = .017) with large effect sizes (Hedges' g = 0.96). This study is an early step in the exploration of the cMMN as a biomarker for psychosis. Our results provide evidence that the dual rule cMMN paradigm shows promise as a method for cMMN elicitation that captures more subtle neurofunctional changes in the early stages of illness.

利用双重规则范式研究早期精神病患者的复杂错配负性。
利用脑电图(EEG)检查简单的错配负性(MMN)是听觉皮层功能的标志,在探索精神病生物标志物方面一直备受关注。尽管许多研究报告了慢性精神分裂症患者的错配负性(MMN)缺陷,但关于精神疾病早期阶段错配负性(MMN)降低的报告并不一致,这表明传统范式引起的错配负性(MMN)可能不是一种足够敏感的脆弱性测量方法,不能用作生物标记物。最近,一种在计算上更复杂的听觉皮层功能测量方法(复杂错配负性;cMMN)被认为能提供更灵敏的疾病易感性标记。目前的研究采用了一种新颖的双规则范式(即建立和违反两种模式规则),对 14 名早期精神病患者(EPP,p = .017)的 cMMN 进行了检测,并取得了较大的效应量(Hedges' g = 0.96)。这项研究是将 cMMN 作为精神病生物标记物进行探索的第一步。我们的研究结果证明,双规则 cMMN 范式有望作为一种 cMMN 激发方法,捕捉疾病早期阶段更微妙的神经功能变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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