Dissecting Mismatch Negativity: Early and Late Subcomponents for Detecting Deviants in Local and Global Sequence Regularities

被引:1
作者
Huang, Yiyuan Teresa [1 ,2 ,3 ]
Wu, Chien-Te [1 ,2 ]
Koike, Shinsuke [1 ,3 ,4 ]
Chao, Zenas C. [1 ]
机构
[1] Univ Tokyo, UTIAS, Int Res Ctr Neurointelligence WPI IRCN, Tokyo 1130033, Japan
[2] Natl Taiwan Univ, Coll Med, Sch Occupat Therapy, Taipei 100, Taiwan
[3] Univ Tokyo, Grad Sch Arts & Sci, Dept Multidisciplinary Sci, Tokyo 1538902, Japan
[4] Univ Tokyo Inst Divers & Adaptat Human Mind UTIDAH, Tokyo 1130033, Japan
关键词
EEG; hierarchy; mismatch negativity; predictive coding; subcomponents; AUDITORY CHANGE-DETECTION; PREFRONTAL CORTEX; STIMULUS DEVIANCE; SCHIZOPHRENIA; MMN; PROBABILITY; MODEL; ERP; DYSFUNCTION; COMPONENTS;
D O I
10.1523/ENEURO.0050-24.2024
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mismatch negativity (MMN) is commonly recognized as a neural signal of prediction error evoked by deviants from the expected patterns of sensory input. Studies show that MMN diminishes when sequence patterns become more predictable over a longer timescale. This implies that MMN is composed of multiple subcomponents, each responding to different levels of temporal regularities. To probe the hypothesized subcomponents in MMN, we record human electroencephalography during an auditory local-global oddball paradigm where the tone-to-tone transition probability (local regularity) and the overall sequence probability (global regularity) are manipulated to control temporal predictabilities at two hierarchical levels. We find that the size of MMN is correlated with both probabilities and the spatiotemporal structure of MMN can be decomposed into two distinct subcomponents. Both subcomponents appear as negative waveforms, with one peaking early in the central-frontal area and the other late in a more frontal area. With a quantitative predictive coding model, we map the early and late subcomponents to the prediction errors that are tied to local and global regularities, respectively. Our study highlights the hierarchical complexity of MMN and offers an experimental and analytical platform for developing a multitiered neural marker applicable in clinical settings.
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页数:10
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