ArticleeNeuro2024
Dissecting Mismatch Negativity: Early and Late Subcomponents for Detecting Deviants in Local and Global Sequence Regularities.
Article in eNeuro, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Speech Recognition Deficits in Presbyacusis: Links to Cortical Structural and Functional Alterations.World journal of otorhinolaryngology - head and neck surgery · 2026Article
- Alpha oscillatory activity reveals focused-attentional disparity between cochlear implant users and normal hearing listeners.Scientific reports · 2026Article
- Functional Dissociation of Mismatch Negativity From Late Discriminative Negativity Across the Adult Lifespan.The European journal of neuroscience · 2026Article
- Does Sound Timing Organization Matter? How Time Interval Influences the Perception of Closely Spaced Frequencies.Brain sciences · 2026Article
- Pre-attentive Pitch Processing of Harmonic Complex Sounds at Sensor and Source Levels: Comparing Simultaneously Recorded EEG and MEG Data.Brain topography · 2025Article
- Cortical networks with multiple interneuron types generate oscillatory patterns during predictive coding.PLoS computational biology · 2025Article
- Erroneous predictive coding across brain hierarchies in a non-human primate model of autism spectrum disorder.Communications biology · 2024Article
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Authors and funding
4 authors.
Funding
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Abstract
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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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.