ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2022
Cross-Frequency Brain Network Dynamics Support Pitch Change Detection.
Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2022. 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, 9 citations in OpenAlex.
- Frequency-Specific Neural Dynamics and Decoding of Hierarchical Auditory Sequences Revealed by Magnetoencephalography.Neuroscience bulletin · 2026Article
- Atypical Change Detection in Sound Sequences: A Behavioral and Magnetoencephalography Study in Congenital Amusia.The European journal of neuroscience · 2026Article
- Auditory neural entrainment: frequency-specific functional roles and emerging applications in neurological and psychiatric disorders.Frontiers in human neuroscience · 2026Review
- Beyond pitch: temporal processing deficits in congenital amusia.Psychological research · 2025Article
- Human Auditory-Motor Networks Show Frequency-Specific Phase-Based Coupling in Resting-State MEG.Human brain mapping · 2025Article
- EEG analysis of speaking and quiet states during different emotional music stimuli.Frontiers in neuroscience · 2025Article
- Cross-frequency coupling in cortico-hippocampal networks supports the maintenance of sequential auditory information in short-term memory.PLoS biology · 2024Article
Corrections and comments
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Authors and funding
6 authors at 3 institutions in 3 countries.
Funding
Abstract
Processing auditory sequences involves multiple brain networks and is crucial to complex perception associated with music appreciation and speech comprehension. We used time-resolved cortical imaging in a pitch change detection task to detail the underlying nature of human brain network activity, at the rapid time scales of neurophysiology. In response to tone sequence presentation to the participants, we observed slow inter-regional signaling at the pace of tone presentations (2-4 Hz) that was directed from auditory cortex toward both inferior frontal and motor cortices. Symmetrically, motor cortex manifested directed influence onto auditory and inferior frontal cortices via bursts of faster (15-35 Hz) activity. These bursts occurred precisely at the expected latencies of each tone in a sequence. This expression of interdependency between slow/fast neurophysiological activity yielded a form of local cross-frequency phase-amplitude coupling in auditory cortex, which strength varied dynamically and peaked when pitch changes were anticipated. We clarified the mechanistic relevance of these observations in relation to behavior by including a group of individuals afflicted by congenital amusia, as a model of altered function in processing sound sequences. In amusia, we found a depression of inter-regional slow signaling toward motor and inferior frontal cortices, and a chronic overexpression of slow/fast phase-amplitude coupling in auditory cortex. These observations are compatible with a misalignment between the respective neurophysiological mechanisms of stimulus encoding and internal predictive signaling, which was absent in controls. In summary, our study provides a functional and mechanistic account of neurophysiological activity for predictive, sequential timing of auditory inputs.
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