Evidence map›Paper›PMID 29093672›Full record

ArticleFrontiers in human neuroscience2017

Directed Motor-Auditory EEG Connectivity Is Modulated by Music Tempo.

Nicoletta Nicolaou, Asad Malik, Ian Daly, James Weaver, Faustina Hwang, Alexis Kirke, Etienne B Roesch, Duncan Williams, Eduardo R Miranda, Slawomir J Nasuto

Abstract read
In one paragraph

Article in Frontiers in human neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Neural decoding of music from the EEG.Scientific reports · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Effects of the Musical Sound Environment on Communicating Emotion.International journal of environmental research and public health · 2020
    Article
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Nicoletta NicolaouBrain Embodiment Laboratory, Biomedical Engineering Section, School of Biological Sciences, University of Reading, Reading, United Kingdom.
Asad MalikBrain Embodiment Laboratory, Biomedical Engineering Section, School of Biological Sciences, University of Reading, Reading, United Kingdom.
Ian DalyBrain-Computer Interfacing and Neural Engineering Laboratory, Department of Computer Science and Electronic Engineering, University of Essex, Colchester, United Kingdom.
James WeaverBrain Embodiment Laboratory, Biomedical Engineering Section, School of Biological Sciences, University of Reading, Reading, United Kingdom.
Faustina HwangBrain Embodiment Laboratory, Biomedical Engineering Section, School of Biological Sciences, University of Reading, Reading, United Kingdom.
Alexis KirkeInterdisciplinary Centre for Computer Music Research, University of Plymouth, Plymouth, United Kingdom.
Etienne B RoeschSchool of Psychology, University of Reading, Reading, United Kingdom.
Duncan WilliamsInterdisciplinary Centre for Computer Music Research, University of Plymouth, Plymouth, United Kingdom.
Eduardo R MirandaInterdisciplinary Centre for Computer Music Research, University of Plymouth, Plymouth, United Kingdom.
Slawomir J NasutoBrain Embodiment Laboratory, Biomedical Engineering Section, School of Biological Sciences, University of Reading, Reading, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Beat perception is fundamental to how we experience music, and yet the mechanism behind this spontaneous building of the internal beat representation is largely unknown. Existing findings support links between the tempo (speed) of the beat and enhancement of electroencephalogram (EEG) activity at tempo-related frequencies, but there are no studies looking at how tempo may affect the underlying long-range interactions between EEG activity at different electrodes. The present study investigates these long-range interactions using EEG activity recorded from 21 volunteers listening to music stimuli played at 4 different tempi (50, 100, 150 and 200 beats per minute). The music stimuli consisted of piano excerpts designed to convey the emotion of "peacefulness". Noise stimuli with an identical acoustic content to the music excerpts were also presented for comparison purposes. The brain activity interactions were characterized with the imaginary part of coherence (iCOH) in the frequency range 1.5-18 Hz (δ, θ, α and lower β) between all pairs of EEG electrodes for the four tempi and the music/noise conditions, as well as a baseline resting state (RS) condition obtained at the start of the experimental task. Our findings can be summarized as follows: (a) there was an ongoing long-range interaction in the RS engaging fronto-posterior areas; (b) this interaction was maintained in both music and noise, but its strength and directionality were modulated as a result of acoustic stimulation; (c) the topological patterns of iCOH were similar for music, noise and RS, however statistically significant differences in strength and direction of iCOH were identified; and (d) tempo had an effect on the direction and strength of motor-auditory interactions. Our findings are in line with existing literature and illustrate a part of the mechanism by which musical stimuli with different tempi can entrain changes in cortical activity.

Indexed as

brain connectivity analysiscoherence analysiselectroencephalography (EEG)imaginary coherencymusic tempo

Identifiers

PMID29093672
PMCPMC5651276

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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.