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Global Motor Inhibition Precedes Stuttering Events

View ORCID ProfileJoan Orpella, View ORCID ProfileGraham Flick, View ORCID ProfileM. Florencia Assaneo, View ORCID ProfileLiina Pylkkänen, View ORCID ProfileDavid Poeppel, View ORCID ProfileEric S. Jackson
doi: https://doi.org/10.1101/2022.08.02.501857
Joan Orpella
1Department of Psychology, New York University, USA
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  • For correspondence: jo1358@nyu.edu eric.s.jackson@nyu.edu
Graham Flick
1Department of Psychology, New York University, USA
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M. Florencia Assaneo
2Institute of Neurobiology, National Autonomous University of Mexico, Juriquilla, Querétaro, Mexico
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Liina Pylkkänen
1Department of Psychology, New York University, USA
3Department of Linguistics, New York University, USA
4NYUAD Institute, New York University Abu Dhabi, United Arab Emirates
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David Poeppel
1Department of Psychology, New York University, USA
5Center for Language, Music and Emotion (CLaME), New York University, New York, NY, USA
6Ernst Strüngmann Institute (ESI) for Neuroscience, Frankfurt, Germany
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Eric S. Jackson
7Department of Communicative Sciences and Disorders, New York University, USA
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  • For correspondence: jo1358@nyu.edu eric.s.jackson@nyu.edu
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Abstract

Research points to neurofunctional differences underlying fluent speech production in stutterers and non-stutterers. There has been considerably less work focusing on the processes that underlie stuttered speech, primarily due to the difficulty of reliably eliciting stuttering in the unnatural contexts associated with neuroimaging experiments. We used magnetoencephalography (MEG) to test the hypothesis that stuttering events result from global motor inhibition–a “freeze” response typically characterized by increased beta power in nodes of the action-stopping network. We leveraged a novel clinical interview to develop participant-specific stimuli in order to elicit a comparable amount of stuttered and fluent trials. Twenty-nine adult stutterers participated. The paradigm included a cue prior to a go signal, which allowed us to isolate processes associated with stuttered and fluent trials prior to speech initiation. During this pre-speech time window, stuttered trials were associated with greater beta power in the right pre-supplementary motor area, a key node in the action-stopping network, compared to fluent trials. Beta power in the right pre-supplementary area was related to a clinical measure of stuttering severity. We also found that anticipated words identified independently by participants were stuttered more often than those generated by the researchers, which were based on the participants’ reported anticipated sounds. This suggests that global motor inhibition results from stuttering anticipation. This study represents the largest comparison of stuttered and fluent speech to date. The findings provide a foundation for clinical trials that test the efficacy of neuromodulation on stuttering. Moreover, our study demonstrates the feasibility of using our approach for eliciting stuttering during MEG and functional magnetic resonance imaging experiments so that the neurobiological bases of stuttered speech can be further elucidated.

Competing Interest Statement

The authors have declared no competing interest.

  • Abbreviations

    CBGTC
    cortico-basal ganglia-thalamocortical;
    dSPM
    dynamic statistical parameter mapping;
    MEG
    magnetoencephalography;
    R-DLPFC
    right dorsolateral prefrontal cortex;
    SSI-4
    stuttering severity index - 4th edition;
    SLP
    speech-language pathologist;
    SMA
    supplementary motor area;
    tDCS
    transcranial direct current stimulation;
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    Posted August 03, 2022.
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    Global Motor Inhibition Precedes Stuttering Events
    Joan Orpella, Graham Flick, M. Florencia Assaneo, Liina Pylkkänen, David Poeppel, Eric S. Jackson
    bioRxiv 2022.08.02.501857; doi: https://doi.org/10.1101/2022.08.02.501857
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    Global Motor Inhibition Precedes Stuttering Events
    Joan Orpella, Graham Flick, M. Florencia Assaneo, Liina Pylkkänen, David Poeppel, Eric S. Jackson
    bioRxiv 2022.08.02.501857; doi: https://doi.org/10.1101/2022.08.02.501857

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