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Cortical and subcortical mechanisms in persistent stuttering ...

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Chapter 1 Introduction<br />

1 Introduction<br />

Stutter<strong>in</strong>g is a speech disorder that occurs without known orig<strong>in</strong> between 3 <strong>and</strong> 8 years of age<br />

<strong>and</strong> often remits before puberty. When it persists after puberty it becomes a chronic adult<br />

speech disorder throughout the lifespan (Andrews et al., 1983). The advances <strong>in</strong> neuroimag<strong>in</strong>g<br />

promoted <strong>in</strong>sights <strong>in</strong>to the highly distributed system of speech production <strong>and</strong> its alterations<br />

<strong>in</strong> adulthood stutter<strong>in</strong>g. One important motivation <strong>in</strong> stutter<strong>in</strong>g research is to separate<br />

neurobiological correlates of the core symptoms of stutter<strong>in</strong>g from neurobiological correlates<br />

associated with compensation, attempts to avoid stutter<strong>in</strong>g. Results so far <strong>in</strong>dicate a variety of<br />

complex dysfunctional systems <strong>and</strong> it appeared problematic to dist<strong>in</strong>guish between<br />

<strong>mechanisms</strong> responsible for speech dysfluencies <strong>and</strong> those connected to compensation <strong>in</strong> the<br />

adult system (Ludlow, 2000). The first study of this dissertation will tie <strong>in</strong> with this problem.<br />

Another important aspect is aga<strong>in</strong> motivated by neuroimag<strong>in</strong>g studies that stress irregularities<br />

<strong>in</strong> the activation of the primary motor cortex dur<strong>in</strong>g different functional states associated with<br />

speech production. The regulation of blood supply which is the basis of functional magnetic<br />

resonance imag<strong>in</strong>g (fMRI) is correlated with summed neuronal activity but conclusions about<br />

states of cortical excitability <strong>and</strong> thus neurophysiological <strong>mechanisms</strong> are <strong>in</strong>direct. The<br />

modulation of cortical excitability is an <strong>in</strong>herent pr<strong>in</strong>ciple <strong>in</strong> the encod<strong>in</strong>g of output signal by<br />

the primary motor cortex <strong>and</strong> the method of choice to non-<strong>in</strong>vasively study this <strong>in</strong> humans is<br />

transcranial magnetic stimulation (TMS). This method is well established <strong>in</strong> Professor Paulus’<br />

Department of Cl<strong>in</strong>ical Neurophysiology, for <strong>in</strong>stance to <strong>in</strong>vestigate neuromodulation <strong>in</strong> the<br />

primary motor cortex representation of small h<strong>and</strong> muscles. One aim of the dissertation was to<br />

establish record<strong>in</strong>gs of TMS <strong>in</strong>duced motor evoked potentials (MEPs) from facial muscles.<br />

This enabled me to conduct the first study of the <strong>in</strong>tracortical excitability of the primary<br />

tongue motor representation <strong>in</strong> adults who stutter.<br />

A sem<strong>in</strong>al work motivated the third study <strong>in</strong>cluded <strong>in</strong> this dissertation: diffusion tensor<br />

imag<strong>in</strong>g (DTI) identified reduced white matter <strong>in</strong>tegrity <strong>in</strong> fibres connect<strong>in</strong>g frontal, temporal<br />

<strong>and</strong> parietal speech related areas (Sommer et al., 2002a). Affected are possibly fibres<br />

mediat<strong>in</strong>g the mapp<strong>in</strong>g of speech sounds to articulation. The <strong>in</strong>teraction of speech production<br />

<strong>and</strong> speech perception <strong>and</strong> the <strong>in</strong>terference of stutter<strong>in</strong>g with this <strong>in</strong>teraction is the topic of the<br />

third study reported <strong>in</strong> this dissertation.<br />

Dur<strong>in</strong>g the course of my doctoral studies I furthermore contributed to a longitud<strong>in</strong>al DTI<br />

study aim<strong>in</strong>g at identify<strong>in</strong>g a biological marker of stutter<strong>in</strong>g persistency at stutter<strong>in</strong>g onset. In<br />

9

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