The recent discovery of "inter-effector" areas (IEAs) interleaved between the classic effector-specific regions of primary motor cortex is reshaping how we understand the motor circuits that support fluent speech - and where they break down in stuttering. This project applies, for the first time in stuttering, precision MRI mapping to chart these circuits at the level of the individual.
In Aim 1, precision MRI localizes individual-specific IEAs and characterizes their structural and resting-state functional connectivity in relation to each person's behavioral, cognitive, and emotional profile. In Aim 2, the activity and connectivity of the IEAs are examined during ecologically valid continuous-speech tasks. In Aim 3, the work asks whether these nodes and connections deviate during a developmentally sensitive period for speech and language. Together, the aims work toward identifying specific, individualized targets for future treatment and preventive intervention.
Subawards: Ho Ming Chow, PhD (University of Delaware), continuous-speech fMRI; Caterina Gratton, PhD (University of Illinois Urbana-Champaign), precision functional mapping.
This research is funded through an NIDCD/NIH grant R01 DC022763 (PI Chang).
This study involves collecting longitudinal data (behavioral, neuroimaging) from young children who stutter and their age-matched peers, starting from close to stuttering onset (ages 3 and up). Multiple acquisition of these data points from each child enables us to examine brain developmental trajectories that differ between children who do and do not stutter, and further help elucidate factors that are associated with persistent forms of stuttering. We are also investigating how brain and behavioral changes that correlate with persistent developmental stuttering differ between the two sexes.
These analyses will help us answer some long-standing questions about stuttering, such as: Why do some children recover naturally from stuttering while others don't? Why do more boys stutter than girls?
The findings from this research have potential to lead to early objective prognostic markers for persistent stuttering, elucidate neural subtypes, and pave the way for neuroscience-based treatment development.
This research is funded through an NIDCD/NIH grant R01 DC011277 (PI Chang).
The treatments that are available to people who stutter are limited and don’t work for everybody. There is an urgent need to develop updated treatment options that are based on our current neuroscientific understanding of stuttering. Because stuttering begins in childhood, behavioral interventions need to be developmentally appropriate for children and engaging enough to hold their attention. This project will develop a rhythm-based game and then pilot the game with children who stutter to determine whether rhythm games are a viable treatment option that can improve stuttering severity and persistence.
In collaboration with Devin McAuley, Ph.D., Professor of Cognition and Cognitive Neuroscience at Michigan State University and Say-It Labs, a therapeutic gaming company, the digital game will guide players through progressively complex rhythm training activities. The game design will apply what we have already observed through studying structural and functional connectivity in the brains of children who stutter.
Research has shown an association between deficits in the basal ganglia thalamocortical (BGTC) network and stuttering onset and persistence. The BGTC network supports timing and initiation of speech movements necessary for fluent speech. This network is also thought to play a role in enabling the brain to synchronize with rhythmic patterns in the environment to support “beat-based” timing, which relies on medial timing structures such as the putamen and the supplementary motor area. In children who stutter, behavioral deficits in beat-based timing have been observed as well as structural and functional connectivity deficits in medial timing structures. Together, this raises the question of whether a game targeted at enhancing rhythm processing and internal beat generation in children who stutter could improve these deficits, in turn supporting improved motor control and facilitating fluent speech.
Findings from developing and piloting this game are expected to build a strong foundation for breakthroughs in the development of neuroscience-guided treatments for stuttering. This is significant because it directly addresses the critical lack of effective treatment options available.
This research is funded through an NIDCD/NIH grant R01. (PI: Chang)
Examining neural oscillations -- rhythmic fluctuations of neural excitability -- provides an opportunity to better understand the neurophysiological bases of the auditory-motor coordination deficits that have been reported in stuttering speakers. Fluent speech requires coordinated neuronal activity that is achieved through neural oscillatory synchrony across brain structures. The overall objective of this study is to determine how children who stutter (CWS) differ from fluent peers in neural oscillatory synchrony across auditory-motor structures during speech perception, planning, and production under two conditions - with and without rhythmic entrainment. Guided by EEG and MRI data collected from children who do and do not stutter, our central hypothesis is that beta oscillations, which control predictive timing of movements through coordination of motor to auditory systems, will show aberrant power, reduced inter-trial phase clustering, and reduced interregional oscillatory phase synchrony in CWS. A better understanding in this area has exciting treatment implications, since manipulation of synchrony within oscillatory patterns in auditory-motor systems may be possible through entrainment with external sensory stimuli and non-invasive brain stimulation. This project will thus allow us to lay the groundwork towards systematic, neurobiology-based intervention development for CWS. This research will be the first series of studies designed to characterize neural oscillatory synchrony specific to speech processing in CWS, which may serve as a highly predictive neural marker for persistent stuttering during early childhood. The findings are expected to elucidate, for the first time, causal mechanisms behind auditory-motor integration deficits in persistent stuttering. Such results will have an important positive impact, as the identified neural mechanisms underlying fluent speech will lay the foundation for effective early intervention for stuttering.
This research is funded through an NIDCD/NIH R01 grant R01DC018283 (PI: Chang)
Many models of speech timing have proposed that speech, like other motor activities, is rhythmically structured in time. Rhythm can be defined as a pattern of durations marked by a series of events, and perceptually as the temporal organization of the physical sound pattern. One of the hallmarks of skilled motor behavior such as fluent speech production is accurate timing, and the possible critical role of aberrant temporal processing in stuttering has been one of the oldest and most dominant perspectives in the field. However, studies examining temporal processing in children who stutter have been rare. In our studies, we have used a rhythm perception task (auditory perceptual timing) to show that children who stutter exhibit significantly reduced rhythm discrimination performance compared to controls. The task relies on the ability to perceive the temporal organization of a sequence of tones, which taxes intrinsic timing ability (i.e., internal generation of a beat) without the confounding effects of speech production. CWS showed poorer rhythm discrimination relative to controls, especially in the complex condition where the “beats” occurring in rhythms are not explicitly marked and hence require greater internal generation of timing. In addition, CWS showed aberrant brain connectivity involving the cortico-BG networks, and a negative correlation between rhythm discrimination performance and functional connectivity of basal ganglia (BG) and cerebellum (CE). In terms of rhythm production (motor timing), the extant data are conflicting, for example based on tapping task performance in adults who stutter. Examining the relationship between performance on temporal processing tasks and brain connectivity in the “timing networks” that involve both BG and CE circuits is expected to provide breakthroughs in our understanding of the neurobiological bases of timing control deficits that may underlie persistent developmental stuttering.
Combining neuroimaging and behavioral experiments that involve rhythm perception and production tasks, we are conducting parallel series of studies to investigate a novel rhythm deficit hypothesis in stuttering. This study is in collaboration with Drs. Devin McAuley at Michigan State University.
This study is funded by the NIDCD/NIH grant R01 DC011277 (PI Chang), Grammy Foundation and the RAIND (Research in Autism, Intellectual, and Neurodevelopmental Disabilities) pilot grant (PIs McAuley, Chang, Wade, Dilley).
We are fortunate to work with outstanding collaborators across the country:
Frank H. Guenther, PhD - Boston University: speech motor-control modeling (DIVA/GODIVA); subcontract partner (R01 DC007683).
Ho Ming Chow, PhD - University of Delaware: continuous-speech fMRI and neural subtypes; subcontract partner (R01 DC020157) and Co-I on the motor cortical circuits project (R01 DC022763).
Caterina Gratton, PhD - University of Illinois Urbana-Champaign: precision functional brain mapping; Co-I on the motor cortical circuits project (R01 DC022763).
J. Devin McAuley, PhD - Michigan State University: rhythm and timing in speech and music; multiple-PI on the Digital Rhythm Games project.
Amanda Hampton Wray, PhD - University of Pittsburgh: EEG and neural oscillatory markers in children who stutter; subcontract partner (R01 DC019904).