Increase in Beta-Band Activity during Preparation for Overt Speech in Patients with Parkinson’s Disease

Sörös, Peter; Doñamayor, Nuria; Wittke, Catharina; Al‐Khaled, Mohamed; Brüggemann, Norbert; Münte, Thomas F.

doi:10.3389/fnhum.2017.00371

Cited by 8 publications

(1 citation statement)

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“…However, signals in beta band (12-30Hz) have been shown to play a role in motor planning, top-down motorauditory interactions and the production of overt speech. [39][40][41] Thus, we also examined betaband activity in this study. Furthermore, to isolate whether LD involves deficits in auditory feedback processing, we also briefly perturbed the pitch of participants' auditory feedback during sustained phonation.…”

Section: Introductionmentioning

confidence: 99%

Temporal specificity of abnormal neural oscillations during phonatory events in Laryngeal Dystonia

Kothare

Schneider²,

Mizuiri

et al. 2021

Preprint

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Laryngeal Dystonia is a debilitating disorder of voicing in which the laryngeal muscles are intermittently in spasm resulting in involuntary interruptions during speech. The central pathophysiology of laryngeal dystonia, underlying computational impairments in vocal motor control, remains poorly understood. Although prior imaging studies have found aberrant activity in the central nervous system during phonation in patients with laryngeal dystonia, it is not known at what timepoints during phonation these abnormalities emerge and what function may be impaired. To investigate this question, we recruited 22 adductor laryngeal dystonia patients (15 female, age range = 28.83-72.46 years) and 18 controls (8 female, age range = 27.40-71.34 years). We leveraged the fine temporal resolution of magnetoencephalography to monitor neural activity around glottal movement onset, subsequent voice onset and after the onset of pitch feedback perturbations. We examined event-related beta-band (12-30 Hz) and high-gamma band (65-150 Hz) neural oscillations. Prior to glottal movement onset, we observed abnormal frontoparietal motor preparatory activity. After glottal movement onset, we observed abnormal activity in somatosensory cortex persisting through voice onset. Prior to voice onset and continuing after, we also observed abnormal activity in the auditory cortex and the cerebellum. After pitch feedback perturbation onset, we observed no differences between controls and patients in their behavioural responses to the perturbation. But in patients, we did find abnormal activity in brain regions thought to be involved in the auditory feedback control of vocal pitch (premotor, motor, somatosensory and auditory cortices). Our study results confirm the abnormal processing of somatosensory feedback that has been seen in other studies. However, there were several remarkable findings in our study. First, patients have impaired vocal motor activity even before glottal movement onset, suggesting abnormal movement preparation. These results are significant because: (i) they occur before movement onset, abnormalities in patients cannot be ascribed to deficits in vocal performance, and (ii) they show that neural abnormalities in laryngeal dystonia are more than just abnormal responses to sensory feedback during phonation as has been hypothesised in some previous studies. Second, abnormal auditory cortical activity in patients begins even before voice onset, suggesting abnormalities in setting up auditory predictions before the arrival of auditory feedback at voice onset. Generally, activation abnormalities identified in key brain regions within the speech motor network around various phonation events not only provide temporal specificity to neuroimaging phenotypes in laryngeal dystonia but also may serve as potential therapeutic targets for neuromodulation.

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Section: Introductionmentioning

confidence: 99%