Key result
De novo Parkinson's disease is linked to an impaired central network modulating resting parasympathetic outflow.
Why the study?
The authors sought to evaluate the central autonomic network without task-based bias and assess whether this circuitry shows signs of dysregulation in the early stages of Parkinson disease.
Is the central network modulating parasympathetic outflow impaired in de novo Parkinson's disease patients compared to healthy controls?
Case-Control (n=28)
No
Is the central network modulating parasympathetic outflow impaired in de novo Parkinson's disease patients compared to healthy controls?
p-value: p=<0.05
The central network modulating parasympathetic outflow is impaired in the early clinical stages of Parkinson's disease, providing neuroimaging evidence for early dysautonomia.
May signal early dysautonomia in de novo Parkinson's; hypothesis-generating for central autonomic network imaging.
Task- and stimulus-based neuroimaging studies have begun to unveil the central autonomic network which modulates autonomic nervous system activity. In the present study, we aimed to evaluate the central autonomic network without the bias constituted by the use of a task. Additionally, we assessed whether this circuitry presents signs of dysregulation in the early stages of Parkinson's disease (PD), a condition which may be associated with dysautonomia. We combined heart-rate-variability based methods for time-varying assessments of the autonomic nervous system outflow with resting-state fMRI in 14 healthy controls and 14 de novo PD patients, evaluating the correlations between fMRI time-series and the instantaneous high-frequency component of the heart-rate-variability power spectrum, a marker of parasympathetic outflow. In control subjects, the high-frequency component of the heart-rate-variability power spectrum was significantly anti-correlated with fMRI time-series in several cortical, subcortical and brainstem regions. This complex central network was not detectable in PD patients. In between-group analysis, we found that in healthy controls the brain activation related to the high-frequency component of the heart-rate-variability power spectrum was significantly less than in PD patients in the mid and anterior cingulum, sensorimotor cortex and supplementary motor area, insula and temporal lobe, prefrontal cortex, hippocampus and in a region encompassing posterior cingulum, precuneus and parieto-occipital cortex. Our results indicate that the complex central network which modulates parasympathetic outflow in the resting state is impaired in the early clinical stages of PD.
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Tessa et al. (2019) conducted a case-control in Parkinson's disease (n=28). Parkinson's disease vs. Healthy controls was evaluated on Correlation between resting-state fMRI time-series and the instantaneous high-frequency component of the heart-rate-variability power spectrum (HF-HRV) (p=<0.05). De novo Parkinson's disease patients exhibited an impaired central network modulating parasympathetic outflow in the resting state compared to healthy controls.
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