Can Postural Instability Respond to Galvanic Vestibular Stimulation in Patients with Parkinson’s Disease?

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Abstract

MATERIALS & METHODS

All 5 patients fulfilled the UK Parkinson’s Disease Society Brain Bank criteria [8]. Two patients had mild lateral trunk flexion, and the other three patients had camptocormia. No patient had a history of neurosurgery or otorhinolaryngeal illness.

Binaural monopolar GVS was performed using devices described previously (Chattanooga Intelect Advanced Combo, DJO Global, Vista, CA, USA) [3,4]. In patients with a lateral trunk flexion, binaural bipolar GVS was used, i.e., a 10.2-cm² cathode electrode was located ipsilateral to the lateral trunk flexion, and a 10.2-cm² anode electrode was located on the contralateral side. In the patient with a camptocormia, pairs of 10.2-cm² cathode and anode electrodes were placed over both mastoid processes and trapezius muscles. The current intensity was increased to 0.7 mA, and the current was applied for 20 minutes with the patient in the supine position. For the sham stimulation, the first procedure was same, but the current intensity was subsequently ramped down to 0 mA over the course of 10 seconds, and this status was continued for 20 minutes. Either one of these procedures was randomly assigned to each patient. At the same time, 1 week after the initial procedure the other procedure was performed again in the same patient. Neurologists who were blind to all clinical information and the status of GVS performed a pull test according to item 12 of the revised UPDRS part 3 [7]. Briefly, the examiner instructed the patient to stand erect with eyes open and feet comfortably apart and parallel to each other. There was a solid wall at least 1 to 2 meters behind the examiner. The examiner informed the patient of testing process and explained that the patient was allowed to take a step backwards to avoid falling. First, the examiner then delivered a quick, forceful pull on the shoulders of the patient. The pull is purposely mild and not rated. Second, the shoulders were pulled briskly and forcefully towards the examiner. The pull test was performed approximately 10 minutes after the stimulation. All of the patients were completely aware and understood the proceedings, as confirmed by personal interviews. The score for item 12 of the revised UPDRS part 3 [7] was determined before and after GVS. The average anterior and lateral bending angles while the patient was standing with their eyes open for 30 s were measured as described previously [3]. For the postural evaluation, the patients were instructed to stand comfortably with their feet 10 cm apart and with their arms along their trunk. To evaluate the anterior and lateral bending angles, we captured the patients’ sagittal and frontal posture using two digital video cameras and conducted a frame-by-frame video analysis. The anterior and lateral bending angles were calculated as the angles formed between the line joining the marker positioned on the C7 spinous process and the midpoints of the right and left posterior superior iliac spine, and the vertical reference lines in the sagittal and frontal planes. The values were calculated every 30 frames and then averaged. The protocol of this study was approved by the Medical Ethics Committee of Nara Medical University and Kio University, and written informed consent was obtained from all subjects.

RESULTS

Postural instability retropulsion was evident both before and after sham stimulation in patient 1, 2, and 3. After true GVS, the frequency of the retropulsion decreased in patient 1, 2, and 3, and the score for item 12 of the revised UPDRS part 3 [7] at the time of the highest postural instability changed from 3 to 0 in patient 1, 3 to 1 in patient 2, and 3 to 0 in patient 3 (Supplementary Video in the online-only Data Supplement). Detailed clinical information on the patients is shown in Table 1. In the other 2 patients, the severity of postural instability was unchanged after true GVS. The average lateral bending angles in patients 1 and 2 did not decrease, and the average anterior bending angle in patient 3 was mildly decreased. The other 2 patients showed mildly decreased lateral bending angles.

Table 1.

Clinical features of 5 patients with Parkinson’s disease

DISCUSSION

Our three patients showed a reduction in postural instability after GVS. Patients with PD have processing abnormalities in sensorimotor integration and organization that affect postural stability [9]. Postural stability depends on the appropriate integration of not only visual and somatosensory input but also vestibular information [10]. In patients with PD, vestibular disorders have been reported [4,11]. Several studies have investigated the relationship between vestibular dysfunction and postural instability and found that vestibular dysfunction was unrelated to postural deficits in patients with mild or moderate PD [12]. However, patients with PD have an abnormal vestibulocolic reflex and an impaired vestibulo-ocular reflex, which suggests that vestibular dysfunction contributes to postural instability and gait disorders [10]. Yamamoto et al. [13] reported that axial motor function was improved after stimulation of vestibular nerves by GVS in patients with parkinsonism. The vestibular dysfunction was ipsilateral to the lateral trunk flexion with PD, and dysfunction of vestibular control related to posture might be responsible for postural instability in PD [4], but the severity of the lateral trunk flexion or camptocormia in our patients was apparently not reduced after GVS. The vestibular afferent fibers send axons to the cerebellar vermis via the vestibular nuclei [14,15], which exerts a strong effect on the turnover of dopamine in the caudate and nucleus accumbens through the ventral tegmental area [16,17]. GVS activates the vestibular afferents, and the vestibular nerves influence the basal ganglia and limbic system [16,17] via the cerebellar vermis [14,15]. Positron emission tomographic studies in humans have shown activation in the putamen in response to vestibular stimulation [18,19]. In addition, vestibular afferents project to the basal ganglia, and outputs from the basal ganglia are directed to the brain stem, including the pedunculopontine nucleus and spinal cord [20]. GVS may activate these extrapyramidal connections through the vestibular nerves, leading to increased axial motor function and improving postural instability.

One limitation of this study is that part 3 alone of the pull test of the revised UPDRS is not enough to objectively quantify the magnitude of improvement in postural instability because of its poor test-retest reliability. A second limitation was the small sample size.

The mechanism of postural instability is complex and not completely understood. In fact, although 3 patients did respond to GVS, the postural instability of 2 other patients did not respond. However, the positive responses of those 3 patients suggest that GVS might be a therapeutic option for postural instability.

Supplementary Materials

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