Bilateral Peripheral Vestibular Loss Research Articles

Vestibular Contributions to Primate Neck Postural Muscle Activity during Natural Motion.

To maintain stable posture of the head and body during our everyday activities, the brain integrates information across multiple sensory systems. Here, we examined how the primate vestibular system, independently and in combination with visual sensory input, contributes to the sensorimotor control of head posture across the range of dynamic motion experienced during daily life. We recorded activity of single motor units in the splenius capitis and sternocleidomastoid muscles in rhesus monkeys during yaw rotations spanning the physiological range of self-motion (up to 20 Hz) in darkness. Splenius capitis motor unit responses continued to increase with frequency up to 16 Hz in normal animals, and were strikingly absent following bilateral peripheral vestibular loss. To determine whether visual information modulated these vestibular-driven neck muscle responses, we experimentally controlled the correspondence between visual and vestibular cues of self-motion. Surprisingly, visual information did not influence motor unit responses in normal animals, nor did it substitute for absent vestibular feedback following bilateral peripheral vestibular loss. A comparison of muscle activity evoked by broadband versus sinusoidal head motion further revealed that low-frequency responses were attenuated when low- and high-frequency self-motion were experienced concurrently. Finally, we found that vestibular-evoked responses were enhanced by increased autonomic arousal, quantified via pupil size. Together, our findings directly establish the vestibular system's contribution to the sensorimotor control of head posture across the dynamic motion range experienced during everyday activities, as well as how vestibular, visual, and autonomic inputs are integrated for postural control.SIGNIFICANCE STATEMENT Our sensory systems enable us to maintain control of our posture and balance as we move through the world. Notably, the vestibular system senses motion of the head and sends motor commands, via vestibulospinal pathways, to axial and limb muscles to stabilize posture. By recording the activity of single motor units, here we show, for the first time, that the vestibular system contributes to the sensorimotor control of head posture across the dynamic motion range experienced during everyday activities. Our results further establish how vestibular, autonomic, and visual inputs are integrated for postural control. This information is essential for understanding both the mechanisms underlying the control of posture and balance, and the impact of the loss of sensory function.

Perioperative vestibular assessment and testing

Vestibular disorders can be difficult to accurately diagnose and manage. A careful history and focused physical examination are typically adequate to establish a diagnosis and initiate medical treatment. Vestibular testing is an important component of the work-up, but it is particularly essential for patients being considered for surgical intervention for a vestibular disorder, where the testing can be used to more definitively confirm a suspected diagnosis and to determine baseline vestibular organ function. In this article, we will first briefly review key components of the history and physical examination of patients with vestibular complaints. We will then discuss the most commonly used vestibular tests and their role in the preoperative assessment of patients undergoing vestibular surgery, including nystagmography, caloric testing, rotary chair testing, video head impulse testing, and vestibular evoked myogenic potential testing.

Functional Testing of Vestibulo-Spinal Contributions to Balance Control: Insights From Tracking Improvement Following Acute Bilateral Peripheral Vestibular Loss.

Background: A battery of stance and gait tasks can be used to quantify functional deficits and track improvement in balance control following peripheral vestibular loss. An improvement could be due to at least 3 processes: partial peripheral recovery of sensory responses eliciting canal or otolith driven vestibular reflexes; central compensation of vestibular reflex gains, including substitution of intact otolith responses for pathological canal responses; or sensory substitution of visual and proprioceptive inputs for vestibular contributions to balance control.Results: We describe the presumed action of all 3 processes observed for a case of sudden incapacitating acute bilateral peripheral loss probably due to vestibular neuritis. Otolith responses were largely unaffected. However, pathological decreases in all canal-driven vestibular ocular reflex (VOR) gains were observed. After 3 months of vestibular rehabilitation, balance control was normal but VOR gains remained low.Conclusions: This case illustrates the difficulty in predicting balance control improvements from tests of the 10 vestibular end organs and emphasizes the need to test balance control function directly in order to determine if balance control has improved and is normal again despite remaining vestibular sensory deficits. This case also illustrates that the presence of residual otolithic function may be crucial for balance control improvement in cases of bilateral vestibular hypofunction.

Update on Vestibulotoxicity: How can we Recognize and Prevent it

Drugs and other substances may cause irreversible damage to the inner ear. The term vestibulotoxicity refers to the toxic effect on the peripheral vestibular system and is usually caused by damage to the hair cells of the semicircular canals and otolithic organs. The devastating consequence of vestibulotoxicity is bilateral peripheral vestibular loss, including the phenomenon of oscillopsia. Parenterally administered streptomycin and gentamicin are the most common cause of vestibulotoxicity. There are few descriptions of other potentially vestibulotoxic drugs and substances, including cisplatin, solvents, organophosphate poisoning and others. Analysis of the literature shows weak evidence for true vestibulotoxicity. Unilateral vestibulotoxicity has been described after the use of ear drops containing gentamicin and, interestingly, also after parenteral use of gentamicin. We here present an updated review of vestibulotoxicity, and suggest the appropriate investigation for suspected unilateral and bilateral vestibular loss.

Causes and characteristics of horizontal positional nystagmus

Direction changing horizontal positional nystagmus can be observed in a variety of central and peripheral vestibular disorders. We tested sixty subjects with horizontal positional nystagmus and vertigo on the Epley Omniax(®) rotator. Monocular video recordings were performed with the right or left ear down, in the supine and prone positions. Nystagmus slow-phase velocity (SPV) was plotted as a function of time. Thirty-one subjects diagnosed with horizontal canalolithiasis had paroxysmal horizontal geotropic nystagmus with the affected ear down (onset 0.8 ± 1 s, range 0-4.9 s, duration 11.7-47.9 s, peak SPV 79 ± 67°/s). The SPV peaked at 5-20 s and declined to 0 by 60 s; at 40 s from onset, the average SPV was 1.8 % of the peak. Nine subjects diagnosed with cupulolithiasis had persistent apogeotropic horizontal nystagmus (onset 0.7 ± 1.4 s, range 0-4.3 s). Peak SPV was 54.2 ± 31.8°/s and 26.6 ± 12.2°/s with unaffected and affected ears down, respectively. At 40 s, the average SPV had decayed to only 81 % (unaffected ear down) and 65 % (affected ear down) of the peak. Twenty subjects were diagnosed with disorders other than benign positional vertigo (BPV) [vestibular migraine (VM), Ménière's Disease, vestibular schwannoma, unilateral or bilateral peripheral vestibular loss]. Subjects with VM (n = 13) had persistent geotropic or apogeotropic horizontal nystagmus. On average, at 40 s from nystagmus onset, the SPV was 61 % of the peak. Two patients with Ménière's Disease had persistent apogeotropic horizontal nystagmus; the peak SPV at 40 s ranged between 28.6 and 49.5 % of the peak. Symptomatic horizontal positional nystagmus can be observed in canalolithiasis, cupulolithiasis and diverse central and peripheral vestibulopathies; its temporal and intensity profile could be helpful in the separation of these entities.

The effect of prosthetic feedback on the strategies and synergies used by vestibular loss subjects to control stance

BackgroundThis study investigated changes in stance movement strategies and muscle synergies when bilateral peripheral vestibular loss (BVL) subjects are provided feedback of pelvis sway angle.MethodsSix BVL (all male) and 7 age-matched male healthy control (HC) subjects performed 3 stance tasks: standing feet hip width apart, eyes closed, on a firm and foam surface, and eyes open on foam. Pelvis and upper trunk movements were recorded in the roll and pitch planes. Surface EMG was recorded from pairs of antagonistic muscles at the lower leg, trunk and upper arm. Subjects were first assessed without feedback. Then, they received training with vibrotactile, auditory, and fall-warning visual feedback during stance tasks before being reassessed with feedback.ResultsFeedback reduced pelvis sway angle displacements to values of HCs for all tasks. Movement strategies were reduced in amplitude but not otherwise changed by feedback. These strategies were not different from those of HCs before or after use of feedback. Low frequency motion was in-phase and high frequency motion anti-phasic. Feedback reduced amplitudes of EMG, activity ratios (synergies) of antagonistic muscle pairs and slightly reduced baseline muscle activity.ConclusionsThis is the first study demonstrating how vestibular loss subjects achieve a reduction of sway during stance with prosthetic feedback. Unchanged movement strategies with reduced amplitudes are achieved with improved antagonistic muscle synergies. This study suggests that both body movement and muscle measures could be explored when choosing feedback variables, feedback location, and patient groups for prosthetic devices which reduce sway of those with a tendency to fall.

Coordination of the head with respect to the trunk, pelvis, and lower leg during quiet stance after vestibular loss

This study examined the relationship between head and trunk sway and between pelvis and leg sway during quiet stance in subjects with long-standing bilateral peripheral vestibular loss (BVLs) comparing these relationships to those of age-matched healthy controls (HCs). All subjects performed three different stance tasks: standing quietly on a firm or foam support surface, with eyes closed (ECF or eyes closed on normal) and on foam with eyes open. Data were recorded with four pairs of body-worn gyroscopes to measure roll and pitch angular velocities at the head, upper trunk, pelvis and lower-leg. These velocities were spectrally analysed and integrated for angle correlation analysis in three frequency bands: below 0.7Hz (low pass, LP), above 3 Hz (high pass, HP) and in between (band pass, BP). For both groups head motion was greater than trunk and pelvis motion except for BVL subjects (BVLs) under ECF conditions. BVLs had greater motion than HCs at all measurement locations for ECF conditions. Angle correlation analysis indicated that the head was almost "locked" to the trunk for BVLs over the LP and BP frequency bands. Head movements for both groups were relatively independent of the trunk in the HP band. Power spectral density ratios, and transfer functions showed a similar result - head relative to trunk movements were less up to 3 Hz in all tests for BVLs. The resonant frequency of head-on-trunk motion was shifted to a higher frequency for BVLs: from 3.2 to 4.3 Hz in pitch, 4.6 to 5.4 Hz in roll. Both groups show greater lower-leg than pelvis motion. These data indicate that during quiet stance BVLs change the characteristics of their head on shoulder motion, reducing relative motion of the head below 3 Hz and increasing head resonant frequency. Presumably these changes are accomplished with increased use of proprioceptive neck reflexes.

<p>Clinical features of benign paroxysmal positional vertigo in Western Turkey</p>

Background: It was the aim of this study to analyze the clinical manifestations, the incidence of each variant and the co-morbid conditions of benign paroxysmal positional vertigo (BPPV) as well as the response to treatment.
 Methods: One hundred and fifty-seven patients with BPPV were reviewed prospectively. An extensive neurotologic examination was performed. All patients were treated with an appropriate canalith repositioning maneuver (CRM).
 Results: In 138 patients, the posterior canal (PC) was involved, in 14 patients, the horizontal canal (HC), in 2 patients, the anterior canal (AC), and in 3 patients, both the PC and HC. A history of head trauma was identified in 17 patients. In 1 patient, sensorineural hearing loss on the affected side and, in another, bilateral peripheral vestibular loss was present. A history of migraine was reported in 21 cases. A resolution attributable to the first CRM was achieved in 132 patients.
 Conclusions: PC involvement was the most frequent type, constituting 87.9% of all BPPV cases. HC, AC and mixed canal types were relatively rare constituting 8.9, 1.3 and 1.9% of the cases, respectively. Response to the first CRM was recorded in 84.1%. Association with migraine was recorded in 13.4% of the patients.
 Published courtesy of:Eur Neurol. 2008; 59(6): 315-319

Clinical Features of Benign Paroxysmal Positional Vertigo in Western Turkey

Background: It was the aim of this study to analyze the clinical manifestations, the incidence of each variant and the comorbid conditions of benign paroxysmal positional vertigo (BPPV) as well as the response to treatment. Methods: One hundred and fifty-seven patients with BPPV were reviewed prospectively. An extensive neurotologic examination was performed. All patients were treated with an appropriate canalith repositioning maneuver (CRM). Results: In 138 patients, the posterior canal (PC) was involved, in 14 patients, the horizontal canal (HC), in 2 patients, the anterior canal (AC), and in 3 patients, both the PC and HC. A history of head trauma was identified in 17 patients. In 1 patient sensorineural hearing loss on the affected side and in another bilateral peripheral vestibular loss was present. A history of migraine was reported in 21 cases. A resolution attributable to the first CRM was achieved in 132 patients. Conclusions: PC involvement was the most frequent type constituting 87.9% of all BPPV cases. HC, AC and mixed canal types were relatively rare constituting 8.9, 1.3 and 1.9% of the cases, respectively. Response to the first CRM was recorded in 84.1%. Association with migraine was recorded in 13.4% of the patients.

The balance control of bilateral peripheral vestibular loss subjects and its improvement with auditory prosthetic feedback

We investigated whether long-term bilateral vestibular loss subjects could combine auditory biofeedback of trunk sway with their remaining natural sensory inputs on balance to provide an improved control of trunk sway. A successful integration of natural and artificial signals would provide a basis for a balance prosthesis. Trunk sway of 6 bilateral peripheral vestibular loss subjects (BVL) was recorded using either angular position- or velocity-based auditory feedback or no feedback during stance and gait tasks. Roll and pitch trunk movements were recorded with angular velocity transducers mounted just above the waist and feedback without a delay to 4 loudspeakers placed at the left, right, front and rear borders of the 5 m long by 4 m wide test environment. The two types of auditory feedback or no feedback were provided to the subjects in random order. In the feedback modes, sway greater than a preset angle (ca. 0.5 deg) or velocity (ca. 3 deg/s) thresholds caused a tone to be emitted from the speaker towards which the subject moved. The tone volume increased with increasing angle or angular velocity amplitude. For all stance tasks BVL subjects without auditory feedback had a significantly different balance control with respect to that of normal controls. BVL sway values eyes open on a normal surface were reduced with auditory feedback with the greatest reductions in the roll plane. Specifically for the task of standing on 1 leg eyes open with position-auditory- feedback, amplitudes of pitch and roll angles and angular velocities were indistinguishable from those of normal controls. Sway during stance tasks on foam with eyes closed showed no improvement with feedback, remaining greater than normal. For some gait tasks there was a decrease in trunk sway with velocity feedback. These initial results indicate that subjects with vestibular loss could incorporate the auditory prosthetic sensory information into their balance commands, particularly in the roll plane if the balance task is performed with eyes open. Position information appears more useful than velocity information in reducing trunk sway during stance tasks. Future work will need to determine the effect of a training time on the improvement in balance control using such a prosthetic device and the ideal position and velocity auditory feedback combination.

Differential diagnosis of proprioceptive and vestibular deficits using dynamic support-surface posturography.

The objective of this study was to evaluate how effective dynamic support-surface posturography could be as a diagnostic tool in patients with balance disorders (proprioceptive or vestibular deficits). Specifically, we studied whether measures of trunk control and simple toe-up rotational perturbations, selected using statistical techniques, could provide a better diagnostic yield than either the analysis of lower-body movements or use of a "nulled" ankle input paradigm. The test subjects were 15 control subjects, five patients with bilateral peripheral vestibular loss (VL) and five patients with selective bilateral, lower-leg proprioceptive loss (PL). Amplitudes and onset latencies of bursts of EMG activity in upper and lower-leg muscles, paraspinals and trapezius muscles, concurrent changes in ankle torque, and peak amplitudes of upper-leg, lower-leg, and trunk angular-velocities were measured. Stimuli included three different types of sudden movements of the support surface, a "nulled" ankle input paradigm, a simple toe-up rotation paradigm, and a combined toe-up rotation and backwards translation of the support surface. All stimuli were tested under eyes-open and eyes-closed conditions. For each type of movement and condition the diagnostic classification accuracy (i.e. the overall sensitivity and specificity) was calculated based on those posturography measures providing the highest diagnostic separation between the three populations. Both patient groups showed increased trunk sway, changed support-surface reaction forces and muscle amplitudes compared with controls for toe-up and "nulled" test conditions. Measures providing the greatest diagnostic utility were the amplitude of trunk-angular velocity (increased in VL subjects, less so in PL), the amplitude of balance-correcting paraspinal responses (increased in VL subjects, decreased in PL subjects), the amplitude of trapezius stabilising responses (increased in both patient groups) for simple toe-up rotations under eyes-closed conditions. We conclude, that diagnosis of balance disorders using dynamic posturography is best achieved using measures of trunk control following pure toe-up rotational perturbations tested under eyes-closed conditions.

Vestibular influences on human postural control in combinations of pitch and roll planes reveal differences in spatiotemporal processing

The present study examined the influence of bilateral peripheral vestibular loss (BVL) in humans on postural responses to multidirectional surface rotations in the pitch and roll planes. Specifically, we examined the effects of vestibular loss on the directional sensitivity, timing, and amplitude of early stretch, balance correcting, and stabilizing reactions in postural leg and trunk muscles as well as changes in ankle torque and trunk angular velocity following multidirectional rotational perturbations of the support surface. Fourteen normal healthy adults and five BVL patients stood on a dual axis rotating platform which rotated 7.5 degrees at 50 degrees/s through eight different directions of pitch and roll combinations separated by 45 degrees. Directions were randomized within a series of 44 perturbation trials which were presented first with eyes open, followed by a second series of trials with eyes closed. Vestibular loss did not influence the range of activation or direction of maximum sensitivity for balance correcting responses (120-220 ms). Response onsets at approximately 120 ms were normal in tibialis anterior (TA), soleus (SOL), paraspinals (PARAS), or quadriceps muscles. Only SOL muscle activity demonstrated a 38- to 45-ms delay for combinations of forward (toe-down) and roll perturbations in BVL patients. The amplitude of balance correcting responses in leg muscles between 120 and 220 ms was, with one exception, severely reduced in BVL patients for eyes open and eyes closed conditions. SOL responses were decreased bilaterally for toe-up and toe-down perturbations, but more significantly reduced in the downhill (load-bearing) leg for combined roll and pitch perturbations. TA was significantly reduced bilaterally for toe-up perturbations, and in the downhill leg for backward roll perturbations. Forward perturbations, however, elicited significantly larger TA activity in BVL between 120 and 220 ms compared to normals, which would act to further destabilize the body. As a result of these changes in response amplitudes, BVL patients had reduced balance correcting ankle torque between 160 and 260 ms and increased torque between 280 and 380 ms compared to normals. There were no differences in the orientation of the resultant ankle torque vectors between BVL and normals, both of which were oriented primarily along the pitch plane. For combinations of backward (toe-up) and roll perturbations BVL patients had larger balance correcting and stabilizing reactions (between 350 and 700 ms) in PARAS than normals and these corresponded to excessive trunk pitch and roll velocities. During roll perturbations, trunk velocities in BVL subjects after 200 ms were directed along directions different from those of normals. Furthermore, roll instabilities appeared later than those of pitch particularly for backward roll perturbations. The results of the study show that combinations of roll and pitch surface rotations yield important spatiotemporal information, especially with respect to trunk response strategies changed by BVL which are not revealed by pitch plane perturbations alone. Our results indicate that vestibular influences are earlier for the pitch plane and are directed to leg muscles, whereas roll control is later and focused on trunk muscles.

Interactions between vestibular and proprioceptive inputs triggering and modulating human balance-correcting responses differ across muscles.

Interactions between proprioceptive and vestibular inputs contributing to the generation of balance corrections may vary across muscles depending on the availability of sensory information at centres initiating and modulating muscle synergies, and the efficacy with which the muscle action can prevent a fall. Information which is not available from one sensory system may be obtained by switching to another. Alternatively, interactions between sensory systems and the muscle to which this interaction is targeted may be fixed during neural development and not switchable. To investigate these different concepts, balance corrections with three different sets of proprioceptive trigger signals were examined under eyes-open and eyes-closed conditions in the muscles of normal subjects and compared with those of subjects with bilateral peripheral vestibular loss. The different sets of early proprioceptive inputs were obtained by employing three combinations of support surface rotation and translation, for which ankle inputs were nulled, normal or enhanced, the knees were either locked or in flexion, and the trunk was either in flexion or extension. Three types of proprioceptive and vestibulospinal interactions were identified in muscles responses. These interactions were typified by the responses of triceps surae, quadriceps, and paraspinal muscles. The amplitudes of stretch responses at 50 ms after the onset of ankle flexion in triceps surae muscles were related to the velocity of ankle stretch. The amplitude of balance-correcting responses at 100 ms corresponded more with stretch of the biarticular gastrocnemius when the knee was re-extended at 60 ms. Absent stretch reflexes at 50 ms in triceps surae with nulled ankle inputs caused a minor, 12-ms delay in the onset of balance-correcting responses in triceps surae muscles. Vestibular loss caused no change in the amplitude of balance-correcting responses, but a negligible decrease in onset latency in triceps surae even with nulled ankle inputs. Stretch responses in quadriceps at 80 ms increased with the velocity of knee flexion but were overall lower in amplitude in vestibular loss subjects. Balance-correcting responses in quadriceps had amplitudes which were related to the directions of initial trunk movements, were still present when knee inputs were negligible and were also altered after vestibular loss. Stretch and unloading responses in paraspinals at 80 ms were consistent with the direction of initial trunk flexion and extension. Subsequent balance-correcting responses in paraspinals were delayed 20 ms in onset and altered in amplitude by vestibular loss. The changes in the amplitudes of ankle (tibialis anterior), knee (quadriceps) and trunk (paraspinal) muscle responses with vestibular loss affected the amplitudes and timing of trunk angular velocities, requiring increased stabilizing tibialis anterior, paraspinal and trapezius responses post 240 ms as these subjects attempted to remain upright. The results suggest that trunk inputs provide an ideal candidate for triggering balance corrections as these would still be present when vestibular, ankle and knee inputs are absent. The disparity between the amplitudes of stretch reflex and automatic balance-correcting responses in triceps surae and the insignificant alteration in the timing of balance-correcting responses in these muscles with nulled ankle inputs indicates that ankle inputs do not trigger balance corrections. Furthermore, modulation of balance corrections normally performed by vestibular inputs in some but not all muscles is not achieved by switching to another sensory system on vestibular loss. We postulate that a confluence of trunk and upper-leg proprioceptive input establishes the basic timing of automatic, triggered balance corrections which is then preferentially weighted by vestibular modulation in muscles that prevent falling. (ABSTRACT TRUNCATED)

Physical Therapy Management of a Patient With Bilateral Peripheral Vestibular Loss

Physical Therapy Management of a Patient With Bilateral Peripheral Vestibular Loss: A Case Report: PDF Only

The horizontal vestibulo‐ocular reflex gain during active and passive high‐frequency head movements

Patients with bilateral peripheral vestibular loss complain of varying degrees of oscillopsia and balance difficulties. Some are able to engage in sporting activities while others are completely disabled. An assumption that other inputs are available to the vestibulo-ocular reflex (VOR) enabling it to achieve some degree of visual stability during high-frequency head movement is reasonable. In this study, the gain of the horizontal vestibulo-ocular reflex in 10 healthy subjects was examined during active high-frequency head-on-body rotation (head free), and compared to high-frequency passive whole-body rotation (head fixed). A statistical difference in the gain (P < .002) was noted for all frequencies between the two groups. In those individuals undergoing passive whole-body high-frequency movements, the gain was observed to rise (above unity) with increasing frequency of rotation, while the gain during active head-on-body rotation remained close to 1.