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DOI: 10.1055/s-0040-1722174
Cervical Vestibular-Evoked Myogenic Potentials and Balance Testing in Children with Down Syndrome
Abstract
Introduction Vestibular otolith function plays a major role in balance control.
Objective To investigate the saccular and balance functions of children with Down syndrome (DS).
Methods In total, 15 children with DS aged between 9 and 11 years were included. An age- and gender-matched control group (CG) composed of 15 normal participants was also included. The subjects with DS had trisomy 21, without hearing or organic problems, and they had independence in stance. The saccular function among the children with DS and among the controls was tested using air-conduction cervical vestibular-evoked myogenic potentials (cVEMPs). In addition, the static and dynamic balance statuses were evaluated using the following assessments; the Pediatric Balance Scale (PBS), the modified Clinical Test of Sensory Interaction on Balance (mCTSIB), the Romberg test, and the Timed Up and Go (TUG) test.
Results In the present study, the results of the saccular function test showed that there was a significant difference between children with and without DS (p < 0.05). The DS subjects had significantly earlier N1 latancy and lower amplitude of the cVEMPs (< 70 μV) compared with the control subjects. The static-dynamic balance ability was statistically and significantly different in children with DS compared with the controls (p < 0.05).
Conclusion These results revealed that saccular function seems to be affected in DS subjects. The dysfunction in static and dynamic balance abilities of the children with DS may be attributed to vestibular dysfunction as well as low gross motor skills. This knowledge should be taken into account when assessing motor performance in those subjects. Additional larger studies testing other dimensions of the vestibular system in children with DS are needed.
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Introduction
Down syndrome (DS) is one of the most common chromosomal birth defects in children,[1] and it is the phenotypic consequence of trisomy 21. As consequence of nonhereditary intellectual disability, several problems arise, such as developmental delay, respiratory dysfunctions, vision problems, hearing problems, and balance dysfunction.[2] [3] Control of balance requires the integration of vestibular sensory information with somatosensory and visual information,[4] and its dysfunction may be evaluated via standardized scales and tests. Some of those are the Pediatric Balance Scale (PBS),[4] the Romberg test,[5] the Modified Clinical Test of Sensory Interaction on Balance (mCTSIB),[6] and the Timed Up and Go (TUG) test.[7] These tests and their uses are presented in [Table 1].
Pediatric Balance Scale (PBS) |
Functional balance in everyday life activities (Franjoine et al.,[4] 2003). |
Romberg test |
The integrity among different sensory organs and neuronal conduction pathways utilized in the constitution of balance (Black et al.,[5] 1982). |
Modified Clinical Test of Sensory Interaction on Balance (mCTSIB) |
Sensory system dysfunction on a stable and unstable floor, with eyes open and closed. In the tests on unstable ground with the eyes closed, the effects of visual and somatosensory inputs are eliminated, and the effects of vestibular inputs on postural stability are evaluated more efficiently (Shumway-Cook et al.,[6] 1986). |
Timed Up and Go Test (TUG) |
Functional mobility and balance through different variables such as walking speed, postural control, functional mobility, and balance are evaluated (Podsiadlo et al.,7 1991). |
The vestibular system is responsible for maintaining the sense of head orientation and acceleration, both at rest and in motion.[8] [9] Vestibular inputs through vestibulo-spinal connections play a major role in trunk stabilization.[10] The activation of otolith organs evokes the vestibulocollic reflex (VCR), which provides stabilization of the position of the head in space.[11] The cervical vestibular evoked myogenic potential (cVEMP) is a test used for neurotologic examination both in adults and in children. It verifies the integrity of vestibular otolith function through a muscular response evoked by a high-intensity acoustic stimulation which activates the saccular macula and records the transient inhibition of the sternocleidomastoid (SCM) muscle via surface electrodes.
While several studies have reported balance and gait dysfunction in DS,[12] [13] [14] the impact of vestibular otolith function in balance control in DS has not been fully addressed. The principal aim of the present study was to assess vestibular otolith function using cervical vestibular-evoked myogenic potentials (cVEMPs) in children with DS and matched control children. In addition, the static and dynamic balance performances were also measured through conventional balance tests and correlated with cVEMP responses.
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Methods
The present study was conducted in compliance with the Declaration of Helsinki, and it was approved by the local Ethics in Research Committee. In total, 15 children with DS, 7 females and 8 males, aged between 9 and 11 years (mean age: 10.25 ± 0.70 years) were included. An age- and gender-matched control group (CG) composed of 15 participants (7 females and 8 males) without DS was also included. The inclusion criteria for the subjects in the DS group were: the presence of trisomy 21; the absence of any visual or organic disorders, and independence in stance and ambulation (having no hearing loss, no additional impairment, and no neurologic or vestibular system problem). The participants in the control group were healthy, with no orthopedic or neurological disorders, no impairment in somatosensory activity, hearing, vestibular or uncorrected visual functions, and free of medications for at least three months before the beginning of the study. Written informed consent was obtained from all parents and children.
All children (DS and control) underwent the cVEMP, the PBS, the Romberg test, the mCTSIB and the TUG test. The CVEMPs were recorded with the Neurosoft Neuro-Audio.Net (Neurosoft Ltd., Ivanovo, Russia) software. The electromyographic activity of the SCM muscle was recorded while the children were sitting on a chair and were asked to turn their head to both sides to activate their neck flexors, and the saccular receptors were acoustically stimulated. Electromyography (EMG) biofeedback was used to reject all traces outside the minimum/maximum root mean square (RMS) EMG limits. Prior to the cVEMP test, the maximum contraction level is determined for each individual. Then, the target level for all subsequent cVEMP tests is set at ∼ 70% to 80% of the maximum contraction level. The RMS is calculated for the EMG before each stimulus (prestimulus area) and displayed on a dial on a computer screen for the patient to see. The subjects are instructed to keep the EMG level constant and at a predefined target level (50 μV ± 20 μV). The acoustic stimulus was a click of 500 Hz at an intensity of 105 dB nHL. The rate was of 4 stimuli per second, and it was presented monoaurally through earphones. Recordings were obtained with an average of 200 stimuli response, and 2 traces from each side were obtained to assess reproducibility. In each trace, we determined the latency of positive-negative waves (P1 and N1), in addition to the amplitude of the P1-N1.
Functional balance in everyday activities is measured with PBS on a 5-point scale to obtain overall scores for each subject. In the Romberg test, children were asked to stand upwards for 30 seconds withtheir eyes closed, and then we noted whether they could sustain their position or not. In the mCTSIB, children were asked to preserve their balance in 4 different conditions (eyes open, on stable ground; eyes closed, on stable ground; eyes open, on unstable ground; and eyes closed, on unstable ground), and the maximum time each child managed to stand in balance was recorded. In the TUG test, the participants were seated on a chair and asked to stand up without handling the grip, and to walk 3 m and take a seat again. The time to complete the task was recorded. All tests were conducted in the same day, with adequate breaks between them.
The variables studied were: gender; date of birth; latency to onset of the P1 wave; latency to onset of the N1 wave; value of the P1-N2 amplitude. Overall scores for the scale and the time (seconds) for the other tests were recorded. Descriptive data were expressed as means and standard deviations. In addition, the measurements of the central tendency (median) of the continuous variables were calculated, as well as their respective interquartile range (IQR). For the comparative analyses concerning cVEMP responses (latencies and amplitudes) and balance tests between patient and control groups and also in relation to gender, the Mann-Whitney U test was used. Values of p < 0.05 indicated statistical significance.
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Results
The demographics of the subjects in both groups are presented in [Table 2]. There were no significant differences regarding age and gender between the two groups (p > 0.05). To assess saccular function and differentiate from healthy controls (30 ears of 15 children), the air-conduction cVEMP test was administered to 30 ears of 15 children with DS; in addition, the severity if the balance dysfunction was evaluated with PBS, the Romberg test, the mCTSIB and the TUG test.
Testing of the cVEMPs was performed on both sides in all DS and control subjects. All subjects (100%) completed the cVEMP testing with data for analysis. In total, 30 (60%) subjects included for analysis had measurable bilateral responses at 105 dB of air-conducted click stimulus. The P1 and N1 peak latencies for the DS subjects ranged from 10.80 ms to 13.40 ms, with a median (IQR) of 12.40 ms (1.00 ms), and from 16.00 ms to 20.40 ms, with a median of 18.30 ms (1.70 ms) respectively. The P1-N1 amplitudes for the DS group ranged from 33.30 μV to 83.50 μV, with a median amplitude (IQR) of 62.30 μV (19.75 μV). The P1 and N1 peak latencies for the control subjects ranged from 11.40 ms to 18.50 ms, with a median (IQR) of 12.70 ms (1.10 ms), and from 17.30 ms to 26.20 ms, with a median (IQR) of 20.00 ms (2.30 ms) respectively. The P1-N1 amplitudes for the control group ranged from 36.40 μV to 174.70 μV, with a median (IQR) of 104.75 μV (59.05 μV). [Table 3] shows the median values (IQR) of the P1, N1 latancies and the amplitude of the P1-N1 obtained for the whole sample.
The statistical analysis demonstrated a significant difference between DS and control subjects in the latencies of N1 (p = 0.000) and the amplitude of P1-N1 (p = 000). There was no significant difference among cVEMP parameters regarding the right and the left ears of the control subjects or regarding gender (p > 0.05).
The ability of the subjects to maintain a quiet upright stance was assessed with the mCTSIB under four conditions in which sensory inputs were systematically altered. Balance times were recorded. All subjects in both groups were able to fully maintain their balance for 30 seconds. The Romberg test was negative for the whole sample, which means that all subjects could stand with their eyes closed for 30 seconds. The median PBS score (IQR) for the DS subjects was of 30.00 s (7.00 s), which was significantly lower than that of the control subjects (56.00 s [0.00 s]; p = 000). Task in the TUG test for DS 20.00 (8.00) which significantly longer than control subjects 9.00 (1.00) (p = 000).
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Discussion
In the present study, the results of the saccular function test showed that there was a significant difference between children with and without DS. The DS subjects had significantly earlier N1 latancy and lower amplitude in the cVEMPs (< 70m V) compared with the control subjects. In addition, there was a statistically significant difference in the static-dynamic balance ability in DS children compared with the controls.
Under everyday conditions, the vestibular system works in a complementary way with the somatosensory and visual systems to provide balance/postural control. Balance functions of DS has been put forth before,[12] [13] [14] [15] and the cVEMPs have been extensively studied in subjects without DS,[16] [17] [18] [19] as well as some other pathological conditions.[20] On the contrary, balance function and cVEMP testing have not been correlated in DS before.
The present study was performed to compare balance and saccular functions between DS children and typically developing children. In this regard, the static balance and the dynamic balance were tested and correlated with the saccular function test (cVEMP). As expected, the DS children had significant differences in all areas of balance ability in comparison with typically developing children (p < 0.05). Typically developing children showed higher balance ability than the DS children. This is in line with the following previous study results: the static-dynamic balance of DS children showed more differences compared with typically developing children and DS children lack static balance ability.[12] [14] [15] The reason for this is that their muscle reaction velocity is significantly slower compared with their peers,[21] and there is much difficulty with motor control.
We used the cVEMP with air-conduction stimuli that measures saccular function. The cVEMPs were recorded while the children were sitting on a chair and were asked to turn their head to both sides to activate their neck flexors bilaterally. As mentioned in the literature,[16] activation of the the SCM muscle by turning the head while sitting was sufficient to generate the cVEMP responses without early fatigue. Reproducible, unrectified cVEMP tracings were easily obtained with clicks at 105 dB in all DS and control children. In other words, the response rate in the present study was of 100%. Despite the usual muscle weakness and motor control handicap among DS children, the cVEMPs could be easily recorded in those subjects.
Our results demonstrated that the cVEMP parameters for the control group are similar to the normative values, as reported in the literature.[18] On the other hand, we detected that the fundamental parameters of the cVEMP test (latency and amplitude) among DS children are significantly different than those obtained among the controls. Differences in latencies and amplitudes should be considered as N1 latencies were shorter and P1-N1 amplitudes were lower than those obtained among the controls. These results suggest that cVEMPs recording, demonstrating that the saccule, the vestibular afferent fibers and the vestibular nuclei are not similar to tupically developing children. No statistically significant difference was detected between the right and left sides regarding the P1 and N1 latencies and the P1-N1 amplitude. This agrees with the studies by Picciotti et al.[17] and Gonzalez et al.,[22] who demonstrated no differences between the right and left ears.
The recording rate was of 100%. This means that the cVEMP test could be applied successfully to diagnose saccular function among the pediatric DS population, as it can be recorded easily in all children to make appropriate decisions about interventions and program placement and planning, and to track the progress of children with DS.
Regarding the use of cVEMPs in the examination of the vestibular system in the pediatric population, Tribukait et al.[23] showed that the function of the semicircular canal correlated best with the function of the saccule, and, if the hearing was better than 90 dB, the function of the vestibular otolith was often normal, while for hearing levels of 100 dB to 120 dB, otolith function declined significantly. De Kegel et al.[24] found that children between 3 and 12 years of age with moderate hearing impairment and absent cVEMP perform significantly weaker on static balance measurements in which visual and/or somatosensory information is unreliable. This confirms that the saccule has an important role in the development of static balance.
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Conclusion
In the present study, the most remarkable result is that cVEMP responses are effected in children with DS means that saccular function is altered in those children. This finding may have implications to the understanding of the basis of the balance problem that affects children with DS in their everyday lives. When assessing static and dynamic balance dysfuction among DS children, vestibular otolith functions should be considered. Future studies on the functions of the utricle and semicircular canal are needed for a more complete understanding of vestibular dysfunction among DS children.
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Conflict of Interests
The authors have no conflict of interests to declare.
Availability of Data and Material
The datasets used during the current study may be made available by the corresponding author upon reasonable request.
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References
- 1 Presson AP, Partyka G, Jensen KM. et al. Current estimate of Down Syndrome population prevalence in the United States. J Pediatr 2013; 163 (04) 1163-1168
- 2 Roizen NJ, Magyar CI, Kuschner ES. et al. A community cross-sectional survey of medical problems in 440 children with Down syndrome in New York State. J Pediatr 2014; 164 (04) 871-875
- 3 Chen HL, Yeh CF, Howe TH. Postural control during standing reach in children with Down syndrome. Res Dev Disabil 2015; 38: 345-351
- 4 Franjoine MR, Gunther JS, Taylor MJ. Pediatric balance scale: a modified version of the berg balance scale for the school-age child with mild to moderate motor impairment. Pediatr Phys Ther 2003; 15 (02) 114-128
- 5 Black FO, Wall III C, Rockette Jr HE, Kitch R. Normal subject postural sway during the Romberg test. Am J Otolaryngol 1982; 3 (05) 309-318
- 6 Shumway-Cook A, Horak FB. Assessing the influence of sensory interaction of balance. Suggestion from the field. Phys Ther 1986; 66 (10) 1548-1550
- 7 Podsiadlo D, Richardson S. The timed “Up & Go”: a test of basic functional mobility for frail elderly persons. J Am Geriatr Soc 1991; 39 (02) 142-148
- 8 Horak FB, Shupert CL, Dietz V, Horstmann G. Vestibular and somatosensory contributions to responses to head and body displacements in stance. Exp Brain Res 1994; 100 (01) 93-106
- 9 Goldberg JM. The vestibular system: a sixth sense. Oxford; New York: Oxford University Press; 2012
- 10 Layman AJ, Li C, Carey JP. et al. Influence of age-related loss of otolith function on gait: Data from the baltimore longitudinal study on aging. Otol Neurotol 2015; 36 (02) 260-266
- 11 Wilson VJ, Boyle R, Fukushima K. et al. The vestibulocollic reflex. J Vestib Res 1995; 5 (03) 147-170
- 12 Rigoldi C, Galli M, Mainardi L, Crivellini M, Albertini G. Postural control in children, teenagers and adults with Down syndrome. Res Dev Disabil 2011; 32 (01) 170-175
- 13 Gomes MM, Barela JA. Postural control in down syndrome: the use of somatosensory and visual information to attenuate body sway. Mot Contr 2007; 11 (03) 224-234
- 14 Galli M, Rigoldi C, Mainardi L, Tenore N, Onorati P, Albertini G. Postural control in patients with Down syndrome. Disabil Rehabil 2008; 30 (17) 1274-1278
- 15 Vuillerme N, Marin L, Debu B. Assessment of static postural control in teenagers with Down syndrome. Adapt Phys Activ Q 2001; 18 (04) 417-433
- 16 Isaradisaikul S, Navacharoen N, Hanprasertpong C, Kangsanarak J. Cervical vestibular-evoked myogenic potentials: norms and protocols. Int J Otolaryngol 2012; 2012: 913515
- 17 Picciotti PM, Fiorita A, Di Nardo W, Calò L, Scarano E, Paludetti G. Vestibular evoked myogenic potentials in children. Int J Pediatr Otorhinolaryngol 2007; 71 (01) 29-33
- 18 Kelsch TA, Schaefer LA, Esquivel CR. Vestibular evoked myogenic potentials in young children: test parameters and normative data. Laryngoscope 2006; 116 (06) 895-900
- 19 Sheykholeslami K, Megerian CA, Arnold JE, Kaga K. Vestibular-evoked myogenic potentials in infancy and early childhood. Laryngoscope 2005; 115 (08) 1440-1444
- 20 Murofushi T. Clinical application of vestibular evoked myogenic potential (VEMP). Auris Nasus Larynx 2016; 43 (04) 367-376
- 21 Chang CL, Kubo M, Ulrich BD. Emergence of neuromuscular patterns during walking in toddlers with typical development and with Down syndrome. Hum Mov Sci 2009; 28 (02) 283-296
- 22 Gonzalez E, Piqeras M, Martin V. et al. [The vestibulocollic reflex: assessment and characteristics of vestibular-evoked myogenic potentials analysed by age groups]. Rev Neurol 2007; 44 (06) 339-442
- 23 Tribukait A, Brantberg K, Bergenius J. Function of semicircular canals, utricles and saccules in deaf children. Acta Otolaryngol 2004; 124 (01) 41-48
- 24 De Kegel A, Maes L, Baetens T, Dhooge I, Van Waelvelde H. The influence of a vestibular dysfunction on the motor development of hearing-impaired children. Laryngoscope 2012; 122 (12) 2837-2843
Address for correspondence
Publikationsverlauf
Eingereicht: 27. August 2020
Angenommen: 08. November 2020
Artikel online veröffentlicht:
19. Februar 2021
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References
- 1 Presson AP, Partyka G, Jensen KM. et al. Current estimate of Down Syndrome population prevalence in the United States. J Pediatr 2013; 163 (04) 1163-1168
- 2 Roizen NJ, Magyar CI, Kuschner ES. et al. A community cross-sectional survey of medical problems in 440 children with Down syndrome in New York State. J Pediatr 2014; 164 (04) 871-875
- 3 Chen HL, Yeh CF, Howe TH. Postural control during standing reach in children with Down syndrome. Res Dev Disabil 2015; 38: 345-351
- 4 Franjoine MR, Gunther JS, Taylor MJ. Pediatric balance scale: a modified version of the berg balance scale for the school-age child with mild to moderate motor impairment. Pediatr Phys Ther 2003; 15 (02) 114-128
- 5 Black FO, Wall III C, Rockette Jr HE, Kitch R. Normal subject postural sway during the Romberg test. Am J Otolaryngol 1982; 3 (05) 309-318
- 6 Shumway-Cook A, Horak FB. Assessing the influence of sensory interaction of balance. Suggestion from the field. Phys Ther 1986; 66 (10) 1548-1550
- 7 Podsiadlo D, Richardson S. The timed “Up & Go”: a test of basic functional mobility for frail elderly persons. J Am Geriatr Soc 1991; 39 (02) 142-148
- 8 Horak FB, Shupert CL, Dietz V, Horstmann G. Vestibular and somatosensory contributions to responses to head and body displacements in stance. Exp Brain Res 1994; 100 (01) 93-106
- 9 Goldberg JM. The vestibular system: a sixth sense. Oxford; New York: Oxford University Press; 2012
- 10 Layman AJ, Li C, Carey JP. et al. Influence of age-related loss of otolith function on gait: Data from the baltimore longitudinal study on aging. Otol Neurotol 2015; 36 (02) 260-266
- 11 Wilson VJ, Boyle R, Fukushima K. et al. The vestibulocollic reflex. J Vestib Res 1995; 5 (03) 147-170
- 12 Rigoldi C, Galli M, Mainardi L, Crivellini M, Albertini G. Postural control in children, teenagers and adults with Down syndrome. Res Dev Disabil 2011; 32 (01) 170-175
- 13 Gomes MM, Barela JA. Postural control in down syndrome: the use of somatosensory and visual information to attenuate body sway. Mot Contr 2007; 11 (03) 224-234
- 14 Galli M, Rigoldi C, Mainardi L, Tenore N, Onorati P, Albertini G. Postural control in patients with Down syndrome. Disabil Rehabil 2008; 30 (17) 1274-1278
- 15 Vuillerme N, Marin L, Debu B. Assessment of static postural control in teenagers with Down syndrome. Adapt Phys Activ Q 2001; 18 (04) 417-433
- 16 Isaradisaikul S, Navacharoen N, Hanprasertpong C, Kangsanarak J. Cervical vestibular-evoked myogenic potentials: norms and protocols. Int J Otolaryngol 2012; 2012: 913515
- 17 Picciotti PM, Fiorita A, Di Nardo W, Calò L, Scarano E, Paludetti G. Vestibular evoked myogenic potentials in children. Int J Pediatr Otorhinolaryngol 2007; 71 (01) 29-33
- 18 Kelsch TA, Schaefer LA, Esquivel CR. Vestibular evoked myogenic potentials in young children: test parameters and normative data. Laryngoscope 2006; 116 (06) 895-900
- 19 Sheykholeslami K, Megerian CA, Arnold JE, Kaga K. Vestibular-evoked myogenic potentials in infancy and early childhood. Laryngoscope 2005; 115 (08) 1440-1444
- 20 Murofushi T. Clinical application of vestibular evoked myogenic potential (VEMP). Auris Nasus Larynx 2016; 43 (04) 367-376
- 21 Chang CL, Kubo M, Ulrich BD. Emergence of neuromuscular patterns during walking in toddlers with typical development and with Down syndrome. Hum Mov Sci 2009; 28 (02) 283-296
- 22 Gonzalez E, Piqeras M, Martin V. et al. [The vestibulocollic reflex: assessment and characteristics of vestibular-evoked myogenic potentials analysed by age groups]. Rev Neurol 2007; 44 (06) 339-442
- 23 Tribukait A, Brantberg K, Bergenius J. Function of semicircular canals, utricles and saccules in deaf children. Acta Otolaryngol 2004; 124 (01) 41-48
- 24 De Kegel A, Maes L, Baetens T, Dhooge I, Van Waelvelde H. The influence of a vestibular dysfunction on the motor development of hearing-impaired children. Laryngoscope 2012; 122 (12) 2837-2843