Vestibular dysfunction is caused by pathologies in the peripheral and central vestibular system. The peripheral pathologies constitute 90% of cases with vertigo. ¹ It involves lesion in the end organs of the inner ear and/or the eighth cranial nerve. The central vestibular pathologies involve lesion in the cortical and sub-cortical pathways of the vestibular system. Vestibular dysfunction results in several adverse physical outcomes such as postural instability, abnormal gait and falls. Further, the majority of individuals with vestibular dysfunction are also found to have anxiety and depression. ² In addition, the loss of vestibular sensory information is shown to alter cognitive abilities related to the processing of spatial and non-spatial information. ³

Several studies have investigated the cognitive abilities of individuals with vestibular dysfunction. According to literature, parabrachial nucleus and the hippocampus are the anatomically two regions that account for the relation between the vestibular system and neural networks involved in cognitive and emotional processing. ⁴ The different cognitive skills associated with vestibular function include attention, visuospatial orientation, executive function, memory, metacognition, and self-control. ⁵ Research on cognition assessment pertaining to vestibular function has mainly been based on spatial orientation, attention, memory, and executive function. ⁵ Smith (2017) ⁶ reported that cognitive impairment is usually seen in any vestibular dysfunction such as either peripheral or central vestibular dysfunction.

The P300 is an event-related potential, elicited when the target stimuli in the odd-ball paradigm is identified by the participant. It serves as an index for the assessment of cognitive ability to assess cerebral information processing in the context of various neurological diseases. ⁷ Several studies have documented abnormal P300 in individuals with cognitive dysfunctions such as autism spectrum disorder, ⁸ attention deficit hyperactivity disorder, ⁹ schizophrenia, ¹⁰ and migraine. ¹¹ It is usually performed with minimum attention to the stimuli and without secondary tasks. The P300 is used to evaluate age-related cognitive dysfunction, reflecting attention and memory processes and overlapping function in cognitive deficit. ¹² Different areas of the brain that provide the generation of P300 response include subcortical structures, auditory regions in the cortex and frontal lobe and various association areas neocortex. ¹³ The subcomponents for P300, P3a is generated from the frontal working memory which helps in early attention whereas P3b is an attention-driven stimulus generated from the temporal and parietal structures. ⁷ The P300 amplitude response mainly depends on stimulus probability, stimulus significance, task effort, motivation, and attentiveness. ¹⁴ P300 amplitude is directly related to the amount of attention paid to perform a particular task associated with superior memory performance. ¹⁵ P300 latency reflects stimulus processing time in contrast to response processing time, which corresponds to stimulus evaluation time and is independent of the response section. ^{16 , 17}

In the case of individuals with vertigo, the literature has reported reduced behavioural cognitive abilities. ¹⁸ A national health and nutrition examination survey done in the US revealed an association between vestibular and cognitive function in the adult population. ⁵ There is a steady accumulation of evidence that the vestibular lesion leads to a cognitive deficit. It is not essentially directly related to reflexive signs and perceptual disturbances associated with vestibular dysfunction. ¹⁹ And there is minimal scientific evidence on cortical potentials in individuals with vestibular dysfunction. Hence, the current study aims to compare the findings of cortical potentials (P1, N1, P2, and N2) and cognitive potentials (P300 and N4) between individuals with and without vestibular dysfunction. The objective was to investigate the relationship of cortical and cognitive potentials peak latency and peak amplitude in individuals with and without vestibular dysfunction and the correlation between DHI score with P300 findings among individuals with vestibular dysfunction.

The grand averaged waveforms for standard and deviant stimuli for both groups are shown in Figure 1. In the figure, it is evident that both pure-tones elicited obligatory P1-N1-P2 response for the stimulus onset among participants in both groups. Further, the waveform for target stimuli showed a large positive peak at a latency of 280 ms following the P1-N1-P2 response in both groups of participants, referred to as P300. The identification rate of peak responses varied across groups at Cz and Pz positions, which is depicted in Figures 2 and 3 respectively. The P300 was absent in a greater number of individuals with vestibular dysfunction compared to the control group. To investigate the association between vestibular dysfunction and P300, a chi-square test was carried out. The result showed a statistically significant association between vestibular dysfunction and the presence or absence of P300 (χ ²(1) = 8.53, p = 0.003) with an odd ratio of 15.83.

Table 1 shows the mean latency of peaks P1, N1, P2, and N2 at electrode sites Cz and Pz for both groups. The mean latency of peaks P1, N1, P2, and N2 were similar between groups at the electrode sites Cz and Pz. To investigate if the mean latency of peaks were significantly different between groups, the independent t-test was carried out. It showed no significant difference for the latency of peaks P1 [t(37) = -1.083, p = 0.286)], N1 [t(37) = -1.008, p = 0.320)], P2 [t(36) = 1.007, p = 0.321)], and N2 [t(32) = 1.822, p = 0.078)] at the electrode site Cz. Similarly, at Pz the latency of peaks P1 [t(28) = -0.029, p = 0.977)], N1 [t(31) = -0.029, p = 0.977)], P2 [t(30) = -1.059, p = 0.298)], and N2 [t(27) = 0.56, p = 0.956)] were not significantly different between groups.

Table 2 shows the mean amplitude of peaks P1, N1, P2, and N2 at electrode sites Cz and Pz for both groups. The mean amplitude of peaks was larger in individuals with no vestibular dysfunction (group II) at both Cz and Pz. To investigate if the mean amplitudes of peaks are significantly different between groups, independent t-test was carried out separately for Cz and Pz. It revealed no significant difference for the amplitude of peaks P1 [t(30) = -2.733, p = 0.10)], N1 [t(37) = -0.614, p = 0.543)], P2 [t(36) = -1.061, p = 0.296)] and N2 [t(32) = -0.268, p = 0.790)] at the electrode site Cz between groups. Similarly, the amplitude of peaks P1 [t(28) = -1.742, p = 0.093)], N1 [t(31) = -1.326, p = 0.194)], P2 [t(28) = -1.742, p = 0.093)] and N2 [t(27) = -0.318, p = 0.756)] at the electrode site Pz showed no significant difference between the groups. On peak-to-peak analysis between groups showed no significant difference in P1-N1 and N1-P2 peak to peak amplitude at Cz and Pz.

Table 3 shows the mean latency and amplitude of peaks P300 and N4 at Cz and Pz for both groups. A noticeable difference was observed for the mean amplitude of N4 between groups at both the electrode sites. The mean amplitude of P300 was larger in group I compared to group II, this finding is controversial when compared to the grand average waveform of both groups shown in Figure 1. The mean amplitude of P300 was found to be largest in group 1 compared to group II. To investigate if the mean difference for latency and amplitude were significantly different between groups, an independent samples t-test was carried out. The results showed no significant difference in the latency of P300 [Cz: t(32) = -0.173, p = 0.866); Pz: t(30) = -0.357, p = 0.724)] and amplitude of P300 [Cz: t(32) = 0.218, p = 0.829); Pz: t(29) = 0.797, p = 0.432)] at both Cz and Pz. Whereas no statistical significant difference was found for the N4 latency [Cz: t(16) = 0.415, p = 0.684); Pz: t(16) = 0.786, p = 0.443)] and significant difference was observed in N4 amplitude [Cz: t(14) = -2.178, p = 0.047); Pz: t(15) = -2.107, p = 0.052)] at both positions.

To investigate the relationship between the latency of P300 and DHI score, Pearson’s correlation analysis was carried out. The results showed a weak negative correlation between the latency of P300 and the DHI score; however, the correlation was not significant at both electrode sites [Cz: r = -0.201, p = 0.490; Pz: r = -0.401, p = 0.196]. Further, no correlation was found between the amplitude of the P300 and DHI score at both electrode sites [Cz: r = -0.167, p = 0.569; Pz: r = 0.087, p = 0.787].

The mean latency of late latency response and P300 of individuals diagnosed with peripheral vestibular lesion and central vestibular lesion are depicted in Tables 4 and 5 respectively.

The present study compared the latency and amplitude of cortical (P1, N1, P2 and N2) and cognitive potentials (P300) among individuals with and without vestibular dysfunction. The cortical potential includes auditory late latency responses P1, N1, P2, and N2. As per a review, it is clear that cognitive impairment is observed in individuals with vestibular dysfunction, with respect to attention, spatial orientation, executive function and memory. ⁵

The results of the present study showed no significant difference in the latency and amplitude of peaks P1, N1, P2, and N2 of the cortical auditory potentials. These findings are not in agreement with results of earlier investigation. ²² However, findings of the present study could be explained based on the hearing sensitivity of participants in both groups and the characteristics of the P1-N1-P2 response. The P1-N1-P2 response is elicited for the onset of stimuli, therefore, the characteristics of the response are dependent on the onset of the stimuli. Further, the participants in both groups had hearing sensitivity within normal limits. Thus, the latency and amplitude of the peaks are expected to be similar in both groups.

The P300 was found to be absent in a greater number of individuals with vestibular dysfunction compared to the control group. It was absent in 30–40% of the individuals with vestibular dysfunction; this finding is consistent with the results of the previous study. ²³ Further, when the P300 was present, the mean latency and amplitude of the P300 in both groups were similar. In contrast to the findings of the present study, earlier investigations have reported prolonged latency for P300 in individuals with vestibular dysfunction compared to the control group. ^{20 , 22} The contrasting findings observed in the present study and earlier investigations could be because of differences in the site of vestibular lesion across studies. Studies in the literature have included individuals with peripheral vestibular lesions where the site of the lesion was localized to the lateral semicircular canal. ^{24 , 25} The majority of the participants were reported to have unilateral caloric hypofunction. The findings of the above investigations showed prolongation of P300 latency in individuals with unilateral peripheral vestibular lesions (lateral semicircular canal) compared to the control group. In contrast, participants in the present study had peripheral vestibular lesion with abnormal findings on cVEMP and oVEMP indicating a lesion in the saccule and utricle. Therefore, the contrasting findings observed in the present study could be a consequence of differences in the site of the lesion. In addition, contrasting findings observed in the present study could be due to the degree of dizziness handicap. The majority of the participants with peripheral vestibular lesion in the present study were found to have mild handicap based on DHI scores. The degree of handicap might have an influence on the latency and amplitude of P300.

Studies on cognitive function assessment using a cognitive failure questionnaire in individuals with vestibular dysfunction revealed that cognitive dysfunction is prevalent in individuals with central and peripheral vestibular pathologies. ²⁶ The literature also showed a positive correlation between cognitive dysfunction and dizziness handicap in terms of a self-rated questionnaire. DHI helps in evaluating the dizziness handicap based on its impact physically, functionally, and emotionally with a limited profile on cognition. ²⁷ In the current study, the correlation between DHI scores and P300 showed no significant correlation. The lack of correlation between the two measures could be due to the different areas of assessment. DHI is a measure of self-help obtained primarily based on daily activities, whereas the P300 is an electrophysiological measure that assesses cognitive functioning. ¹³ Because of this direct correlation between DHI and P300 was found to be inconclusive in the present study. Similarly, no significant correlation was observed between P300 and vertigo symptoms, whereas another study stated that severity of vestibular symptoms seems to correlate with P300 responses. ²⁸ In support of the current study, a randomized controlled trial showed cognitive behaviour therapy influenced patients with chronic subjective dizziness with a significant reduction in DHI and no changes in psychological outcome measures. ²⁹ Similarly, other literature has reported that the functional and physical parameters of DHI showed a negative correlation, and the emotional parameter showed a weak significant positive correlation in 369 participants evaluated for functional tests such as electronystagmography, rotational testing, and platform posturography. ³⁰ The findings of various studies by several investigators have emphasized the role of the vestibular system’s role on cognition, such as perceptual/visuospatial ability, memory, attention, and executive function. Knowing the cognitive function of individuals with vestibular dysfunction facilitates the setting of vestibular rehabilitation therapy goals. Evidence reveals that in patients with intractable dizziness following vestibular rehabilitation there is a significant improvement in vestibular function and cognitive function including attention, visuospatial ability and executive function with coincidental improvement in DHI. ³¹ The findings of this study are circumscribed to oddball auditory tasks only, which might be a limitation. The majority of participants in the present study had mild handicap, this might have an influence on the findings.

In the present study, the P300 was absent in a greater number of individuals with vestibular dysfunction, suggesting cognitive impairment. However, when the P300 was present, the peak latency and amplitude were not significantly different in both groups.

Written informed consent for publication of the participants’ details was obtained from the participants.