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            | OJHAS Vol. 10, Issue 2: 
            (Apr-Jun 2011) |  
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            | Effect of Intensity 
on Prevalence of N3 Potential in Ears with Severe to Profound Hearing 
Loss |  
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                | Kaushlendra Kumar, Jayashree S. Bhat,
 Ashwini S. Guttedar,
 Department of Audiology & Speech 
Language Pathology, Kasturba Medical College (Manipal University), Mangalore, India
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                | Kaushlendra Kumar,
          
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            |  |  | Address for Correspondence | Assistant Professor,
 Department of Audiology & Speech 
Language Pathology,
 Kasturba Medical College (Manipal University),
 Attavar, Mangalore - 575001,
 India.
                
                
            E-mail:  
            
                kaushlendra84@rediffmail.com
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            Kumar K, Bhat JS, Guttedar AS.
             Effect of Intensity 
on Prevalence of N3 Potential in Ears with Severe to Profound Hearing 
Loss. Online J Health Allied Scs. 
            2011;10(2):17 |  
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            | Submitted: Apr 27, 
            2011; Accepted: Jul 15, 2011; Published: Jul 30, 2011 |  
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            | Abstract: |  
            | Objective of the 
study: To look for the presence of N3 potential at two different 
intensities in children and in   adults.
Method: A total of 
260 ears with severe to profound hearing loss 
were studied from the participants 
in the age range of 1 to 50 years, with 170 subjects in the age group 
 below 10 years and remaining 90 subjects 
 of more than 10 years. Auditory brainstem response (ABR) was recorded at two 
intensities, 90 and 99dBnHL, to look for the presence of N3 potential.
Result:  N3 potential was observed in 30% of the 
total ears taken in the study at 90dBnHL and 38.8% at 99dBnHL. Presence 
of N3 potential in children was 45%, 
which was higher than the age group of above 
10 years. When the intensity was increased there was an increase in 
amplitude and a reduction in latency with better wave morphology.
Conclusion: It is 
better to use higher intensity for the identification 
of  the N3 potential while doing ABR and thus with the 
 single recording, auditory assessment as well as saccular assessment can be done.Key Words: 
  N3 
potential; Auditory brainstem response; Saccular origin
 |  
            |  |  The 
auditory brainstem response (ABR) allows one to objectively gauge peripheral 
hearing acuity as well as neurological abnormalities in the auditory 
brainstem pathway. It serves an important role in the testing of physiological 
function. Neural responses to acoustic stimuli could 
be recorded after destruction of cochlear hair cells in guinea pigs, the 
          response probably originating from the saccule of 
the vestibular system. The results of these animal experiments suggested 
that a vestibular evoked response to acoustic stimulation can be recorded 
in humans.(1-3)  A 
large negative deflection with a latency of 3ms in the ABR wave forms 
of some patients with profound deafness of peripheral origin. This negative deflection 
          has been termed as the N3 potential, and it has been assumed that the N3 
potential might be a vestibular-evoked potential to acoustic stimulation, saccule 
          being the most likely site 
of origin.(4) It has been 
reported that as the stimulus intensity increased, the amplitude of the 
potential increased and the latency decreased.(4) It has also been stated that 
N3 potential could be recorded from all electrode placements, and the amplitudes 
and latencies were almost consistent, and no polarity inversion was observed 
over the scalp.(4) N3 potential is reported to be widely distributed over the 
scalp, rather than being limited to the stimulated side. This means that an N3 
potential has a far-field nature similar to an ABR. Manabe et al (5) also 
recorded a potential similar to the N3 potential, and indicated that this 
potential is not an artifact which might be due to any particular recording 
condition or equipment,  but that it arises as a physiological neural 
response to a loud stimulus sound and this is well supported by the important 
fact that the latency decreases when the stimulus becomes louder and prolonged 
when a higher repetition rate is used.(5) Acoustically 
evoked short latency negative response (ASNR) was found only in profound 
hearing loss ears under intense stimuli (80 to 120dBnHL). Click-evoked ASNRs 
were present in 12.3% patients (11.9% ears), having neural response characteristics, that 
is the latency and amplitude shortened and increased respectively in 
response to the change in the stimulus intensity.(6) N3 potentials 
were recorded by Ochi K et al in 41.7% ears and VEMP was detected in 66.7% ears in subjects 
having hearing threshold ranging from 65 to above 110dB.(7) They suggested 
that although VEMP and N3 potential appear to originate from   saccule,  the characteristics of these two responses 
being not identical, the mechanisms 
responsible for the generation of these two responses are somewhat different, 
so that an additional factor might exist for the generation of the N3 
potential.(7) It 
is clear from the literature that N3 potential has not been studied 
extensively. Moreover the effect of different intensities on the occurrence 
of N3 potential has not been focused in any of these studies. The present 
study was taken up with an aim to look for the presence of N3 potential 
and the latency and amplitude effect at two different intensities, 90 
and 99dBnHL,  in ears having severe to profound hearing loss. The second 
aim of the present study is to see the presence of N3 potential in two 
age groups, children and adults at 99dBnHL. This is a retrospective study involving 260 subjects 
        with severe to profound hearing loss ears (160 subjects), with age 
        ranging from 1 year to 50 years. Auditory brainstem response (ABR) data 
        were collected during June 2005 to May 2009 and was analyzed for N3 in 
        all the subjects. A total of 170 ears were having 
age range below 10 (mean age 4.2 years) and remaining 90 ears were more than 10 years old (Mean age 21.3 years). 
        The following subject selection criteria were adopted for the study:  
  Hearing loss of severe to 
  profound degree and of sensory neural type.The absence of ABR responses 
  at 99dBnHL.Absent distortion product 
  otoacoustic emission (DPOAE).None of the subjects had recent 
  history or presence of any otological problem (like ear discharge, ear 
  ache etc) or any neurological symptoms.‘A’ type tympanogram with 
  absent ipsi and contra reflexes. Procedure All the procedures 
were executed in a soundproof room. Initially each subject  underwent 
a pure tone audiometry across octave frequencies from 250 to 8000 Hz 
for air conduction and from 250 to 4000 Hz for bone conduction using 
GSI-61 audiometry and same instrument was used for Behavioral Observation 
Audiometer (BOA). BOA was performed using ascending method for 0.5, 
1, 2, and 4 KHz frequencies. Subjects below 2 years  underwent BOA 
and above 2 years either went for conditioning audiometry 
or pure tone audiometry. Subsequently tympanogram and acoustic reflexes 
were established using 226 Hz probe tone using GSI Tympstar. Acoustic 
reflex threshold were obtained for ipsilateral and contralateral for 
0.5, 1, 2, and 4 KHz frequencies. GSI-Audera DPOAE was performed for 
all the subjects for 1, 1.5, 2, 3, and 4KHz. GSI-Audera instrument was 
used for recording of auditory brainstem response. 
| Table 1: Acquisition 
and stimulus parameters used to record the ABR. |  | Analysis time | 15 msec |  | Filter setting | High pass: 30Hz or 100Hz Low pass: 1500Hz or 3000Hz
 |  | Gain | 100000 |  | Type of stimulus | 100 µsec click as well as 0.5 KHz tone 
  burst with 2-cycle rise/fall time. |  | Rate | 30.1 |  | Polarity | Rarefaction |  | Intensity | 90 and 99dBnHL |  | Total number of stimulus | 1500 |  | Electrode montage | Non-inverting electrode (+): vertex(Cz) Inverting electrode (-): 
  Test ear mastoid(M1 /M2)
 Ground electrode: forehead(Fz)
 |  ABR 
was done at two intensity levels, 90 and 99dBnHL. The N3 potential was 
visually detected by two experienced clinical audiologists at both the 
levels. Obtained data was analyzed in terms of percentage of occurrence 
of N3 potential and to see the differences between two intensity levels 
the chi-squared test was administered. In 
the present study, a total of 260 ears were studied at two different 
intensities, 90 and 99dBnHL. Almost 65% of the subjects were children, 
younger than 10 years. 
  | Table 2: Presence of N3 
potential at different intensities |  | Intensity (dBnHL) | Total number of ears | Total number of ears with presence of 
  N3 potential | Presence of N3 potential in 
  percentages | Absence of N3 potential in 
  percentages |  | 90 | 260 | 78 | 30% | 70% |  | 99 | 260 | 101 | 38.8% | 61.2% |  As 
it can be seen, N3 potential was observed in 30% of ears at 90dBnHL 
and 39% at 99dBnHL. So the trend observed was, as the intensity increased 
from 90 to 99dBnHL, there was an increase in the presence of N3 potential. 
It was also observed that all the subjects who had N3 potential at 90dBnHL 
also showed the presence of N3 potential at 99dBnHL. 
| Table 3: Prevalence of 
N3 potential at 99dBnHL in two different age groups. |  | Age group | Total number of ears | Presence of N3 potential in percentages | Absence of N3 potential in percentages |  | Below 10 years | 170 | 76(44.7%) | 94(55.2%) |  | Above10 years | 90 | 25(27.7%) | 65(72.2%) |  Table 3 shows that in children the presence of N3 potential 
  is 45% which is higher than the age group of above 10 years, among whom only 
  28% had N3, suggesting that children have higher incidence of N3 potential 
  than adults at the same intensity. 
| Table 4: Mean and standard 
deviation of latency and amplitude at two different intensity 90 and 
99dBnHL. |  | Intensity | VEMP parameters | Mean | Standard deviation |  | 90 | Latency | 3.12msec | 0.17 |  
  | Amplitude | 172.89nV | 64.37 |  | 99 | Latency | 3.04mesc | 0.15 |  
  | Amplitude | 265.08nV | 75.75 |  As 
depicted in Table 4, as the intensity increased from 90 to 99dBnHL, 
the latency was reduced from 3.12 to 3.04 msec and there was an increase 
in amplitude from 172 to 265 nanovolt. The standard deviation of the 
N3 potential latency was less, but the standard deviation of amplitude 
was high. The Chi-squared test was administered to see the significance of 
difference between two different intensities at 90 and 99dBnHL. The 
chi-squared test  for latency is 671.58 with an associated 
p<0.005, suggesting a significant difference in latency 
between 90 and 99dBnHL. The chi-squared test  for amplitude 
is 1263.87 with an associated p<0.005, suggesting a statistically significant difference between the two intensity levels. Raw scores indicated a slight difference in amplitude between the two 
intensities. In 
the present study, N3 potential was present in 30% of the ears taken 
at 90dBnHL and in 39% ears at 99dBnHL. Ochi K et al (7) reported the  detection of 
N3 potential in 41.7% of the total ears whereas  in the present 
study N3 potential was observed in 39% of ears. This may be due to the difference in stimulus intensity used, which was 
105dBnHL in Ochi et al compared to 99dBnHL in the present study. This indicates that the 
stimulus intensity plays a role in the occurrence of N3 potential. The 
absence of N3 potential in many subjects could be attributed to the 
individual variation of vestibular function, particularly under unphysiologic 
stimulation. Nong DX (6) reported that the N3 potential were present 
in 11.9%. The   lesser percentage of the presence of N3 potential in 
their study is due to the intensity used which was between 80 and 120dBnHL.(6) It 
was also observed  in the present study that as the intensity increased, 
there was an increase in amplitude and reduction in latency. Kato T et al (4) 
had reported two case reports in which as the intensity was increased, there was 
an increase in amplitude and a decrease in the latency. Nong DX (6) also 
reported that the N3 potential had neural response characteristics as the 
latency and amplitude being shortened and increased respectively in response to 
the change in the stimulus intensity. In 
the present study, 45 % of the children below 10 years had the presence of N3 
potential and 28% of the participants above 10 years of age showed the presence 
of N3 potential. In contrast Nong DX (6) reported significantly higher 
appearance rates in young subjects especially in the 20 to 30 years group. In 
the present study, the higher rate of occurrence of N3 potential in children 
might be due to the higher sound pressure level generated at tympanic membrane 
as the ear canal volume is less for children than adults. The sound pressure 
level changes might cause the presence of more N3 potential in children than in 
adults. In 
conclusion it can be put forth that as the intensity increases, there 
is higher rate of the presence of N3 potential with a shorter latency 
and higher amplitude. The presence of N3 potential is higher in children 
than in adults. It is better to use a higher 
intensity in  identifying N3 potential while doing ABR so 
that auditory assessment as well as saccular assessment can be done at the same 
recording in subjects with severe to profound hearing loss. 
    Cazals Y, Aran J, Erre J, Guilhaume A. ‘Neural’ responses to acoustic stimulation after destruction 
  of cochlear hair cells. Eur Arch OtoRhinolaryngol. 1979;224:61-70.Cazals Y, Aran J, Erre J, 
  Guilhaume A. Acoustic responses after total destruction 
  of the cochlear receptor: Brainstem and auditory cortex. Sci. 1980;210:83-86.Cazals Y, Aran J, Erre J, 
  Guilhaume A, Aurousseau C. Vestibular acoustic reception in the guinea 
  pig: A saccular function? Acta Otolaryngol (stockh). 1983;95:211-217.Kato T, Shiraishi K, Eura 
  Y, Shibata K, Sakata T, Morizono T, Soda T. A ‘Neural’ response 
  with 3-ms latency evoked by loud sound in profoundly deaf patients. 
  Audiol Neurootl.1998; 3:253-264.Manabe T, Nishizawa N, Koba 
  K. A reliability of auditory brainstem response test in profoundly deaf 
  children. Audiol Jpn. 1982;25:433-434Nong DX, Ura M, Owa 
  T, Noda Y. An acoustically evoked short latency negative response in 
  profound hearing loss patients. Acta Otolaryngol. 2000;120:960-966.Ochi K, Ohashi T, Nishino 
  H. Variance of vestibular-evoked myogenic potentials. Laryngoscope. 
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