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OJHAS Vol. 7, Issue 1: (2008
Jan-Mar) |
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DPOAE in
HIV infected adults |
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Rajesh Ranjan, Lecturer in Audiology & speech Language pathology,
Department of audiology and speech language pathology,
Kasturba Medical College, (A unit of Manipal University),
Mangalore-575001 Jayashree S. Bhat, Professor and Head,
Department of Audiology and Speech Language pathology, Kasturba Medical College, (A unit of Manipal University),
Mangalore-575001 |
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Address For Correspondence |
Rajesh Ranjan, Lecturer in Audiology & speech Language pathology,
Department of audiology and speech language pathology,
Kasturba Medical College, (A unit of Manipal University),
Mangalore-575001
E-mail:
raj_rajmillinum@yahoo.co.in |
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Ranjan R, Bhat JS. DPOAE in
HIV infected adults. Online J Health Allied Scs. 2008;7(1):9 |
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Submitted Oct 29, 2007; Accepted:
Mar 14, 2008; Published: Apr 10, 2008 |
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Abstract: |
HIV infection
is associated with impairment of hearing function, at any stage of disease
causing complication to the external, middle, inner ear
and CNS. Audiological manifestation of HIV is a direct consequence
of virus or secondary to the pharmacological treatment or viral complication.
Objectives:
There is paucity of information pertaining to hearing status in HIV.
As the deafness can occur at any stage of HIV with varying degree and
people with HIV live longer, there is need to address the hearing problems
in these individuals. So this study aimed detecting the outer hair cell
functioning by doing DPOAE in normal hearing HIV infected adults.
Method: The experimental group comprised of
12 HIV infected (24 ears) within 20 to 40 years. The
age matched control group comprised of 15 subjects (30 ears).
All the subjects had normal hearing sensitivity. Initially puretone
audiometry and immittance was performed for the subject selection. Subsequently
DPOAE procedure was done.
Results:
The DPOAE was abnormal in 50% of the subjects.
Conclusion:
It can be concluded that the cochlear involvement is a common observation
in HIV infected individuals. DPOAE test
can be used as a tool for early identification of cochlear pathology
in HIV infected.
Key Words:
HIV, DPOAE, Outer hair
cell function, Central nervous system |
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Although education
about Acquired immune deficiency syndrome (AIDS) is spreading faster
than the disease itself, and the ways to avoid infection are well known,
AIDS continues to be one of the world’s greatest health problems.
A substantial number of HIV infected patients experience long term disabilities
involving cognitive and motor functions, which include communication
disorders.(1-4) HIV infected individuals who eventually develop AIDS
may remain asymptomatic for an average of 8 – 10 years.(5) Otologic
manifestations associated with HIV infection are mild hearing impairment
present at any stage of disease with complication anywhere in the auditory system from external ear
to the CNS.(6-8) Most otologic problems are caused by routine organisms
and respond to standard therapy.(9) Audiological problems of HIV infection
is considered as a direct consequence of virus or secondary to the pharmacological
treatment.(10) Due to the involvement of central nervous system in HIV
infection, the most direct consequence to the auditory system is central
auditory nervous system abnormalities, measured with auditory brainstem
response (ABR). ABR finding in adults with HIV include prolonged absolute
latency of third and fifth or IPLs of I-III, I–V.(11,12) There is
growing evidence of both central and peripheral hearing loss associated
with opportunistic infections such as primary CNS lymphomas.(1,9,13)
Sooy
reported that 45% of out of 53 patients had sensorineural hearing loss
in AIDS.(14) Sensorineural hearing loss reported in persons with HIV
infection ranged from 20.9 to 49%.(9) The exact cause and site of lesion
for sensorineural hearing loss associated with HIV disease is unknown.
Sensorineural hearing loss associated with HIV may be caused by secondary
opportunistic infections of the CNS or many of the drugs used to treat
HIV infection with its ototoxic complications. Another form of therapy
that may cause sensorineural hearing loss is the use of radiation to
treat CNS lymphomas associated with HIV.(9)
Otoacoustic
emission is a non invasive procedure which enables one to identify the
cochlear component of a hearing disorder and to objectively monitor
minute changes in cochlear status undetectable by other audiological
procedures. Its clinical utility ranges from detection of noise induced
hearing loss, to check the extent of damage of outer hair cells in ototoxicity,
to differentiate between cochlear and retrocochlear pathology, to diagnose
functional hearing loss, auditory neuropathy etc. Oto acoustic emissions
arise from the most vulnerable cellular mechanism in the ear, which
is of fundamental importance to hearing, the outer hair cells.(15-17)
and therefore are particularly useful in assessing damage caused by
HIV infection. It has been shown that otoacoustic emissions can be recorded
in almost all the normal hearing individuals.(18,19) As the hearing
thresholds increase, the possibility of recording normal OAEs gets significantly
reduced. The hearing thresholds beyond which the emissions may be absent
is variable across studies, from 15 dB HL (20), 25 dB HL (21),
35 dB HL (22) to 40 dB HL.(23,24)
HIV
infected individual has often prescribed medications as a prophylaxis
or treatment of opportunistic infections that have been long associated
with the development of audiological (tinnitus, vertigo, dizziness,
auditory disturbances, deafness, decreased hearing, hearing loss, and
otalgia) and vestibular changes regardless of a persons HIV status.
The severity of ototoxic induced hearing impairment varies from patient
to patient and depends upon the sensitivity of the individual, the size
of the dosage, and/or the length of time the drug has been taken.
Beyond ototoxicity many of the opportunistic infections are associated
with the development of hearing loss. Sudden onset sensorineural hearing
loss also has been reported in the HIV/AIDS populations and deserves
special considerations, as this particular population is susceptible
to numerous opportunistic infections, approximately one third of patients
with sudden sensorineural hearing loss have some history of recent viral
infection.(25)
Need of
the study
However
a review of the literature in Audiology revealed a paucity of information
pertaining to hearing status in HIV. As the deafness can occur at any stage of
HIV with varying degree and people with HIV live longer, there is a grave need
to address the hearing problems in these individuals in order to help them
maintain a productive and meaningful life for as long as possible. The early
detection of possible underlying hearing pathology helps in drawing a meaningful
intervention plan and so this study was taken up with an aim of detecting the
outer hair cell functioning by Distortion product otoacoustic emissions (DPOAE)
in normal hearing HIV infected adults.
The
study was conducted at a tertiary care hospital.
Subjects:
Control
group comprised of a total number of 15 subjects (30 ears) between 20
to 40 years. All the subjects in the control group had normal hearing
sensitivity, and none of them had otologic abnormalities. Twelve subjects
(24 ears) with HIV infection comprised the experimental group within
the age ranging from 20 years to 40 years. All the subjects had normal
hearing sensitivity with ‘A’ type tympanogram and normal reflexes
bilaterally.
Instrumentation:
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GSI 61 Audiometer was used to evaluate the hearing sensitivity.
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GSI Tymp star was used to analyze the middle ear function.
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GSI Audera was used to record the DPOAE.
Procedure:
All the procedures
were carried out in a sound treated room. Initially a detailed history
was obtained. All the subjects had otoscopic examination. This was
followed by pure tone audiometry and immittance testing for the subject
selection. Subsequently, the DPOAE screening was performed with the
following parameters
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L1/L2 -
65/55
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F1/F2 -
1.22
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DP frequency
-1KHz, 1.5KHz, 2KHz, 3KHz, 4KHz
Analysis
Obtained
data was analysed in percentages by comparing the signal to noise ratio
between the control group and the experimental group for different frequencies.
This
study was aimed at screening HIV with DPOAE to assess the outer hair
cell function in normal hearing HIV infected adults. Almost 50% of the
subjects demonstrated OAE abnormality in this study. Out of the 12 ears
taken for study, otoacoustic emission amplitude were reduced in 50%
at 1KHz, 41.66% at 1.5kHz , 25%at 2kHz, 33.33%at 3kHz and 41.66% at
4kHz. It was also observed that in 16.66% OAE was almost absent in all
frequencies in spite of having normal hearing sensitivity. The results
are detailed in Table I.
Table I: Signal to noise ratio (S/N) of Distortion Product Otoacoustic Emission
at different frequencies in HIV infected individuals
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1kHz |
1.5kHz |
2kHz |
3kHz |
4kHz |
S1 |
7.57 |
11.24* |
21.41 |
19.78 |
17.83 |
S2 |
6.34* |
9.53* |
17.03 |
15.01 |
11.85* |
S3 |
10.20 |
22.23 |
20.14 |
21.70 |
24.36 |
S4 |
3.21* |
27.37 |
7.59* |
27.91 |
33.50 |
S5 |
17.59 |
24.60 |
23.41 |
11.61* |
.00** |
S6 |
.00** |
16.10 |
22.42 |
10.83* |
1.84* |
S7 |
18.02 |
22.73 |
22.63 |
18.95 |
17.67 |
S8 |
23.38 |
12.68 |
22.87 |
20.57 |
32.35 |
S9 |
1.50* |
11.24 |
21.41 |
19.78 |
17.83 |
S10 |
18.02 |
22.73 |
22.67 |
18.95 |
17.67 |
S11 |
6.09* |
.00** |
.00** |
.00** |
.00** |
S12 |
6.31* |
.88* |
.00** |
1.87* |
.00** |
S13 |
7.37 |
11.14* |
21.35 |
19.77 |
17.82 |
S14 |
6.29* |
9.44* |
17.30 |
15.54 |
11.55* |
S15 |
10.29 |
22.44 |
20.36 |
21.85 |
24.56 |
S16 |
3.18* |
27.55 |
7.48* |
27.63 |
33.06 |
S17 |
17.78 |
24.44 |
23.23 |
11.57* |
.00** |
S18 |
.00** |
16.33 |
22.46 |
10.77* |
1.82* |
S19 |
18.34 |
22.53 |
22.43 |
18.65 |
17.66 |
S20 |
23.28 |
12.54 |
22.67 |
20.56 |
32.25 |
S21 |
1.44* |
11.44 |
21.21 |
19.88 |
17.34 |
S22 |
18.22 |
22.87 |
22.76 |
18.96 |
17.76 |
S23 |
6.11* |
.00** |
.00** |
.00** |
.00** |
S24 |
6.41* |
1.11 * |
.00** |
1.89* |
.00** |
Normative
with SD |
13.24 (SD-6.22) |
19.03 (SD-7.16) |
19.89 (SD-9.22) |
21.70 (SD-7.65) |
24.66 (SD-8.10) |
% of abnormal
OAE findings |
50% |
41.66% |
25% |
33.33% |
41.66% |
* reduced amplitude; ** absent amplitude
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The present
study focused on assessing the outer hair cell function by doing DPOAE
in HIV infected adults. A clear indication of cochlear involvement was
observed in 50% of the subjects included in the study. This is in consensus
with Sooy, who reported that 45% out of 53 patients diagnosed with AIDS
had sensorineural hearing loss.14 Lalwani and Sooy have reported
sensorineural hearing loss in persons with HIV-1 infection ranging from 20.9 to
49%.(9)
Probst et al
have reported that otoacoustic emissions can be recorded in almost all
the normal hearing individuals.(18,19). As the hearing thresholds increase,
the possibility of recording normal OAEs gets significantly reduced.
The hearing thresholds beyond which the emissions may be absent is variable
across studies, from 15 dB HL (20), 25 dB HL Probst et al (21),
35 dB HL (22), to 40 dB HL.(23-24) The fact that all these subjects had normal hearing with abnormal OAE
could be attributed to cochlear pathology either due to ototoxicity
or HIV infection itself.
The amplitude
difference with low and high frequency regions being more affected than that of
mid frequency was observed in this study. Shaffer et al.(26) have commented that
in normal hearing subjects the relative amplitudes of the generation and
reflection components vary across frequency, with some frequency regions having
greater amplitude of the generation component while in other frequency regions
the reflection component may dominate.
Consequence of HIV
infection on the auditory system is central auditory
nervous system abnormalities, some of which can be measured with auditory
evoked potential which include mainly ascending pathway i.e. afferent
pathway. ABR finding in adults with HIV include prolonged absolute
latency of third and fifth or IPLs of I-III, I–V(11-12), which
indicate problem in the auditory path way. As 95 % of the ascending
nerve fibers supply to the IHCs and 5% to the OHCs, and in the efferent
nerve fibers, 90 % to the OHCs and 5% to the IHCs, there is a possibility
that efferent pathway may also be effected, which may lead to impaired
OHC function, as it controls the outer hair cells function. The same
may be applicable in the present study too.
However
there are hardly any studies done on the HIV infected with a special
focus on the ototoxic effect of the disease on the auditory system.
Otologic manifestations associated with HIV-1 infection are mild hearing
impairment present at any stage of disease with complication anywhere in the auditory system from external ear
to the CNS.(6-8) The fact that the integrity of the outer hair cells
is questionable in HIV infected even when the hearing function is normal
stresses on the importance of DPOAE screening which helps in the early
detection so that possible intervention strategies can be initiated. As primary professionals in hearing health care,
audiologists have responsibilities to inform themselves and other relevant health-care professionals about
any of the issues associated with HIV/AIDS.(27)
The
present study was an attempt towards assessing the integrity of the
auditory system particularly the outer hair cell function in HIV infected
adults. It was observed that the OAEs were abnormal in 50% of the subjects
in spite of having normal hearing ability, indicating cochlear involvement.
The attributing factor for this abnormality could be the HIV infection
itself or the ototoxic effect of the medication. With a lot of stress
on the longer life span of the HIV infected, it is mandatory to identify
problems at the earliest for drawing a meaningful intervention plan.
Hearing is one of the important functions that play a major role in
all walks of life. DPOAE thus can be used as a tool for the early identification
of cochlear pathology in individuals with HIV infection, even prior
to the hearing sensitivity being compromised because of the infection.
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