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Therapies for Hearing Loss

A special issue of Journal of Clinical Medicine (ISSN 2077-0383). This special issue belongs to the section "Otolaryngology".

Deadline for manuscript submissions: closed (1 April 2020) | Viewed by 167846

Special Issue Editor


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Guest Editor
1. Departments of ENT (Hôpital Edouard herriot and Hôpital Femme Mère Enfant), Centre Hospitalier et Universitaire de Lyon, Lyon, France
2. Department of Audiology and Otorhinolaryngology, Edouard Herriot Hospital, Lyon 1 University, 69437 Lyon, France
3. INSERM U1028 - CNRS UMR5292, Lyon Neuroscience Research Center, Equipe IMPACT, Lyon, France
Interests: cochlear implants; middle ear surgery; deafness; auditiory implants
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

It is my pleasure to invite you to submit papers for a Special Issue of the Journal of Clinical Medicine focused on “Therapies for Hearing Loss”.

Deafness is a major handicap, impending social, emotional, and professional life of millions of people, in an entire lifespan. Babies can be screened at birth and treated very efficiently to date; these major advances in care of deafness in children improve dramatically their well-being. It has been demonstrated that hearing loss can impact cognitive skills in the elderly and that auditory rehabilitation can reduce this impact.

Improvements in knowledge have been very important in the last few decades in the fields of genetics, bioengineering, and auditory function assessment. These have led to possible new therapies for hearing loss. Inner ear therapies are emerging, genetic therapies are not so far for some diseases, and cochlear and other auditory implants afford efficient restoration of audition for severe to profoundly deaf people.

The main ambition of this Special Issue is to share the state-of-the-art in therapies for hearing loss, to scientists and physicians who are not so familiar with deafness.

Prof. Dr. Eric Truy
Guest Editor

Manuscript Submission Information

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Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2600 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • deafness
  • hearing loss
  • genetics
  • auditory implants
  • cochlear implants

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Published Papers (18 papers)

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15 pages, 1543 KiB  
Article
Speech Perception Changes in the Acoustically Aided, Nonimplanted Ear after Cochlear Implantation: A Multicenter Study
by Mario A. Svirsky, Arlene C. Neuman, Jonathan D. Neukam, Annette Lavender, Margaret K. Miller, Ksenia A. Aaron, Piotr H. Skarzynski, Katarzyna B. Cywka, Henryk Skarzynski, Eric Truy, Fabien Seldran, Ruben Hermann, Paul Govaerts, Geert De Ceulaer, Francois Bergeron, Matthieu Hotton, Michelle Moran, Richard C. Dowell, Maria Valeria Schmidt Goffi-Gomez, Ana Tereza de Matos Magalhães, Rosamaria Santarelli and Pietro Scimemiadd Show full author list remove Hide full author list
J. Clin. Med. 2020, 9(6), 1758; https://doi.org/10.3390/jcm9061758 - 5 Jun 2020
Cited by 2 | Viewed by 3340
Abstract
In recent years there has been an increasing percentage of cochlear implant (CI) users who have usable residual hearing in the contralateral, nonimplanted ear, typically aided by acoustic amplification. This raises the issue of the extent to which the signal presented through the [...] Read more.
In recent years there has been an increasing percentage of cochlear implant (CI) users who have usable residual hearing in the contralateral, nonimplanted ear, typically aided by acoustic amplification. This raises the issue of the extent to which the signal presented through the cochlear implant may influence how listeners process information in the acoustically stimulated ear. This multicenter retrospective study examined pre- to postoperative changes in speech perception in the nonimplanted ear, the implanted ear, and both together. Results in the latter two conditions showed the expected increases, but speech perception in the nonimplanted ear showed a modest yet meaningful decrease that could not be completely explained by changes in unaided thresholds, hearing aid malfunction, or several other demographic variables. Decreases in speech perception in the nonimplanted ear were more likely in individuals who had better levels of speech perception in the implanted ear, and in those who had better speech perception in the implanted than in the nonimplanted ear. This raises the possibility that, in some cases, bimodal listeners may rely on the higher quality signal provided by the implant and may disregard or even neglect the input provided by the nonimplanted ear. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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Figure 1
<p>Group mean of preoperative and average postoperative unaided thresholds.</p>
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<p>Postoperative vs. preoperative speech perception scores with the implanted ear only (left), both ears (bimodal condition, center), and the nonimplanted ear only (right). The top panels present average postoperative scores in the y-axis whereas the bottom panels show the latest available postoperative datapoint.</p>
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<p>Postoperative speech perception scores in the nonimplanted ear are lower than preoperative scores even after excluding subjects whose hearing aid functioning could not be verified, or after excluding datapoints from subjects who showed decreases in pure-tone average greater than 20, 20, or 5 dB. The top panel compares preoperative data to average postoperative data and the bottom panel compares it to the latest available postoperative data.</p>
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<p>Drop in postoperative speech perception scores in the nonimplanted ear as a function of: change in pure-tone average (left panel), implanted ear advantage (or degree to which speech perception is better in the implanted than in the nonimplanted ear, center panel), and speech perception score in the implanted ear (right panel).</p>
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15 pages, 1752 KiB  
Article
Biocompatibility of Bone Marrow-Derived Mesenchymal Stem Cells in the Rat Inner Ear following Trans-Tympanic Administration
by Adrien A. Eshraghi, Emre Ocak, Angela Zhu, Jeenu Mittal, Camron Davies, David Shahal, Erdogan Bulut, Rahul Sinha, Viraj Shah, Mario M. Perdomo and Rahul Mittal
J. Clin. Med. 2020, 9(6), 1711; https://doi.org/10.3390/jcm9061711 - 2 Jun 2020
Cited by 10 | Viewed by 3179
Abstract
Recent advancements in stem cell therapy have led to an increased interest within the auditory community in exploring the potential of mesenchymal stem cells (MSCs) in the treatment of inner ear disorders. However, the biocompatibility of MSCs with the inner ear, especially when [...] Read more.
Recent advancements in stem cell therapy have led to an increased interest within the auditory community in exploring the potential of mesenchymal stem cells (MSCs) in the treatment of inner ear disorders. However, the biocompatibility of MSCs with the inner ear, especially when delivered non-surgically and in the immunocompetent cochlea, is not completely understood. In this study, we determined the effect of intratympanic administration of rodent bone marrow MSCs (BM-MSCs) on the inner ear in an immunocompetent rat model. The administration of MSCs did not lead to the generation of any oxidative stress in the rat inner ear. There was no significant production of proinflammatory cytokines, tumor necrosis factor (TNF)-α, interleukin (IL)-1β, IL-6 and IL-12, due to BM-MSCs administration into the rat cochlea. BM-MSCs do not activate caspase 3 pathway, which plays a central role in sensory cell damage. Additionally, transferase dUTP nick end labeling (TUNEL) staining determined that there was no significant cell death associated with the administration of BM-MSCs. The results of the present study suggest that trans-tympanic administration of BM-MSCs does not result in oxidative stress or inflammatory response in the immunocompetent rat cochlea. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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Figure 1
<p>Oxidative stress determination: The levels of 8-isoprostane as a marker of oxidative stress was determined in whole cochlear tissue homogenates by ELISA at 3, 5, 7, 14, and 30 days post-administration. There was no statistically significant difference in 8-isoprostane levels in cochleae harvested from rats that received bone marrow mesenchymal stem cells (BM-MSCs), phosphate buffered saline (PBS) injected, or control group.</p>
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<p>Cleaved caspase 3 immunostaining: (<b>A</b>) Rat cochlear slices were subjected to cleaved caspase 3 immunostaining (red) to determine apoptosis. Cell nuclei were stained with DAPI (blue). Cochleae harvested from rats that received BM-MSCs, PBS injected, or control group showed no or sparse staining whereas those from the positive group showed intense staining (red color). Blue color shows DAPI staining. (<b>B</b>) Mean signal intensity for cleaved caspase 3 was calculated using Image J software. Data are expressed as mean values ± standard deviation (SD). WC: whole cochlea; SGNs: Spiral Ganglion Neurons; HCs: Hair Cells; SL: Spiral Ligament.</p>
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<p>Proinflammatory cytokines: The levels of proinflammatory cytokines, tumor necrosis factor (TNF)-α (<b>A</b>), interleukin (IL)-1β (<b>B</b>), IL-6 (<b>C</b>) and IL-12 (<b>D</b>) were determined in cochlear homogenates by ELISA. Data are expressed as mean values ± SD.</p>
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<p>Transferase dUTP nick end labeling (TUNEL) staining: Rat cochlear slices were subjected to TUNEL immunostaining to determine cell death. (<b>A</b>) Cochleae harvested from rats that received BM-MSCs, PBS injected, or control group showed no or sparse staining whereas those from positive group showed intense staining (red color). Blue color shows DAPI staining. (<b>B</b>) The percentage of TUNEL positive cells were calculated and graphed. Arrows indicate cell death in positive control group. WC: whole cochlea; SGNs: Spiral Ganglion Neurons; HCs: Hair Cells; SL: Spiral Ligament.</p>
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18 pages, 1190 KiB  
Article
Listening in Noise Remains a Significant Challenge for Cochlear Implant Users: Evidence from Early Deafened and Those with Progressive Hearing Loss Compared to Peers with Normal Hearing
by Yael Zaltz, Yossi Bugannim, Doreen Zechoval, Liat Kishon-Rabin and Ronen Perez
J. Clin. Med. 2020, 9(5), 1381; https://doi.org/10.3390/jcm9051381 - 8 May 2020
Cited by 27 | Viewed by 3955
Abstract
Cochlear implants (CIs) are the state-of-the-art therapy for individuals with severe to profound hearing loss, providing them with good functional hearing. Nevertheless, speech understanding in background noise remains a significant challenge. The purposes of this study were to: (1) conduct a novel within-study [...] Read more.
Cochlear implants (CIs) are the state-of-the-art therapy for individuals with severe to profound hearing loss, providing them with good functional hearing. Nevertheless, speech understanding in background noise remains a significant challenge. The purposes of this study were to: (1) conduct a novel within-study comparison of speech-in-noise performance across ages in different populations of CI and normal hearing (NH) listeners using an adaptive sentence-in-noise test, and (2) examine the relative contribution of sensory information and cognitive–linguistic factors to performance. Forty CI users (mean age 20 years) were divided into “early-implanted” <4 years (n = 16) and “late-implanted” >6 years (n = 11), all prelingually deafened, and “progressively deafened” (n = 13). The control group comprised 136 NH subjects (80 children, 56 adults). Testing included the Hebrew Matrix test, word recognition in quiet, and linguistic and cognitive tests. Results show poorer performance in noise for CI users across populations and ages compared to NH peers, and age at implantation and word recognition in quiet were found to be contributing factors. For those recognizing 50% or more of the words in quiet (n = 27), non-verbal intelligence and receptive vocabulary explained 63% of the variance in noise. This information helps delineate the relative contribution of top-down and bottom-up skills for speech recognition in noise and can help set expectations in CI counseling. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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Figure 1
<p>Individual speech reception thresholds in noise (SRTn) of the Hebrew Matrix sentence-in-noise test (mean signal-to-noise ratio (SNR) in measurements 3, 4) for early-implanted cochlear implants (CI) users (<span class="html-italic">n</span> = 16, seven implanted before two years of age), progressive CI users (<span class="html-italic">n</span> = 13), late-implanted CI users (<span class="html-italic">n</span> = 11), and normal hearing (NH) controls (<span class="html-italic">n</span> = 136). Mean performance of the NH ±1 standard deviation is shown between the gray lines.</p>
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<p>Box-and-whisker plot of the SRTn of the Hebrew Matrix sentence-in-noise test (mean SNR in measurements 3, 4) for early-implanted CI users (<span class="html-italic">n</span> = 16), progressive CI users (<span class="html-italic">n</span> = 13), late-implanted CI users (<span class="html-italic">n</span> = 11), and NH controls (children: <span class="html-italic">n</span> = 80, adults: 56). Also shown are the individual results of the children (empty circles) and adult (empty triangles) CI users. Note that within the “early-implanted” CI group, the children were implanted before two years of age.</p>
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<p>Box-and-whisker plot of the results in the Hebrew Arthur Boothroyd (AB) consonant–vowel–consonant (CVC) words in quiet (HAB) test for the early-implanted (<span class="html-italic">n</span> = 16), progressive (<span class="html-italic">n</span> = 13), and late-implanted (<span class="html-italic">n</span> = 10) CI users.</p>
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<p>Individual results in the Hebrew CVC words in quiet (HAB) test versus SRTn of the Hebrew Matrix sentence-in-noise test (mean SNR in measurements 3, 4), for the early-implanted (<span class="html-italic">n</span> = 16), progressive (<span class="html-italic">n</span> = 13), and late-implanted (<span class="html-italic">n</span> = 10) CI users.</p>
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<p>Individual scores in the (<b>a</b>) phonemic and (<b>b</b>) semantic fluency tests for the Q50 performers (CI users who scored ≥50% in the words-in-quiet test) compared to NH performance (shown between the broken lines: mean ± Standard deviation by age) from Kave and Knafo-Noam [<a href="#B72-jcm-09-01381" class="html-bibr">72</a>].</p>
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12 pages, 1868 KiB  
Article
Evaluating the Efficacy of L-N-acetylcysteine and Dexamethasone in Combination to Provide Otoprotection for Electrode Insertion Trauma
by Adrien A. Eshraghi, David Shahal, Camron Davies, Jeenu Mittal, Viraj Shah, Erdogan Bulut, Carolyn Garnham, Priyanka Sinha, Dibyanshi Mishra, Hannah Marwede and Rahul Mittal
J. Clin. Med. 2020, 9(3), 716; https://doi.org/10.3390/jcm9030716 - 6 Mar 2020
Cited by 6 | Viewed by 3552
Abstract
Background: Electrode insertion trauma (EIT) during cochlear implantation (CI) can cause loss of residual hearing. L-N-acetylcysteine (L-NAC) and dexamethasone (Dex) have been individually shown to provide otoprotection albeit at higher concentrations that may be associated with adverse effects. Objective/Aims: The aim of this [...] Read more.
Background: Electrode insertion trauma (EIT) during cochlear implantation (CI) can cause loss of residual hearing. L-N-acetylcysteine (L-NAC) and dexamethasone (Dex) have been individually shown to provide otoprotection albeit at higher concentrations that may be associated with adverse effects. Objective/Aims: The aim of this study is to determine whether L-NAC and Dex could be combined to decrease their effective dosage. Materials and Methods: The organ of Corti (OC) explants were divided into various groups: 1) control; 2) EIT; 3) EIT treated with different concentrations of Dex; 4) EIT treated with different concentrations of L-NAC; 5) EIT treated with L-NAC and Dex in combination. Hair cell (HC) density, levels of oxidative stress, proinflammatory cytokines and nitric oxide (NO) was determined. Results: There was a significant loss of HCs in explants subjected to EIT compared to the control group. L-NAC and Dex in combination was able to provide significant otoprotection at lower concentrations compared to individual drugs. Conclusions and Significance: A combination containing L-NAC and Dex is effective in protecting sensory cells at lower protective doses than each compound separately. These compounds can be combined allowing a decrease of potential side effects of each compound and providing significant otoprotection for EIT. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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Figure 1
<p>L-N-acetylcysteine (L-NAC) and dexamethasone (Dex) provides otoprotection against electrode insertion trauma (EIT). Organ of Corti (OC) explants were exposed to EIT alone or EIT and treated with L-NAC and Dex either individually or in combination. Samples were subjected to FITC-phalloidin staining to visualize hair cells (HCs). Results are representative of four independent experiments. Image represents middle + base area of explant. <span class="html-italic">n</span> = 9 OCs per group per experiment. Scale bars: 10 micrometers.</p>
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<p>Hair cell quantification. Total hair cells (THCs) were counted based on FITC-phalloidin staining. EIT-exposed OC explants showed a significant decrease in the number of THC compared to control group. L-NAC and Dex in combination was able to significantly prevent EIT induced sensory cell loss at lower doses. Data are expressed as mean values ± SD and are representative of four independent experiments. * <span class="html-italic">P</span> &lt; 0.05 or ** <span class="html-italic">P</span> &lt; 0.001 compared to EIT group. <span class="html-italic">n</span> = 9 OCs per group per experiment.</p>
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<p>Oxidative stress in OC explants. Mean signal intensity for CellROX was calculated using Image J software. Data are expressed as mean values ± SD and is representative of four independent experiments. * <span class="html-italic">P</span> &lt; 0.05 or ** <span class="html-italic">P</span> &lt; 0.001 compared to EIT group. <span class="html-italic">n</span> = 9 OCs per group per experiment.</p>
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<p>Proinflammatory cytokines. The levels of TNF-α (<b>A</b>), IL-1β (<b>B</b>), and IL-6 (<b>C</b>) were determined in OC homogenates using ELISA kits. Data are expressed as mean values ± SD and are representative of four independent experiments. * <span class="html-italic">P</span> &lt; 0.01 or ** <span class="html-italic">P</span> &lt; 0.001 compared to EIT group. <span class="html-italic">n</span> = 9 OCs per group per experiment.</p>
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<p>Nitric oxide (NO) levels in OC explants: NO production was determined in homogenates of OC explants. Data are expressed as mean values ± SD and are representative of three independent experiments. * <span class="html-italic">P</span> &lt; 0.01 or ** <span class="html-italic">P</span> &lt; 0.001 compared to EIT group. <span class="html-italic">n</span> = 9 OCs per group per experiment.</p>
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23 pages, 481 KiB  
Article
The Effect of Hearing Aid Use on Cognition in Older Adults: Can We Delay Decline or Even Improve Cognitive Function?
by Julia Sarant, David Harris, Peter Busby, Paul Maruff, Adrian Schembri, Ulrike Lemke and Stefan Launer
J. Clin. Med. 2020, 9(1), 254; https://doi.org/10.3390/jcm9010254 - 17 Jan 2020
Cited by 89 | Viewed by 39709
Abstract
Hearing loss is a modifiable risk factor for dementia in older adults. Whether hearing aid use can delay the onset of cognitive decline is unknown. Participants in this study (aged 62–82 years) were assessed before and 18 months after hearing aid fitting on [...] Read more.
Hearing loss is a modifiable risk factor for dementia in older adults. Whether hearing aid use can delay the onset of cognitive decline is unknown. Participants in this study (aged 62–82 years) were assessed before and 18 months after hearing aid fitting on hearing, cognitive function, speech perception, quality of life, physical activity, loneliness, isolation, mood, and medical health. At baseline, multiple linear regression showed hearing loss and age predicted significantly poorer executive function performance, while tertiary education predicted significantly higher executive function and visual learning performance. At 18 months after hearing aid fitting, speech perception in quiet, self-reported listening disability and quality of life had significantly improved. Group mean scores across the cognitive test battery showed no significant decline, and executive function significantly improved. Reliable Change Index scores also showed either clinically significant improvement or stability in executive function for 97.3% of participants, and for females for working memory, visual attention and visual learning. Relative stability and clinically and statistically significant improvement in cognition were seen in this participant group after 18 months of hearing aid use, suggesting that treatment of hearing loss with hearing aids may delay cognitive decline. Given the small sample size, further follow up is required. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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Figure 1
<p>Executive function (GML) raw scores at baseline and 18 month assessments and their pairwise differences. The Y axis shows the number of errors in responses. The X axis shows assessment points and the difference in scores between the baseline and 18 month post-hearing aid fitting assessments. The boxes represent the observations between the first and third quartile. The hollow circles represent outliers. The bolded lines in the boxes represent the medians.</p>
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11 pages, 1298 KiB  
Article
Cochlear Implantation Outcome in Children with DFNB1 locus Pathogenic Variants
by Dominika Oziębło, Anita Obrycka, Artur Lorens, Henryk Skarżyński and Monika Ołdak
J. Clin. Med. 2020, 9(1), 228; https://doi.org/10.3390/jcm9010228 - 15 Jan 2020
Cited by 12 | Viewed by 2919
Abstract
Almost 60% of children with profound prelingual hearing loss (HL) have a genetic determinant of deafness, most frequently two DFNB1 locus (GJB2/GJB6 genes) recessive pathogenic variants. Only few studies combine HL etiology with cochlear implantation (CI) outcome. Patients with profound prelingual HL [...] Read more.
Almost 60% of children with profound prelingual hearing loss (HL) have a genetic determinant of deafness, most frequently two DFNB1 locus (GJB2/GJB6 genes) recessive pathogenic variants. Only few studies combine HL etiology with cochlear implantation (CI) outcome. Patients with profound prelingual HL who received a cochlear implant before 24 months of age and had completed DFNB1 genetic testing were enrolled in the study (n = 196). LittlEARS questionnaire scores were used to assess auditory development. Our data show that children with DFNB1-related HL (n = 149) had good outcome from the CI (6.85, 22.24, and 28 scores at 0, 5, and 9 months post-CI, respectively). A better auditory development was achieved in patients who receive cochlear implants before 12 months of age. Children without residual hearing presented a higher rate of auditory development than children with responses in hearing aids over a wide frequency range prior to CI, but both groups reached a similar level of auditory development after 9 months post-CI. Our data shed light upon the benefits of CI in the homogenous group of patients with HL due to DFNB1 locus pathogenic variants and clearly demonstrate that very early CI is the most effective treatment method in this group of patients. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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Figure 1
<p>LEAQ scores at the time of cochlear implant activation. (<b>A</b>) Differences in LEAQ scores in patients with and without DFNB1 <span class="html-italic">locus</span> pathogenic variants; (<b>B</b>) differences in LEAQ scores in patients with minimal and wide responses provided by HAs; (<b>C</b>) differences in LEAQ scores in patients with very early and early CI. Whiskers represent 5–95 percentile, and black dots indicate outliers. Asterisks represent statistical significance, ***<span class="html-italic">p</span> &lt; 0.001; ns, not significant.</p>
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<p>Distribution of LEAQ scores at the time of cochlear implant activation in DFNB1 HL patients.</p>
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<p>LEAQ scores in the fifth month after cochlear implantation. (<b>A</b>) Differences in LEAQ scores in patients with and without DFNB1 <span class="html-italic">locus</span> pathogenic variants; (<b>B</b>) differences in LEAQ scores in patients with minimal and wide responses provided by HAs; (<b>C</b>) differences in LEAQ scores in patients with very early and early CI. Whiskers represent 5–95 percentile and black dots indicate outliers. Asterisks represent statistical significance, * <span class="html-italic">p</span> &lt; 0.05; ns, not significant.</p>
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<p>Distribution of LEAQ scores in the fifth month after CI in DFNB1 HL patients.</p>
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<p>Distribution of an average LEAQ score of patients with DFNB1 HL at subsequent time intervals (mean ± 95% confidence interval). Asterisks indicate statistically significant differences observed between patients with minimal HAs responses and very early CI vs. patients with wide HAs responses and early CI. Asterisks represent statistical significance, * <span class="html-italic">p</span> &lt; 0.05, *** <span class="html-italic">p</span> &lt; 0.001.</p>
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8 pages, 1365 KiB  
Article
Beware of a Fragile Footplate: Lessons from Ossiculoplasty in Patients with Ossicular Anomalies Related to Second Pharyngeal Arch Defects
by Sun A Han, Goun Choe, Yoonjoong Kim, Ja-Won Koo, Byung Yoon Choi and Jae-Jin Song
J. Clin. Med. 2019, 8(12), 2130; https://doi.org/10.3390/jcm8122130 - 3 Dec 2019
Cited by 8 | Viewed by 7922
Abstract
Background and objectives: We review the intraoperative findings and postoperative outcomes of ossiculoplasty in subjects with second pharyngeal arch (SPA)-derived ossicular anomalies. We summarize potential intraoperative complications and recommend precautions that may reduce the risk of fracture. Materials and Methods: Twenty-four patients with [...] Read more.
Background and objectives: We review the intraoperative findings and postoperative outcomes of ossiculoplasty in subjects with second pharyngeal arch (SPA)-derived ossicular anomalies. We summarize potential intraoperative complications and recommend precautions that may reduce the risk of fracture. Materials and Methods: Twenty-four patients with SPA-derived ossicular anomalies were included, and pre- and postoperative audiometric results were compared. Results: The mean air conduction threshold (56.0 ± 12.4 dB HL) was significantly improved 1 month (27.6 ± 10.1 dB HL) and 6 months (23.8 ± 13.2 dB HL) after surgery (p < 0.001). The preoperative air–bone gap (ABG) (40.4 ± 7.4 dB HL) was significantly decreased at 1 month (15.1 ± 5.9 dB HL) and 6 months (11.3 ± 8.9 dB HL) postoperation. ABG closure was successful (<20 dB HL) in 21 (87.5%) patients 6 months after surgery. Intraoperative footplate fractures occurred in 3 of 24 patients. The fractures were managed successfully, and the ABG closure was successful in all cases. Conclusions: The stapes footplate is likely to be relatively thin in subjects with SPA-derived ossicular anomalies because the footplate is partially or totally derived from the SPA. Thus, a fragile footplate should be expected, and care is needed when handling the footplate. However, when complications are overcome, the audiological outcomes are excellent in most cases. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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Graphical abstract

Graphical abstract
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<p>(<b>A</b>) Schematic representation of the ossicular chain; (<b>B</b>) Diagrammatic illustration of the theory suggesting that the medial portion of the footplate is derived from the otic capsule, while the lateral portion is derived from the second pharyngeal arch; (<b>C</b>) Diagrammatic illustration of the theory suggesting that the footplate is derived solely from the second pharyngeal arch. PA: pharyngeal arch.</p>
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<p>Changes in audiometric parameters after surgery. (<b>A</b>) Air conduction (AC) pure-tone average (PTA); (<b>B</b>) Bone conduction (BC) PTA; (<b>C</b>) Air–bone (AB) gap. * <span class="html-italic">p</span> values less than 0.05; Pre-op: preoperative average; 1mo: 1-month postoperative average; 6mo: 6-month postoperative average.</p>
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<p>Comparison of preoperative (preop) and postoperative (postop) audiometric outcomes in patients with intraoperative complications. (<b>A</b>) Case 1, a 42-year-old male; (<b>B</b>) Case 2, a 35-year-old male; (<b>C</b>) Case 3, a 61-year-old female. BC: bone conduction; AC: air conduction.</p>
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<p>The stapes footplate is (<b>A</b>) partially or (<b>B</b>) totally derived from the second PA.</p>
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17 pages, 2030 KiB  
Article
Solid Lipid Nanoparticles Loaded with Glucocorticoids Protect Auditory Cells from Cisplatin-Induced Ototoxicity
by Blanca Cervantes, Lide Arana, Silvia Murillo-Cuesta, Marina Bruno, Itziar Alkorta and Isabel Varela-Nieto
J. Clin. Med. 2019, 8(9), 1464; https://doi.org/10.3390/jcm8091464 - 14 Sep 2019
Cited by 38 | Viewed by 4991
Abstract
Cisplatin is a chemotherapeutic agent that causes the irreversible death of auditory sensory cells, leading to hearing loss. Local administration of cytoprotective drugs is a potentially better option co-therapy for cisplatin, but there are strong limitations due to the difficulty of accessing the [...] Read more.
Cisplatin is a chemotherapeutic agent that causes the irreversible death of auditory sensory cells, leading to hearing loss. Local administration of cytoprotective drugs is a potentially better option co-therapy for cisplatin, but there are strong limitations due to the difficulty of accessing the inner ear. The use of nanocarriers for the efficient delivery of drugs to auditory cells is a novel approach for this problem. Solid lipid nanoparticles (SLNs) are biodegradable and biocompatible nanocarriers with low solubility in aqueous media. We show here that stearic acid-based SLNs have the adequate particle size, polydispersity index and ζ-potential, to be considered optimal nanocarriers for drug delivery. Stearic acid-based SLNs were loaded with the fluorescent probe rhodamine to show that they are efficiently incorporated by auditory HEI-OC1 (House Ear Institute-Organ of Corti 1) cells. SLNs were not ototoxic over a wide dose range. Glucocorticoids are used to decrease cisplatin-induced ototoxicity. Therefore, to test SLNs’ drug delivery efficiency, dexamethasone and hydrocortisone were tested either alone or loaded into SLNs and tested in a cisplatin-induced ototoxicity in vitro assay. Our results indicate that the encapsulation in SLNs increases the protective effect of low doses of hydrocortisone and lengthens the survival of HEI-OC1 cells treated with cisplatin. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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Graphical abstract

Graphical abstract
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<p>Particle size, polydispersity index and ζ-potential of solid lipid nanoparticles (SLNs). (<b>A</b>) Particle size, (<b>B</b>) polydispersity index (pdi) and (<b>C</b>) ζ-potential values of different SLN suspensions: empty SLNs (SLN), SLNs loaded with rhodamine (SLN–RHO), SLNs loaded with dexamethasone (SLN–DEX) and SLNs loaded with hydrocortisone (SLN–HC). Data are shown as the mean ± SEM from five independent experiments.</p>
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<p>Uptake of SLN–RHO into HEI-OC1 cells. (<b>A</b>) HEI-OC1 cells were incubated with 250 µg/mL of rhodamine-loaded SLN (SLN–RHO). Fluorescence intensity of incorporated SLN–RHO was detected by confocal microscopy at the times indicated. Representative microphotographs from three independent experiments are shown. (<b>B</b>) HEI-OC1 cells were incubated with SLN–RHO (250 µg/mL) for different times, cells were then collected, and the fluorescent intensity of incorporated SLN–RHO was detected by flow cytometry. The plots shown are representative of three independent experiments, whose quantification is shown in (<b>C</b>). Data are shown as the mean ± SEM from three independent experiments. One-way ANOVA was used to determine statistical significance; ***<span class="html-italic">p</span> &lt; 0.001.</p>
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<p>The cytotoxicity of SLN–RHO and SLN in HEI-OC1 cells. (<b>A</b>) Flow cytometry analysis of cell cycle phase distribution in HEI-OC1 cells. Representative profiles of DAPI staining from control (no SLN) and SLN–RHO (250 µg/mL) treated cell cultures, at 0 h (<b>A</b>) and 20 h (<b>B</b>). (<b>C</b>) Histogram showing the cell distribution in the sub-G0/G1, G0/G1, S and G2/M phases in control and SLN–RHO (250 µg/mL) treated-cells. (<b>D</b>) HEI-OC1 cells were incubated or not with SLN–RHO for 20 h, stained with FITC-conjugated Annexin V and PI, and the pencentages of cell populations in early and late apoptosis were quantified. Data are shown as the mean ± SEM from three independent experiments. The significance of the differences was evaluated using Student´ <span class="html-italic">t</span> tests; *<span class="html-italic">p</span> &lt; 0.05 versus control condition (without SLNs). (<b>E</b>) HEI-OC1 cells were seeded into 96-well microplates 1500 cells/well and treated with the doses indicated of SLN for 24 h. Cell viability was determined with the Cell Proliferation Kit II (XTT) assay. Results are the mean ± SEM of two-three independent experiments performed in quadruplicate. The significance of the differences was evaluated using one-way ANOVA testing; * <span class="html-italic">p</span>  &lt;  0.05.</p>
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<p>Differential effects of free versus SLN-incorporated glucocorticoids on HEI-OC1 viability. Cell viability of HEI-OC1 treated with different concentrations of dexamethasone ((<b>A</b>), grey or pale green), hydrocortisone ((<b>B</b>), grey or pale blue), SLN–DEX ((<b>C</b>), dark green) or SLN–HC ((<b>D</b>), dark blue) over 24 h. The a and b green and blue bars also correspond to the doses tested for dexamethasone or hydrocortisone incorporated into SLN in (<b>C</b>) and (<b>D</b>), respectively. Cell viability was analyzed using the XTT assay as described in the Methods section. Results are shown as mean ± SEM. (<b>A</b>–<b>B</b>) data were obtained from two independent experiments performed in quadruplicate, whereas (<b>C</b>–<b>D</b>) data were obtained from two-four independent experiments performed in quadruplicate. The significance of the differences was evaluated using one-way ANOVA testing; ***<span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Comparative effects of SLN–DEX and dexamethasone on HEI-OC1 cells’ viability. Cell viability was evaluated by Cell Proliferation Kit II (XTT) assay. HEI-OC1 cells were treated for 24 h (<b>A</b>) or 48 h (<b>B</b>) with different concentrations of dexamethasone (DEX) either alone or combined with SLNs (SLN–DEX) in the absence or presence of 2 or 4 µg/mL cisplatin. Results are shown as mean ± SEM from four independent experiments. The significance of the differences was evaluated using one-way ANOVA testing; ***<span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Comparative effects of SLN–HC and hydrocortisone on HEI-OC1 cell viability. Cell viability was evaluated by Cell Proliferation kit II (XTT) assay. HEI-OC1 cells were treated for 24 h (<b>A</b>) or 48 h (<b>B</b>) with different concentrations of hydrocortisone (HC) either alone or combined with SLNs (SLN–HC) in the absence or presence of 2 or 4 µg/mL cisplatin. Results are shown as mean ± SEM from four independent experiments. The significance of the differences was evaluated using one-way ANOVA testing, ***<span class="html-italic">p</span> &lt; 0.001.</p>
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12 pages, 890 KiB  
Article
“Third Window” and “Single Window” Effects Impede Surgical Success: Analysis of Retrofenestral Otosclerosis Involving the Internal Auditory Canal or Round Window
by Yun Jung Bae, Ye Ji Shim, Byung Se Choi, Jae-Hyoung Kim, Ja-Won Koo and Jae-Jin Song
J. Clin. Med. 2019, 8(8), 1182; https://doi.org/10.3390/jcm8081182 - 7 Aug 2019
Cited by 10 | Viewed by 4753
Abstract
Background and Objectives: We aimed to identify prognostic computed tomography (CT) findings in retrofenestral otosclerosis, with particular attention paid to the role of otosclerotic lesion area in predicting post-stapedotomy outcome. Materials and Methods: We included 17 subjects (23 ears) with retrofenestral otosclerosis who [...] Read more.
Background and Objectives: We aimed to identify prognostic computed tomography (CT) findings in retrofenestral otosclerosis, with particular attention paid to the role of otosclerotic lesion area in predicting post-stapedotomy outcome. Materials and Methods: We included 17 subjects (23 ears) with retrofenestral otosclerosis who underwent stapedotomy. On preoperative CT, the presence of cavitating lesion and involvement of various subsites (cochlea, round window [RW], vestibule, and semicircular canal) were assessed. Pre- and post-stapedotomy audiometric results were compared according to the CT findings. The surgical outcomes were analyzed using logistic regression with Firth correction. Results: Cavitating lesions were present in 15 of 23 ears (65.2%). Involvement of the RW was the strongest predictor of unsuccessful surgical outcome, followed by involvement of the internal auditory canal (IAC) and the cochlea. Conclusions: RW and IAC involvement in retrofenestral otosclerosis were shown to predict unsuccessful outcomes. While a “third window” effect caused by extension of a cavitating lesion into the IAC may dissipate sound energy and thus serve as a barrier to desirable postoperative audiological outcome, a “single window” effect due to an extension of retrofenestral otosclerosis into the RW may preclude a good surgical outcome, even after successful stapedotomy, due to less compressible cochlear fluid and thus decreased linear movement of the piston. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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<p>(<b>A</b>) Axial computed tomography (CT) image showing the presence of a focal hypodense notch connecting to the anterior wall of the internal auditory canal (IAC), designated as a cavitating lesion with IAC involvement (arrow). (<b>B</b>) Axial CT image showing otosclerotic involvement of the cochlear (black arrow) and the vestibule (white arrow). (<b>C</b>,<b>D</b>) Axial CT images showing retrofenestral involvement of the (<b>C</b>) round window and (<b>D</b>) the lateral semicircular canal (arrows). (<b>E</b>) Confluence between the cavitating lesion involving the IAC and cochlear involvement was demonstrated on axial CT (arrows).</p>
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<p>(<b>A</b>) Restoration of air conduction (AC) energy and near-normalized sound conduction in a subject with otosclerosis after stapedotomy. (<b>B</b>) Even after restoration of AC energy at the level of the footplate of the stapes by successful stapedotomy, shunting across the cavitating lesion to the internal auditory canal may play a role in dissipating sound energy, thus serving as a barrier to desirable postoperative audiological outcomes. (<b>C</b>) Decreased compliance of the round window due to otosclerosis involvement may result in increased mechanical load on the footplate, reduced volume velocity of the stapes, and thus decreased ossicular coupling presenting as increased air-bone gap. Adapted with permission from Rosowski, J.J. Conductive hearing loss caused by third window lesions of the inner ear [<a href="#B41-jcm-08-01182" class="html-bibr">41</a>].</p>
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Review

Jump to: Research, Other

27 pages, 3658 KiB  
Review
Inner Ear Gene Therapies Take Off: Current Promises and Future Challenges
by Sedigheh Delmaghani and Aziz El-Amraoui
J. Clin. Med. 2020, 9(7), 2309; https://doi.org/10.3390/jcm9072309 - 21 Jul 2020
Cited by 79 | Viewed by 12223
Abstract
Hearing impairment is the most frequent sensory deficit in humans of all age groups, from children (1/500) to the elderly (more than 50% of the over-75 s). Over 50% of congenital deafness are hereditary in nature. The other major causes of deafness, which [...] Read more.
Hearing impairment is the most frequent sensory deficit in humans of all age groups, from children (1/500) to the elderly (more than 50% of the over-75 s). Over 50% of congenital deafness are hereditary in nature. The other major causes of deafness, which also may have genetic predisposition, are aging, acoustic trauma, ototoxic drugs such as aminoglycosides, and noise exposure. Over the last two decades, the study of inherited deafness forms and related animal models has been instrumental in deciphering the molecular, cellular, and physiological mechanisms of disease. However, there is still no curative treatment for sensorineural deafness. Hearing loss is currently palliated by rehabilitation methods: conventional hearing aids, and for more severe forms, cochlear implants. Efforts are continuing to improve these devices to help users to understand speech in noisy environments and to appreciate music. However, neither approach can mediate a full recovery of hearing sensitivity and/or restoration of the native inner ear sensory epithelia. New therapeutic approaches based on gene transfer and gene editing tools are being developed in animal models. In this review, we focus on the successful restoration of auditory and vestibular functions in certain inner ear conditions, paving the way for future clinical applications. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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<p>Mammalian inner ear anatomy and cochlear tonotopic organization. The mammalian inner ear consists of the vestibule (balance organs), which detect linear and angular accelerations, and the cochlea, the hearing organ, which detects sound waves. (<b>A</b>,<b>B</b>) The cochlea is made up of three fluid-filled compartments of differing ionic compositions—<span class="html-italic">scala vestibuli</span> (perilymph), the <span class="html-italic">scala media</span> (endolymph), and the <span class="html-italic">scala tympani</span> (perilymph). Sound conversion into electrical signals requires three major types of functional cells: hair cells (purple), supporting cells, and spiral ganglion neurons (yellow). (<b>C</b>) The auditory sensory organ, the organ of Corti, is made up of one row of highly organized inner hair cells (IHCs), three rows of outer hair cells (OHCs), flanked by various types of supporting cells. Along the cochlea, the hair cells, underlying basilar membrane (BM), surrounding, and overlying tectorial membrane (TM) are optimized to perceive specific and characteristic sound frequencies, defining a cochlear tonotopy that is preserved up to the auditory cortex. The structural and physical properties of the cochlea vary from base (shorter and stiffer cells) to apex (longer and more flexible cells). The cochlear base mainly perceives high-frequency tones (up to 20 kHz in humans), while the apex detects low-frequency sounds (20 Hz in humans). Scale bar in B, C: 1 μm.</p>
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<p>Hearing loss causal origins and adapted therapeutic strategies. (<b>A</b>) Hearing loss, defined as mild (loss of 21 to 40 dB HL), moderate (41–70 dB HL loss), severe (71–90 dB HL loss), or profound (&gt;90 dB HL loss), can be due to multiple causes: genetic, noise, and/or age. Whatever the cause, the hearing loss can start any time after birth, with varying degrees of progression and severity. (<b>B</b>) Various therapeutic approaches (gene supplementation, silencing, or gene editing) are being implemented either to protect, prevent and/or repair hearing loss, regenerate or replace inner ear cells.</p>
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<p>Functional stratification genes/proteins causing human isolated deafness hearing loss. Based on their established role and characterization of corresponding animal models, the human deafness genes (<span class="html-italic">DFNA DFNB DFNX AUNA</span>) can be grouped into several functional categories: (1) hair bundle development and functioning, (2) synaptic transmission, (3) hair cell’s adhesion and maintenance, (4) cochlea ion homeostasis, (5) transmembrane or secreted proteins and extracellular matrix, (6) oxidative stress, metabolism and mitochondrial defects, and (7) transcriptional regulation. DFNAi (red) denotes autosomal-dominant forms of deafness with undefined locus number. The genes/loci in grey denote that they share several functional categories. More detailed information regarding the deafness causative genes are provided in <a href="#app1-jcm-09-02309" class="html-app">Table S1</a>.</p>
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<p>Delivery approaches in the inner ear. Schematic representation of the human ear, illustrating methods used to deliver therapeutics into the inner ear. These include systemic (red) and middle ear (blue) indirect approaches, as well as endolymphatic sac delivery (light blue) and direct injections through different compartments of the inner ear (green): cochleostomy (<span class="html-italic">scala media</span>), vestibule (through utricle or semicircular canal), and cochlea (through round window membrane or oval window). Some pros and cons of each methods are highlighted in <a href="#app1-jcm-09-02309" class="html-app">Table S2</a>.</p>
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29 pages, 6016 KiB  
Review
Auditory Neuropathy Spectrum Disorders: From Diagnosis to Treatment: Literature Review and Case Reports
by Romolo Daniele De Siati, Flora Rosenzweig, Guillaume Gersdorff, Anaïs Gregoire, Philippe Rombaux and Naïma Deggouj
J. Clin. Med. 2020, 9(4), 1074; https://doi.org/10.3390/jcm9041074 - 10 Apr 2020
Cited by 54 | Viewed by 16852
Abstract
Auditory neuropathy spectrum disorder (ANSD) refers to a range of hearing impairments characterized by deteriorated speech perception, despite relatively preserved pure-tone detection thresholds. Affected individuals usually present with abnormal auditory brainstem responses (ABRs), but normal otoacoustic emissions (OAEs). These electrophysiological characteristics have led [...] Read more.
Auditory neuropathy spectrum disorder (ANSD) refers to a range of hearing impairments characterized by deteriorated speech perception, despite relatively preserved pure-tone detection thresholds. Affected individuals usually present with abnormal auditory brainstem responses (ABRs), but normal otoacoustic emissions (OAEs). These electrophysiological characteristics have led to the hypothesis that ANSD may be caused by various dysfunctions at the cochlear inner hair cell (IHC) and spiral ganglion neuron (SGN) levels, while the activity of outer hair cells (OHCs) is preserved, resulting in discrepancies between pure-tone and speech comprehension thresholds. The exact prevalence of ANSD remains unknown; clinical findings show a large variability among subjects with hearing impairment ranging from mild to profound hearing loss. A wide range of prenatal and postnatal etiologies have been proposed. The study of genetics and of the implicated sites of lesion correlated with clinical findings have also led to a better understanding of the molecular mechanisms underlying the various forms of ANSD, and may guide clinicians in better screening, assessment and treatment of ANSD patients. Besides OAEs and ABRs, audiological assessment includes stapedial reflex measurements, supraliminal psychoacoustic tests, electrocochleography (ECochG), auditory steady-state responses (ASSRs) and cortical auditory evoked potentials (CAEPs). Hearing aids are indicated in the treatment of ANSD with mild to moderate hearing loss, whereas cochlear implantation is the first choice of treatment in case of profound hearing loss, especially in case of IHC presynaptic disorders, or in case of poor auditory outcomes with conventional hearing aids. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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<p>Audiological assessment in a 5-year-old child with auditory neuropathy spectrum disorder (ANSD) caused by neonatal hypoxia. Poor unaided pure-tone perception (<b>a</b>, gray line) was restored with hearing aids ((<b>a</b>), black line). Panel (<b>b</b>) displays auditory brainstem responses (ABRs) evoked by clicks presented in rarefaction (R) and condensation (C) polarities and the subtraction and summation of R and C (R − C and R + C, respectively), showing detectable cochlear microphonic (CM) and absence of waves V. Electrocochleography (ECochG) recorded through a transtympanic electrode on the promontory wall using 1000 Hz tone burst presented in alternated R and C polarities at a rate of 14.3 s (<b>c</b>) shows a large summating potential (SP). Auditory steady-state responses (ASSRs) thresholds (<b>d</b>) are present in the left (X) more than in the right (O) ear.</p>
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<p>Audiological assessment in 8-year-old patient with CAPOS syndrome. CAPOS is an acronym for Cerebellar ataxia, Areflexia, Pes cavus, Optic atrophy and Sensorineural hearing loss. Unaided pure tonal thresholds in both ears are shown in (<b>a</b>). The tonal hearing thresholds remain poor in the right ear aided by an acoustical hearing aid ((<b>b</b>), gray line) but are clearly improved in the left ear by cochlear implant ((<b>b</b>), black line). Speech perception was poor in unaided condition ((<b>c</b>), 10% gray dot at 60dB), it was partially improved by acoustical hearing aids ((<b>c</b>), gray line) but became significantly better with cochlear implant ((<b>c</b>), black line). abnormal auditory brainstem responses (ABRs) (<b>d</b>) show the responses evoked by clicks presented in rarefaction (R) and condensation (C) phase and the subtraction of R and C (R − C), highlighting the cochlear microphonic (CM) and the lack of waves V in the summation (R + C). Auditory steady-state responses (ASSRs) thresholds (<b>e</b>) are present in the left (X) more than in the right (O) ear.</p>
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<p>Distribution of pure-tone audiometry threshold (<b>a</b>) and (when possible) speech audiometry threshold for disyllabic words (<b>b</b>) in 14 patients aged between 5 and 48 years with auditory neuropathy spectrum disorder (ANSD). Etiologies of ANSD vary among patients. The figure is intended to show the large variability in hearing ability among patients with ANSD.</p>
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<p>Audiological assessment in an adult patient with auditory neuropathy spectrum disorder (ANSD) and bilateral cochlear nerve atrophy. Unaided thresholds for pure-tone audiometry ((<b>a</b>), black line for right ear, gray line for left ear) and speech audiometry ((<b>b</b>), black line for right ear, gray line for left ear) in quiet are good. Otoacoustic emissions (OAEs) are present bilaterally in both temporal/intensity recordings (left panel in (<b>c</b>) for right ear, left panel in (<b>d</b>) for left ear) and spectral analysis (right panel in (<b>c</b>) for right ear, right panel in (<b>d</b>) for left ear); on the other hand, auditory brainstem responses (ABRs) are abnormal with no clear cochlear microphonic (CM) ((<b>e</b>) for right ear, (<b>f</b>) for left ear).</p>
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<p>Auditory brainstem responses (ABRs) in a 26-week preterm newborn with auditory neuropathy spectrum disorder (ANSD). Three-month ABRs (<b>a</b>) show small early components, whereas a cochlear microphonic (CM) was detectable 9 months later (<b>b</b>), suggesting a late, although partial, maturation. Auditory steady-state responses (ASSRs) remain absent in both ears.</p>
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<p>Audiological assessment in adult with acquired auditory neuropathy spectrum disorder (ANSD) caused by bilateral cochlear nerve hypotrophia of unknown etiology. Unaided pure tone ((<b>a</b>), black line for right ear, gray line for left ear) and speech ((<b>b</b>), both ears in free field) thresholds are poor, with no improvement with hearing aids. Electrocochleography (ECochG) recorded after clicks at 90 dB and at a rate of 14.3 s ((<b>c</b>), grand average, above; superimposed, below) shows preserved summating potential (SP) and compound action potential (CAP). ECochG responses to tone-burst stimuli at different frequencies ((<b>d</b>), grand averages for 8, 4, 3, 2 and 1 kHz) show a large SP. Auditory brainstem responses (ABRs) are absent, except for the cochlear microphonic (CM) (<b>e</b>). The 3-Tesla magnetic resonance imaging of the right ear without contrast (<b>f</b>) shows the hypoplasia of the cochlear nerve.</p>
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<p>Audiological assessment in a subject with Brown–Vialetto–Van Laere syndrome-related auditory neuropathy spectrum disorder (ANSD), resulting in neural impairment of the 8th and 12th cranial nerves and the optic nerves. Unaided pure-tone audiometry ((<b>a</b>), both ears) shows bilateral hearing loss mainly for low frequencies. Unaided free field speech discrimination is poor ((<b>b</b>), 10% gray dot at 80 dB). Aided tonal and speech perception outcomes with acoustical hearing aids remain poor and comparable to unaided perception. The latter clearly improves after cochlear implantation (CI) ((<b>b</b>)<b>,</b> black line). Otoacoustic emissions (OAEs) are present ((<b>c</b>), spectral analysis of OAEs in the white area, compared to noise in the black area), whereas auditory brainstem responses (ABRs) synchronization was abnormal with no wave V but a clear cochlear microphonic (CM) in both rarefaction (R) and condensation (C) polarities and in the subtraction R − C (<b>d</b>). Cortical auditory evoked responses (<b>e</b>) show a P3 complex after stimulation with an oddball paradigm and in selective attentive conditions only, even if no recordable N100 or P200 waves are present in responses to the frequent stimuli (not shown).</p>
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<p>Audiological assessment in a 14-year-old child with auditory neuropathy spectrum disorder (ANSD) features occurring with severe hearing loss. Her medical history includes a 35-week preterm birth after an intrahepatic cholestasis of pregnancy, with normal birth weight but neonatal hypoxia requiring 3 weeks of stay in neonatal intensive care unit. Hearing aids were fitted in early infancy. Besides poor sounds recognition and speech perception, speech development was good in the lexical and morphosyntactic fields. Unaided tonal thresholds ((<b>a</b>), gray line for right ear, black line for left ear) and unaided speech discrimination (<b>b</b>) are poor. Aided pure-tone audiometry (<b>c</b>) and speech perception (<b>d</b>) with hearing aids are clearly improved, allowing a good development of language skills and learning abilities. Auditory brainstem responses (ABRs) elicited by clicks at 90 dB show small cochlear microphonic (CM) (<b>e</b>). Auditory steady-state responses (ASSRs) (<b>f</b>) are detected for 500 Hz at the right ear.</p>
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<p>Audiological assessment in a 14-years-old male with auditory neuropathy spectrum disorder (ANSD). His medical history includes neonatal hyperbilirubinemia and low birth weight. Despite early hearing aids fitting, speech development was delayed. He shows residual pure-tone hearing thresholds ((<b>a</b>), gray line) and poor speech discrimination ((<b>b</b>), gray line) in the left ear. After left-ear cochlear implantation, aided tonal ((<b>a</b>), black line) and speech ((<b>b</b>), black line) thresholds show good auditory outcomes. Auditory brainstem responses (ABRs) at left ear are absent (<b>c</b>). However, speech perception in noise, such as during school activities, remains poor.</p>
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13 pages, 7265 KiB  
Review
Hearing with One Ear: Consequences and Treatments for Profound Unilateral Hearing Loss
by Hillary A. Snapp and Sebastian A. Ausili
J. Clin. Med. 2020, 9(4), 1010; https://doi.org/10.3390/jcm9041010 - 3 Apr 2020
Cited by 44 | Viewed by 10574
Abstract
There is an increasing global recognition of the negative impact of hearing loss, and its association to many chronic health conditions. The deficits and disabilities associated with profound unilateral hearing loss, however, continue to be under-recognized and lack public awareness. Profound unilateral hearing [...] Read more.
There is an increasing global recognition of the negative impact of hearing loss, and its association to many chronic health conditions. The deficits and disabilities associated with profound unilateral hearing loss, however, continue to be under-recognized and lack public awareness. Profound unilateral hearing loss significantly impairs spatial hearing abilities, which is reliant on the complex interaction of monaural and binaural hearing cues. Unilaterally deafened listeners lose access to critical binaural hearing cues. Consequently, this leads to a reduced ability to understand speech in competing noise and to localize sounds. The functional deficits of profound unilateral hearing loss have a substantial impact on socialization, learning and work productivity. In recognition of this, rehabilitative solutions such as the rerouting of signal and hearing implants are on the rise. This review focuses on the latest insights into the deficits of profound unilateral hearing impairment, and current treatment approaches. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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<p>(<b>A</b>) An illustration of the acoustic head-shadow and the principle of time-delay between the two ears, dependent on the sound source. (<b>B</b>) Right and left temporal signals arriving from a right-leading sound source location. The ILD and ITD are illustrated on the amplitude and temporal domains, respectively. (<b>C</b>) The frequency and azimuth dependencies of the head and pinnae filter are shown. As the sound source moves from the hearing side (positive azimuth angles) to the deaf side (negative azimuth angles), the acoustic barrier created by the head attenuates high frequency signals contralateral to the source. Pinna gains are also observed for some frequencies at the ear ipsilateral to the source. (<b>D</b>) An illustration of the monaural spectral-pinnae cues as a function of the vertical position (elevation) of the sound source. The black arrows indicate the position-dependent frequency notch.</p>
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<p>Comparison of the head-shadow and pinnae filtering for the words (<b>A</b>) <span class="html-italic">”Hat”</span> and (<b>B</b>) <span class="html-italic">“Sat”</span> when presented at the deaf side. Spectrograms and sound waveforms (in gray) of the speech stimuli are shown for five corresponding azimuth positions. High frequency speech components are attenuated on the hearing side, erasing the unique informational marks that differentiate the words from each other.</p>
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<p>An illustration of spatial hearing abilities for (<b>A</b>) normal hearing and (<b>B</b>) single-sided deaf listeners. Normal hearing listeners localize target sounds accurately and precisely along the horizontal (azimuth) and vertical (elevation) planes. Monaural hearing listeners, instead, can localize target sounds mainly in the hemifield of the hearing ear, with impaired performance on the contralateral deaf side.</p>
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<p>Actual treatment solutions for profound unilateral hearing loss. Rerouting devices transmit the captured sound on the deaf side to the hearing ear (monaural input). In contralateral routing of signal (CROS) hearing aids, the transmitter wirelessly communicates to the contralateral hearing aid. Bone conduction devices transfer the sounds via transcranial skull vibrations towards the functional cochlea. The cochlear implant provides electrical stimulation directly to the deaf ear, preserving the contralateral acoustic hearing (bilateral input).</p>
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20 pages, 1369 KiB  
Review
Research Insights on Neural Effects of Auditory Deprivation and Restoration in Unilateral Hearing Loss: A Systematic Review
by Jolijn Vanderauwera, Elisabeth Hellemans and Nicolas Verhaert
J. Clin. Med. 2020, 9(3), 812; https://doi.org/10.3390/jcm9030812 - 17 Mar 2020
Cited by 31 | Viewed by 6109
Abstract
Neuroplasticity following bilateral deafness and auditory restoration has been repeatedly investigated. In clinical practice, however, a significant number of patients present a severe-to-profound unilateral hearing loss (UHL). To date, less is known about the neuroplasticity following monaural hearing deprivation and auditory input restoration. [...] Read more.
Neuroplasticity following bilateral deafness and auditory restoration has been repeatedly investigated. In clinical practice, however, a significant number of patients present a severe-to-profound unilateral hearing loss (UHL). To date, less is known about the neuroplasticity following monaural hearing deprivation and auditory input restoration. This article provides an overview of the current research insights on the impact of UHL on the brain and the effect of auditory input restoration with a cochlear implant (CI). An exhaustive systematic review of the literature was performed selecting 38 studies that apply different neural analyses techniques. The main results show that the hearing ear becomes functionally dominant after monaural deprivation, reshaping the lateralization of the neural network for auditory processing, a process that can be considered to influence auditory restoration. Furthermore, animal models predict that the onset time of UHL impacts auditory restoration. Hence, the results seem to advocate for early restoration of UHL, although further research is required to disambiguate the effects of duration and onset of UHL on auditory restoration and on structural neuroplasticity following UHL deprivation and restoration. Ongoing developments on CI devices compatible with Magnetic Resonance Imaging (MRI) examinations will provide a unique opportunity to investigate structural and functional neuroplasticity following CI restoration more directly. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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<p>Overview of selection of relevant records according to the PRISMA guidelines (2009).</p>
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<p>Visualization of the MRI artefacts caused by a unilateral cochlear implant (CI). In the left panel, the midsagittal plane has been visualized, showing large artefacts around the temporal lobe, while the inter-hemispherical corpus callosum is not hampered. The right panel shows an axial slice with extensive MRI artefacts.</p>
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<p>MRI artefacts caused by a unilateral CI on a coronal slice at the level of the auditory cortex. On the hemisphere contralateral to the device, the primary auditory cortex (Heschl’s gyrus) is depicted in <span class="html-italic">green</span> and the secondary auditory cortex (planum temporale) in <span class="html-italic">orange</span>.</p>
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12 pages, 247 KiB  
Review
Does Treating Hearing Loss in Older Adults Improve Cognitive Outcomes? A Review
by Hélène Amieva and Camille Ouvrard
J. Clin. Med. 2020, 9(3), 805; https://doi.org/10.3390/jcm9030805 - 16 Mar 2020
Cited by 49 | Viewed by 8326
Abstract
Hearing loss is the third most prevalent health condition in older age. In recent years, research has consistently reported an association between hearing loss and mental health outcomes, including poorer cognitive performances. Whether treating hearing loss in elders improves cognition has been directly [...] Read more.
Hearing loss is the third most prevalent health condition in older age. In recent years, research has consistently reported an association between hearing loss and mental health outcomes, including poorer cognitive performances. Whether treating hearing loss in elders improves cognition has been directly or indirectly addressed by several studies. This review aims at providing a synthesis of those results. Regarding the literature on hearing aids’ use and cognition, although the lack of interventional studies has to be underlined, observational data suggest that hearing aids positively impact long-term cognition, even though more research is necessary to ascertain this statement and provide information on the length or frequency of use required in order to observe benefits. Regarding cochlear implants in elders experiencing more severe auditory deprivation, the literature is scarcer. The available studies have many limitations and do not allow the drawing of clear conclusions. Taken together, the results are encouraging. Nevertheless, because hearing loss is suspected to account for 9% of dementia cases, and also because hearing loss is one of the few potentially modifiable factors from a dementia prevention perspective, the need to stimulate research to have clearer knowledge of the benefits of treating hearing loss on cognitive outcomes is urgent. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
21 pages, 4157 KiB  
Review
rAAV-Mediated Cochlear Gene Therapy: Prospects and Challenges for Clinical Application
by Fabian Blanc, Michel Mondain, Alexis-Pierre Bemelmans, Corentin Affortit, Jean-Luc Puel and Jing Wang
J. Clin. Med. 2020, 9(2), 589; https://doi.org/10.3390/jcm9020589 - 21 Feb 2020
Cited by 13 | Viewed by 6809
Abstract
Over the last decade, pioneering molecular gene therapy for inner-ear disorders have achieved experimental hearing improvements after a single local or systemic injection of adeno-associated, virus-derived vectors (rAAV for recombinant AAV) encoding an extra copy of a normal gene, or ribozymes used to [...] Read more.
Over the last decade, pioneering molecular gene therapy for inner-ear disorders have achieved experimental hearing improvements after a single local or systemic injection of adeno-associated, virus-derived vectors (rAAV for recombinant AAV) encoding an extra copy of a normal gene, or ribozymes used to modify a genome. These results hold promise for treating congenital or later-onset hearing loss resulting from monogenic disorders with gene therapy approaches in patients. In this review, we summarize the current state of rAAV-mediated inner-ear gene therapies including the choice of vectors and delivery routes, and discuss the prospects and obstacles for the future development of efficient clinical rAAV-mediated cochlear gene medicine therapy. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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<p>Inner ear anatomy and barriers. <b>A:</b> A schematic drawing of the structures of middle and inner ears, and inner-ear fluid flow and barriers. The tympanic membrane (TM) separates the external auditory canal from the middle ear that communicates with the nasopharynx via the Eustachian tube. The ossicular chain links the TM to the oval window (OW). Both round window (RW) and OW membranes form the connection between the middle ear and the cochlear perilymphatic space. The yellow arrows indicate communications between the perilymphatic spaces of the inner ear and the surrounding structures. <b>B:</b> Cross section of a single cochlear turn. The cochlea is made up of three canals: scala vestibuli (SV) and scala tympani (ST), filled with perilymph (in white), and scala media (SM), filled with endolymph (in blue). The red box indicates the organ of Corti. <b>C:</b> Shown is the organ of Corti. The organ of Corti located on the basilar membrane (in pink) is composed of mechanosensory cells, with three rows of outer hair cells (OHC) and one row of inner hair cells (IHC). Separating these hair cells are supporting cells (SCs). The nerve fibers (shown in green, nf) of the spiral ganglion neurons connect to sensory hair cells.</p>
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<p>Schematic illustration of main administration routes tested in mice and potential suitable routes for human applications. The vectors can be delivered locally into the perilymph through the scala tympani (ST), trans-round-window (RW) membrane, or an oval-window (OW)/trans-stapedial injection into the endolymph through the scala media (SM) injection, canalostomy (C) or endolymphatic sac (ES) injection, and systemically through intravenous injection. The gray and white colors indicate the endolymphatic and perilymphatic spaces in the inner ear, respectively. The blue and green syringes indicate the main routes of administration tested in mice and the green and yellow syringes indicate the potential ones suitable for human applications. SV: scala vestibuli. Amp: ampulla.</p>
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22 pages, 2356 KiB  
Review
Presbycusis: An Update on Cochlear Mechanisms and Therapies
by Jing Wang and Jean-Luc Puel
J. Clin. Med. 2020, 9(1), 218; https://doi.org/10.3390/jcm9010218 - 14 Jan 2020
Cited by 132 | Viewed by 19592
Abstract
Age-related hearing impairment (ARHI), also referred to as presbycusis, is the most common sensory impairment seen in the elderly. As our cochlea, the peripheral organ of hearing, ages, we tend to experience a decline in hearing and are at greater risk of cochlear [...] Read more.
Age-related hearing impairment (ARHI), also referred to as presbycusis, is the most common sensory impairment seen in the elderly. As our cochlea, the peripheral organ of hearing, ages, we tend to experience a decline in hearing and are at greater risk of cochlear sensory-neural cell degeneration and exacerbated age-related hearing impairments, e.g., gradual hearing loss, deterioration in speech comprehension (especially in noisy environments), difficulty in the localization sound sources, and ringing sensations in the ears. However, the aging process does not affect people uniformly; nor, in fact, does the aging process appear to be uniform even within an individual. Here, we outline recent research into chronological cochlear age in healthy people, and exacerbated hearing impairments during aging due to both extrinsic factors including noise and ototoxic medication, and intrinsic factors such as genetic predisposition, epigenetic factors, and aging. We review our current understanding of molecular pathways mediating ARHL and discuss recent discoveries in experimental hearing restoration and future prospects. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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<p>Inner-ear anatomy. (<b>A</b>) Schematic representation of ear anatomy. The ear is divided into three parts (insert): the external and middle ear transfer the sound waves to the inner ear where they are transduced into neural activity. The external ear is closed off from the middle ear by the eardrum. In the middle ear, the eardrum is mechanically linked, by a chain of three tiny bones (the ossicles), to the oval-window membrane which closes the inner ear. Embedded in the temporal bone, the inner ear comprises the balance organ or vestibule, and the hearing organ or cochlea. (<b>B</b>) Scanning electron micrograph of the organ of Corti. The cochlea is a coiled organ that forms a spiral. Scanning electron micrographs show a narrow, linear shape of IHC stereocilial bundles and a V-shape of OHC stereocilia. (<b>C</b>) Transverse section of the basal cochlear turn under light microscopy. The cochlea is made up of three canals wrapped around a bony axis, the modiolus. These canals are the scala tympani (ST), the scala vestibuli (SV), and the scala media (SM). The ST and SV are filled with perilymph. The SM is filled with endolymph. The organ of Corti is situated on the basilar membrane (bm). (<b>B</b>) = 2 mm, (<b>C</b>) = 10 µM, (<b>D</b>) = 50 µm. IHCs: inner hair cells; OHCs: outer hair cells ((<b>B</b>–<b>D</b>) micrographs courtesy of Marc Lenoir, Inserm U1051, France).</p>
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<p>Age-related hearing loss according to the International Organization for Standardization (ISO) 7029 standard. Shown are audiograms for females (<b>A</b>) and males (<b>B</b>). The <span class="html-italic">x</span>-axis displays the pure tone frequency (Hz) and the <span class="html-italic">y</span>-axis the hearing thresholds (dB HL). Each individual graph is representative of the median audiogram at a particular age (ranging from 20 to 70 years old, with increments of 10 years).</p>
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<p>Imbalance between anti-aging and pro-aging mechanisms with age. The scheme drawing numerates several anti-aging and pro-aging mechanisms identified in the cochlear aging process. Anti-aging mechanisms include estrogen, autophagic damage clearance, and mitochondrial dynamic. Pro-aging mechanisms include oxidative stress, DNA damage, mitochondrial dysfunction, senescence-like phenotype, and senescence-associated inflammation. During the aging process, decreased activity of anti-aging molecules and increased activity of pro-aging properties might lead to accumulation of mutations in mitochondrial DNA, increased lysosomal pH with a resulting accumulation of lipofuscin and aggregates, and nuclear DNA damage, leading to cochlear cell degeneration and age-related hearing loss.</p>
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<p>Functional and morphological assessments in SAMP8 and in SAMR1 mice. (<b>A</b>) Functional assessment. The compound action potential (CAP) threshold (red line) and distortion product otoacoustic emissions (DPOAE) amplitude (blue line) evoked by 20 kHz tone bursts, and endocochlear potential (EP) recordings (orange line, right axis)) in SAMR1 and SAMP8 mice. Fifty SAMP8 mice (n = 10 per age: 1, 3, 6, 12, 18 months) and 60 SAMR1 (n = 10 per age: 1, 3, 6, 12, 18, 24 months) mice were used for functional assessment. The lifespan of SAMR1 and SAMP8 was approximately 30 and 20 months, respectively. Note the earlier and faster increase in CAP threshold and decrease in DPOAE amplitude and EP value (arrowheads indicated broken-stick nonlinearities) in the SAMP8. In contrast to SAMR1, no CAP threshold nor DPOAEs could be recorded in 12-month-old SAMP8 mice, respectively. (<b>B</b>) Morphological assessment. Age-related loss of inner hair cells (IHCs, red line), outer hair cells (OHCs, blue line), and spiral ganglion neurons (SGNs, green line, right axis). At the end of the functional assessment period, the cochleae were removed and prepared for hair cell counting using SEM (n = 5 per age per strain) and SNG using light microscopy (n = 5 per age per strain). (<b>C</b>) Scanning electron microscopy in one and 12 months SAMP8 mice. Few OHCs are lacking (asterisks) among the three rows, but all IHCs are present at 1 month. The higher magnification insert shows an OHC stereociliary bundle with missing sterocilia (arrow). In a 12-month-old mouse, all OHCs and numerous IHCs (asterisks) have disappeared. The white box indicates a damaged IHC stereociliary bundle. In the insert, enlargement of the same IHC stereociliary bundle shows fused stereocilia. Scale bar = 10 µm; Insert in (<b>A</b>) = 1 µm. (<b>D</b>) Electron transmission microscopy of the stria vascularis. At one month, the three layers of strial cells, marginal (Mc), intermediate (Ic), basal (Bc) cells, and the blood vessels (Vx) appear normal. At 12 months, enlarged intercellular spaces and perivascular edema (asterisks) are seen. Scale bar = 10 µm. (<b>E</b>) Light microscopical evaluation of spiral ganglion loss. Shown is the normal aspect and density of neurons at 1 month, and a reduced number of spiral ganglion neurons at 12 months. Scale bar = 50 µm. (Adapted from Ménardo et al., [<a href="#B59-jcm-09-00218" class="html-bibr">59</a>]).</p>
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<p>Pharmacological mitigation of ROS prevents loss of hearing and hair cells in SAMP8 mice (<b>A</b>) SAMP8 mice and EUK-207. Shown are a SAMP8 mouse aged six months and the synthetic superoxide dismutase/catalase mimetic EUK-207. (<b>B</b>) Physiological assessment. The auditory brainstem response (ABR) thresholds recorded before (pale red plot) and after two months (pink plot) and three months (red plot) of Manitol treatments, or before (pale blue plot) and after two months (azure plot) and three months (blue plot) of EUK-207 (10 µM) treatments. (<b>C</b>) Morphological assessment. Representative scanning electron micrographs showing the basal regions of cochleae from Manitol-treated (left panel) and EUK-207-treated (right panel) SAMP8 mice after three months. Scale bar = 15 µm (Adapted from Benkafadar et al. [<a href="#B70-jcm-09-00218" class="html-bibr">70</a>]).</p>
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15 pages, 1142 KiB  
Opinion
Musical Training for Auditory Rehabilitation in Hearing Loss
by Jacques Pesnot Lerousseau, Céline Hidalgo and Daniele Schön
J. Clin. Med. 2020, 9(4), 1058; https://doi.org/10.3390/jcm9041058 - 8 Apr 2020
Cited by 11 | Viewed by 5374
Abstract
Despite the overall success of cochlear implantation, language outcomes remain suboptimal and subject to large inter-individual variability. Early auditory rehabilitation techniques have mostly focused on low-level sensory abilities. However, a new body of literature suggests that cognitive operations are critical for auditory perception [...] Read more.
Despite the overall success of cochlear implantation, language outcomes remain suboptimal and subject to large inter-individual variability. Early auditory rehabilitation techniques have mostly focused on low-level sensory abilities. However, a new body of literature suggests that cognitive operations are critical for auditory perception remediation. We argue in this paper that musical training is a particularly appealing candidate for such therapies, as it involves highly relevant cognitive abilities, such as temporal predictions, hierarchical processing, and auditory-motor interactions. We review recent studies demonstrating that music can enhance both language perception and production at multiple levels, from syllable processing to turn-taking in natural conversation. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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<p>Review of musical training protocols reported in scientific papers [<a href="#B7-jcm-09-01058" class="html-bibr">7</a>,<a href="#B24-jcm-09-01058" class="html-bibr">24</a>,<a href="#B25-jcm-09-01058" class="html-bibr">25</a>,<a href="#B26-jcm-09-01058" class="html-bibr">26</a>,<a href="#B27-jcm-09-01058" class="html-bibr">27</a>,<a href="#B28-jcm-09-01058" class="html-bibr">28</a>,<a href="#B29-jcm-09-01058" class="html-bibr">29</a>,<a href="#B30-jcm-09-01058" class="html-bibr">30</a>,<a href="#B31-jcm-09-01058" class="html-bibr">31</a>,<a href="#B32-jcm-09-01058" class="html-bibr">32</a>,<a href="#B33-jcm-09-01058" class="html-bibr">33</a>,<a href="#B34-jcm-09-01058" class="html-bibr">34</a>,<a href="#B35-jcm-09-01058" class="html-bibr">35</a>,<a href="#B36-jcm-09-01058" class="html-bibr">36</a>,<a href="#B37-jcm-09-01058" class="html-bibr">37</a>,<a href="#B38-jcm-09-01058" class="html-bibr">38</a>,<a href="#B39-jcm-09-01058" class="html-bibr">39</a>,<a href="#B40-jcm-09-01058" class="html-bibr">40</a>,<a href="#B41-jcm-09-01058" class="html-bibr">41</a>,<a href="#B42-jcm-09-01058" class="html-bibr">42</a>,<a href="#B43-jcm-09-01058" class="html-bibr">43</a>,<a href="#B44-jcm-09-01058" class="html-bibr">44</a>,<a href="#B45-jcm-09-01058" class="html-bibr">45</a>,<a href="#B46-jcm-09-01058" class="html-bibr">46</a>,<a href="#B47-jcm-09-01058" class="html-bibr">47</a>,<a href="#B48-jcm-09-01058" class="html-bibr">48</a>]. Each circle represents one study, plotted as a function of the average duration of the musical training and the average age of the participants. Color of the points indicates the content of the training, on a continuum from rhythmic only (drums only) to pitch only (songs, melodies) training. The size of the points indicates the sample size of the study (range: 6–163).</p>
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<p>Review of musical training effects for hearing impaired people [<a href="#B7-jcm-09-01058" class="html-bibr">7</a>,<a href="#B24-jcm-09-01058" class="html-bibr">24</a>,<a href="#B25-jcm-09-01058" class="html-bibr">25</a>,<a href="#B26-jcm-09-01058" class="html-bibr">26</a>,<a href="#B27-jcm-09-01058" class="html-bibr">27</a>,<a href="#B28-jcm-09-01058" class="html-bibr">28</a>,<a href="#B29-jcm-09-01058" class="html-bibr">29</a>,<a href="#B30-jcm-09-01058" class="html-bibr">30</a>,<a href="#B31-jcm-09-01058" class="html-bibr">31</a>,<a href="#B32-jcm-09-01058" class="html-bibr">32</a>,<a href="#B33-jcm-09-01058" class="html-bibr">33</a>,<a href="#B34-jcm-09-01058" class="html-bibr">34</a>,<a href="#B35-jcm-09-01058" class="html-bibr">35</a>,<a href="#B36-jcm-09-01058" class="html-bibr">36</a>,<a href="#B37-jcm-09-01058" class="html-bibr">37</a>,<a href="#B38-jcm-09-01058" class="html-bibr">38</a>,<a href="#B39-jcm-09-01058" class="html-bibr">39</a>,<a href="#B40-jcm-09-01058" class="html-bibr">40</a>,<a href="#B41-jcm-09-01058" class="html-bibr">41</a>,<a href="#B42-jcm-09-01058" class="html-bibr">42</a>,<a href="#B43-jcm-09-01058" class="html-bibr">43</a>,<a href="#B44-jcm-09-01058" class="html-bibr">44</a>,<a href="#B45-jcm-09-01058" class="html-bibr">45</a>,<a href="#B46-jcm-09-01058" class="html-bibr">46</a>,<a href="#B47-jcm-09-01058" class="html-bibr">47</a>,<a href="#B48-jcm-09-01058" class="html-bibr">48</a>]. Each circle represents one study, plotted as a function of the average age of the participants and the precisely measured effect. Black circles: statistically significant effects; white: non-significant. The size of the points indicates the sample size of the study (range: 6–163).</p>
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15 pages, 1407 KiB  
Perspective
Contemporary Speech and Oral Language Care for Deaf and Hard-of-Hearing Children Using Hearing Devices
by François Bergeron, Aurore Berland, Dominique Demers and Suzie Gobeil
J. Clin. Med. 2020, 9(2), 378; https://doi.org/10.3390/jcm9020378 - 30 Jan 2020
Cited by 9 | Viewed by 6118
Abstract
Contemporary speech and language interventions are not limited to disabilities but embrace the pragmatics of communication behaviors from the perspective of functional social participation. Accordingly, current speech and language therapies for deaf and hard-of-hearing children include a broad spectrum of approaches and techniques. [...] Read more.
Contemporary speech and language interventions are not limited to disabilities but embrace the pragmatics of communication behaviors from the perspective of functional social participation. Accordingly, current speech and language therapies for deaf and hard-of-hearing children include a broad spectrum of approaches and techniques. This paper explores contemporary approaches and techniques for speech and oral language interventions for deaf and hard-of-hearing children using hearing devices, evidence of efficacy and how they are implemented in diverse clinical practices. Full article
(This article belongs to the Special Issue Therapies for Hearing Loss)
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<p>(<b>a</b>). The International Classification of Functioning, Disability and Health (ICF) model [<a href="#B14-jcm-09-00378" class="html-bibr">14</a>]. (<b>b</b>). Human Development Model—Disability Creation Process (HDM-DCP) RIPPH 1998 [<a href="#B15-jcm-09-00378" class="html-bibr">15</a>].</p>
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<p>Relations between languages, approaches and techniques.</p>
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<p>Approach continuum.</p>
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<p>Continuum of Interprofessional Collaborative Practice in Health and Social Care [<a href="#B46-jcm-09-00378" class="html-bibr">46</a>]. + and − Complex indicators define the complexity of the needs of the person/close-ones/community and the biopsychosocial context in which these needs are to be met.</p>
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