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Human Cochlear Histopathology Reflects Clinical Signatures of Primary Neural Degeneration
Auditory neuropathy is a significant and understudied cause of human hearing loss, diagnosed in patients who demonstrate abnormal function of the cochlear nerve despite typical function of sensory cells. Because the human inner ear cannot be visualized during life, histopathological analysis of auto...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501826/ https://www.ncbi.nlm.nih.gov/pubmed/28687782 http://dx.doi.org/10.1038/s41598-017-04899-9 |
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author | Sagers, Jessica E. Landegger, Lukas D. Worthington, Steven Nadol, Joseph B. Stankovic, Konstantina M. |
author_facet | Sagers, Jessica E. Landegger, Lukas D. Worthington, Steven Nadol, Joseph B. Stankovic, Konstantina M. |
author_sort | Sagers, Jessica E. |
collection | PubMed |
description | Auditory neuropathy is a significant and understudied cause of human hearing loss, diagnosed in patients who demonstrate abnormal function of the cochlear nerve despite typical function of sensory cells. Because the human inner ear cannot be visualized during life, histopathological analysis of autopsy specimens is critical to understanding the cellular mechanisms underlying this pathology. Here we present statistical models of severe primary neuronal degeneration and its relationship to pure tone audiometric thresholds and word recognition scores in comparison to age-matched control patients, spanning every decade of life. Analysis of 30 ears from 23 patients shows that severe neuronal loss correlates with elevated audiometric thresholds and poor word recognition. For each ten percent increase in total neuronal loss, average thresholds across patients at each audiometric test frequency increase by 6.0 dB hearing level (HL). As neuronal loss increases, threshold elevation proceeds more rapidly in low audiometric test frequencies than in high frequencies. Pure tone average closely agrees with word recognition scores in the case of severe neural pathology. Histopathologic study of the human inner ear continues to emphasize the need for non- or minimally invasive clinical tools capable of establishing cellular-level diagnoses. |
format | Online Article Text |
id | pubmed-5501826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55018262017-07-10 Human Cochlear Histopathology Reflects Clinical Signatures of Primary Neural Degeneration Sagers, Jessica E. Landegger, Lukas D. Worthington, Steven Nadol, Joseph B. Stankovic, Konstantina M. Sci Rep Article Auditory neuropathy is a significant and understudied cause of human hearing loss, diagnosed in patients who demonstrate abnormal function of the cochlear nerve despite typical function of sensory cells. Because the human inner ear cannot be visualized during life, histopathological analysis of autopsy specimens is critical to understanding the cellular mechanisms underlying this pathology. Here we present statistical models of severe primary neuronal degeneration and its relationship to pure tone audiometric thresholds and word recognition scores in comparison to age-matched control patients, spanning every decade of life. Analysis of 30 ears from 23 patients shows that severe neuronal loss correlates with elevated audiometric thresholds and poor word recognition. For each ten percent increase in total neuronal loss, average thresholds across patients at each audiometric test frequency increase by 6.0 dB hearing level (HL). As neuronal loss increases, threshold elevation proceeds more rapidly in low audiometric test frequencies than in high frequencies. Pure tone average closely agrees with word recognition scores in the case of severe neural pathology. Histopathologic study of the human inner ear continues to emphasize the need for non- or minimally invasive clinical tools capable of establishing cellular-level diagnoses. Nature Publishing Group UK 2017-07-07 /pmc/articles/PMC5501826/ /pubmed/28687782 http://dx.doi.org/10.1038/s41598-017-04899-9 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sagers, Jessica E. Landegger, Lukas D. Worthington, Steven Nadol, Joseph B. Stankovic, Konstantina M. Human Cochlear Histopathology Reflects Clinical Signatures of Primary Neural Degeneration |
title | Human Cochlear Histopathology Reflects Clinical Signatures of Primary Neural Degeneration |
title_full | Human Cochlear Histopathology Reflects Clinical Signatures of Primary Neural Degeneration |
title_fullStr | Human Cochlear Histopathology Reflects Clinical Signatures of Primary Neural Degeneration |
title_full_unstemmed | Human Cochlear Histopathology Reflects Clinical Signatures of Primary Neural Degeneration |
title_short | Human Cochlear Histopathology Reflects Clinical Signatures of Primary Neural Degeneration |
title_sort | human cochlear histopathology reflects clinical signatures of primary neural degeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501826/ https://www.ncbi.nlm.nih.gov/pubmed/28687782 http://dx.doi.org/10.1038/s41598-017-04899-9 |
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