Electrophysiology and genetic testing in the precision medicine of congenital deafness: A review

Background: Congenital hearing loss is remarkably heterogeneous, with over 130 deafness genes and thousands of variants, making for innumerable genotype/phenotype combinations. Understanding both the pathophysiology of hearing loss and molecular site of lesion along the auditory pathway permits for...

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Main Authors: Kevin Y. Zhan, Oliver F. Adunka, Adrien Eshraghi, William J. Riggs, Sandra M. Prentiss, Denise Yan, Fred F. Telischi, Xuezhong Liu, Shuman He
Format: Article
Language:English
Published: Elsevier 2021-01-01
Series:Journal of Otology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1672293020300635
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spelling doaj-363bbb63585044e9963824ac42bdb64c2021-01-16T04:06:52ZengElsevierJournal of Otology1672-29302021-01-011614046Electrophysiology and genetic testing in the precision medicine of congenital deafness: A reviewKevin Y. Zhan0Oliver F. Adunka1Adrien Eshraghi2William J. Riggs3Sandra M. Prentiss4Denise Yan5Fred F. Telischi6Xuezhong Liu7Shuman He8Department of Otolaryngology – Head & Neck Surgery, The Ohio State University Wexner Medical Center, Columbus, OH, USADepartment of Otolaryngology – Head & Neck Surgery, The Ohio State University Wexner Medical Center, Columbus, OH, USA; Department of Audiology, Nationwide Children’s Hospital, Columbus, OH, USADepartment of Otolaryngology – Head & Neck Surgery, University of Miami Miller School of Medicine, Miami, FL, USADepartment of Otolaryngology – Head & Neck Surgery, The Ohio State University Wexner Medical Center, Columbus, OH, USA; Department of Audiology, Nationwide Children’s Hospital, Columbus, OH, USADepartment of Otolaryngology – Head & Neck Surgery, University of Miami Miller School of Medicine, Miami, FL, USADepartment of Otolaryngology – Head & Neck Surgery, University of Miami Miller School of Medicine, Miami, FL, USADepartment of Otolaryngology – Head & Neck Surgery, University of Miami Miller School of Medicine, Miami, FL, USADepartment of Otolaryngology – Head & Neck Surgery, University of Miami Miller School of Medicine, Miami, FL, USA; Dr. John T. MacDonald Foundation, Department of Human Genetics, University of Miami Miller School of Medicine, Miami, FL, USA; Corresponding author. Department of Otolaryngology – Head & Neck Surgery, Department of Human Genetics, John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL, USA.Department of Otolaryngology – Head & Neck Surgery, The Ohio State University Wexner Medical Center, Columbus, OH, USA; Department of Audiology, Nationwide Children’s Hospital, Columbus, OH, USA; Corresponding author. Department of Otolaryngology – Head and Neck Surgery, The Ohio State University, 915 Olentangy River Road, Suite 4000, Columbus, OH, 43212, USA.Background: Congenital hearing loss is remarkably heterogeneous, with over 130 deafness genes and thousands of variants, making for innumerable genotype/phenotype combinations. Understanding both the pathophysiology of hearing loss and molecular site of lesion along the auditory pathway permits for significantly individualized counseling. Electrophysiologic techniques such as electrocochleography (ECochG) and electrically-evoked compound action potentials (eCAP) are being studied to localize pathology and estimate residual cochlear vs. neural health. This review describes the expanding roles of genetic and electrophysiologic evaluation in the precision medicine of congenital hearing loss.The basics of genetic mutations in hearing loss and electrophysiologic testing (ECochG and eCAP) are reviewed, and how they complement each other in the diagnostics and prognostication of hearing outcomes. Used together, these measures improve the understanding of insults to the auditory system, allowing for individualized counseling for CI candidacy/outcomes or other habilitation strategies. Conclusion: Despite tremendous discovery in deafness genes, the effects of individual genes on neural function remain poorly understood. Bridging the understanding between molecular genotype and neural and functional phenotype is paramount to interpreting genetic results in clinical practice. The future hearing healthcare provider must consolidate an ever-increasing amount of genetic and phenotypic information in the precision medicine of hearing loss.http://www.sciencedirect.com/science/article/pii/S1672293020300635ElectrophysiologyGeneticsHearing lossECAPECocHG
collection DOAJ
language English
format Article
sources DOAJ
author Kevin Y. Zhan
Oliver F. Adunka
Adrien Eshraghi
William J. Riggs
Sandra M. Prentiss
Denise Yan
Fred F. Telischi
Xuezhong Liu
Shuman He
spellingShingle Kevin Y. Zhan
Oliver F. Adunka
Adrien Eshraghi
William J. Riggs
Sandra M. Prentiss
Denise Yan
Fred F. Telischi
Xuezhong Liu
Shuman He
Electrophysiology and genetic testing in the precision medicine of congenital deafness: A review
Journal of Otology
Electrophysiology
Genetics
Hearing loss
ECAP
ECocHG
author_facet Kevin Y. Zhan
Oliver F. Adunka
Adrien Eshraghi
William J. Riggs
Sandra M. Prentiss
Denise Yan
Fred F. Telischi
Xuezhong Liu
Shuman He
author_sort Kevin Y. Zhan
title Electrophysiology and genetic testing in the precision medicine of congenital deafness: A review
title_short Electrophysiology and genetic testing in the precision medicine of congenital deafness: A review
title_full Electrophysiology and genetic testing in the precision medicine of congenital deafness: A review
title_fullStr Electrophysiology and genetic testing in the precision medicine of congenital deafness: A review
title_full_unstemmed Electrophysiology and genetic testing in the precision medicine of congenital deafness: A review
title_sort electrophysiology and genetic testing in the precision medicine of congenital deafness: a review
publisher Elsevier
series Journal of Otology
issn 1672-2930
publishDate 2021-01-01
description Background: Congenital hearing loss is remarkably heterogeneous, with over 130 deafness genes and thousands of variants, making for innumerable genotype/phenotype combinations. Understanding both the pathophysiology of hearing loss and molecular site of lesion along the auditory pathway permits for significantly individualized counseling. Electrophysiologic techniques such as electrocochleography (ECochG) and electrically-evoked compound action potentials (eCAP) are being studied to localize pathology and estimate residual cochlear vs. neural health. This review describes the expanding roles of genetic and electrophysiologic evaluation in the precision medicine of congenital hearing loss.The basics of genetic mutations in hearing loss and electrophysiologic testing (ECochG and eCAP) are reviewed, and how they complement each other in the diagnostics and prognostication of hearing outcomes. Used together, these measures improve the understanding of insults to the auditory system, allowing for individualized counseling for CI candidacy/outcomes or other habilitation strategies. Conclusion: Despite tremendous discovery in deafness genes, the effects of individual genes on neural function remain poorly understood. Bridging the understanding between molecular genotype and neural and functional phenotype is paramount to interpreting genetic results in clinical practice. The future hearing healthcare provider must consolidate an ever-increasing amount of genetic and phenotypic information in the precision medicine of hearing loss.
topic Electrophysiology
Genetics
Hearing loss
ECAP
ECocHG
url http://www.sciencedirect.com/science/article/pii/S1672293020300635
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