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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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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