- OVERALL The overarching goal of the proposed research is to advance our understanding of age-related hearing loss (presbyacusis). More than 37 million American adults have impaired hearing and this number is rising rapidly due to our growing aging society. Interventions for presbyacusis have relatively limited effectiveness, due in part to our incomplete understanding of the distinct metabolic, sensory, and neural mechanisms underlying hearing and communication difficulties in older adults. Four integrated scientific projects are supported by a human subjects core and will test hypotheses about the pathophysiology and genetic, molecular, and cellular mechanisms underlying presbyacusis, examine their consequences for communication, develop tools that improve the diagnostic specificity of presbyacusis, and provide guidance for individualized interventions. Project 1 identifies genetic variants for presbyacusis, characterizes their associated pathophysiology, defines their effects on hearing loss, and assesses the pathologic consequences of these variants in human temporal bones. Project 2 examines how age-dependent changes in the cochlea's innate immune system contribute to degeneration of the cochlear lateral wall and auditory nerve, leading to metabolic and neural presbyacusis. Project 3 uses unique physiologic metrics shared with Project 2 that differentiate metabolic, sensory, and neural presbyacusis in human subjects. Using these same subjects, Project 4 examines acoustic-level phonetic cue and executive system explanations for why older adults experience speech recognition difficulties. Thus, the four scientific projects are interrelated and complementary across levels of analysis to integrate data from animal models, human subjects, and human tissue for the extensive characterization of the pathophysiology of presbyacusis from the inner ear to cortex. Core A (Administration) provides and supports an administrative structure to integrate all scientific activities of the Clinical Research Center. Core B (Human Subjects) recruits human subjects and coordinates their schedules, and supports collection, storage, and analysis of data, which are shared with other research groups to confirm our findings and extend the impact of our research. Together, the proposed research and comprehensive longitudinal human subject database form a cohesive, translational program that will advance our understanding of human presbyacusis and promote scientific progress through sharing of data and presbyacusis phenotyping tools. The Clinical Research Center is unique because of its 30-year longitudinal study of hearing in older adults, clinical and translational approaches, and a focus on providing strong evidence to enhance hearing health care for the millions of Americans who have reduced quality of life because of poorer hearing and communication abilities. The Center will continue to guide the theoretical and clinical study of audition and precision treatments for presbyacusis.

Public Health Relevance

? OVERALL The Clinical Research Center leverages the multidisciplinary and wide-ranging expertise in each scientific project, and the wealth of information available in the human subject database, to generate new knowledge about the high-prevalence public health concern of age-related hearing loss (presbyacusis). Our long-term goals are to reduce its prevalence, slow its progression, and develop new prevention, diagnostic, and treatment strategies to improve communication and the quality of life of millions of older adults.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Specialized Center (P50)
Project #
3P50DC000422-31A1S1
Application #
10191146
Study Section
Special Emphasis Panel (ZDC1)
Program Officer
King, Kelly Anne
Project Start
1997-07-01
Project End
2024-08-31
Budget Start
2019-09-13
Budget End
2020-08-31
Support Year
31
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Medical University of South Carolina
Department
Otolaryngology
Type
Schools of Medicine
DUNS #
183710748
City
Charleston
State
SC
Country
United States
Zip Code
29407
Noble, Kenyaria V; Reyzer, Michelle L; Barth, Jeremy L et al. (2018) Use of Proteomic Imaging Coupled With Transcriptomic Analysis to Identify Biomolecules Responsive to Cochlear Injury. Front Mol Neurosci 11:243
Simpson, Annie N; Simpson, Kit N; Dubno, Judy R (2018) Healthcare Costs for Insured Older U.S. Adults with Hearing Loss. J Am Geriatr Soc 66:1546-1552
Lewis, Morag A; Nolan, Lisa S; Cadge, Barbara A et al. (2018) Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes. BMC Med Genomics 11:77
Bologna, William J; Vaden Jr, Kenneth I; Ahlstrom, Jayne B et al. (2018) Age effects on perceptual organization of speech: Contributions of glimpsing, phonemic restoration, and speech segregation. J Acoust Soc Am 144:267
Panganiban, Clarisse H; Barth, Jeremy L; Darbelli, Lama et al. (2018) Noise-induced dysregulation of Quaking RNA binding proteins contributes to auditory nerve demyelination and hearing loss. J Neurosci :
Chiarello, Christine; Vaden Jr, Kenneth I; Eckert, Mark A (2018) Orthographic influence on spoken word identification: Behavioral and fMRI evidence. Neuropsychologia 111:103-111
Harris, Kelly C; Vaden Jr, Kenneth I; McClaskey, Carolyn M et al. (2018) Complementary metrics of human auditory nerve function derived from compound action potentials. J Neurophysiol 119:1019-1028
McRackan, Theodore R; Fabie, Joshua E; Burton, Jane A et al. (2018) Earphone and Aided Word Recognition Differences in Cochlear Implant Candidates. Otol Neurotol 39:e543-e549
Dubno, Judy R (2018) Beyond the audiogram: application of models of auditory fitness for duty to assess communication in the real world. Int J Audiol 57:321-322
McRackan, Theodore R; Clinkscales, William B; Ahlstrom, Jayne B et al. (2018) Factors associated with benefit of active middle ear implants compared to conventional hearing aids. Laryngoscope 128:2133-2138

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