Researcher using optical coherance tomography (OCT) to see inside patient's ear for diagnosis. Photo Credit: Chris Shinn.

Otology, Neurotology, and Skull Base Surgery

The Division of Otology, Neurotology, and Skull Base Surgery stands at the forefront of pioneering research aimed at restoring hearing and preventing hearing loss in both adult and pediatric patients.

  • Of babies born in the United States, 2 to 3 of every 1,000 have a detectable hearing loss in at least one ear and 1 out of 500 newborns suffers from significant hearing impairment. Congenital hearing loss (hearing loss present at birth) can include hereditary hearing loss or hearing loss due to other factors present either in the womb during pregnancy or at the time of birth.

    When a child is born, their inner ear or cochlea is sensitive to sound but may require some postnatal refinement. Also, the brain has to learn how to perceive sound and speech from the information coming up the auditory pathway. Children can be born with pathology to the outer or middle ear, sensory hair cells, hearing organ (Organ of Corti within the cochlea), or they can be born without auditory nerves which carry the hearing information to the brain. Without intervention, hearing loss can affect a child’s ability to develop speech, language, and social skills as well as achieve academic success. The earlier children with hearing loss receive intervention, the more likely they are to reach their full potential. Otologists and audiologists work together to recommend and implement hearing aids, cochlear implants, auditory brain stem implants, and various types of rehabilitative therapy.

    Recently, a team of multidisciplinary researchers led a breakthrough (NIH)-funded clinical trial that attempts to show that young children born without a hearing nerve can safely undergo an auditory brainstem implant (ABI) surgery. The study also allowed our researchers to study how the brain develops over time and how it learns to hear sound and develop speech. A separate NIH-funded study examines the effects of cochlear implantation on language, behavioral, and societal outcomes in children. Other efforts are using otoacoustic emissions (echoes and distortion tones from the ear) to understand how the newborn cochlea functions and to develop new and advanced diagnostic tests.

    Faculty Researchers:
    Carolina Abdala, PhD
    John Oghalai, MD
    Joni K. Doherty, MD, PhD
    David R. Friedland, MD, PhD
    Raymond Goldsworthy, PhD
    Laurie Eisenberg, PhD
    Janet Choi, MD, MPH
    Raymond Kung, MD
    Seiji B. Shibata, MD, PhD

  • Hearing loss is the third most common health problem in the United States and affects all ages including newborn babies to elderly adults. About 48 million Americans (1 out of 8 people) have lost some hearing. Of babies born in the U.S., 2 to 3 of every 1,000 have a detectable hearing loss in at least one ear and 1 out of 500 newborns suffers from significant hearing impairment. 1 out of 3 adults aged 65-74 have disabling hearing loss, and that number increases to 1 out of 2 adults over the age of 75.

    Causes of hearing loss can include aging, ototoxic drugs, noise exposure, head trauma, infection, and genetic conditions and predispositions. Once mechanosensory hair cells in the human inner ear are damaged and lost by any of a variety of reasons, they never regenerate. Hence, a majority of sensorineural hearing loss is permanent and significantly affects the patient’s quality of life. Research indicates that people with hearing loss can have higher rates of depression, social isolation and cognitive decline.

    Researchers and clinicians in the Caruso Department are leading a unique interdisciplinary effort which uses the latest technology in hearing science, genetics, stem cell medicine, neuroscience, neuroimaging, and biomedical engineering to conduct hearing and otological research. Our Aim is to diagnose and restore hearing through a variety of methods including hearing aids, cochlear implantation, auditory brain stem implants, bone conductive hearing devices, and to explore the future of restoring hair cell function through regeneration therapies. Building on recent stem cell research, our department is working on the possibility of regenerating hair cells in humans. By determining the mechanisms of cell regulation, scientists hope to develop a biological, curative approach that will trigger natural replacement of those hair cells in order to initiate significant improvements in hearing.

    Faculty Researchers:
    Carolina Abdala, PhD
    Christopher Shera, PhD
    John Oghalai, MD
    Joni K. Doherty, MD, PhD
    David R. Friedland, MD, PhD
    Karolina Charaziak, PhD
    Janet Choi, MD, MPH
    Raymond Kung, MD
    Seiji B. Shibata, MD, PhD
    John Parsons, AuD

Labs

We have several major labs working on efforts to cure hearing loss.

John S. Oghalai, MD

The Oghalai Lab

The Oghalai lab at the Zilkha Neurogenetics Institute seeks to better understand the fundamental changes in cochlear function that underlie progressive hearing loss and to develop novel techniques to treat this problem before it leads to deafness. Clinically, our ultimate goal is to improve human health not only by caring for our patients expertly, but also by advancing our scientific knowledge base so that all physicians can treat disease more effectively.

Carolina Abdala, PhD

The Abdala Lab

The Abdala Lab, within the USC Caruso Department of Otolaryngology, studies natural changes in cochlear mechanics throughout the arc of the human lifespan. This research aims to provide a normative framework, but also to explore the mechanisms driving such change. Recent work is focused on the potential development and application of a combined reflection (SFOAE) and distortion (DPOAE) OAE protocol to understand and describe underlying deficits, not just detect and label sensorineural hearing loss.

Christopher Shera, PhD

The Auditory Physics Group

The Auditory Physics Group in the Caruso Department of Otolaryngology works to solve fundamental problems in the mechanics and physiology of the auditory system. Current interests of the group include comparative cochlear mechanics, cochlear nonlinearity and amplification, middle-ear mechanics, and otoacoustic emissions.

Brian Applegate, PhD

The Applegate Lab

Our research interests are broadly to develop novel biophotonic technologies for point-of-care diagnosis and monitoring of human disease as well as the basic scientific understanding of human disease. Our primary application area is functional imaging of the middle and inner ear. We are working toward advanced diagnostics for patient care as well as advanced imaging systems for probing the fundamental mechanics of the ear.

Radha Kalluri, PhD

The Kalluri Lab

The Kalluri Lab at the Zilkha Neurogentic Institute, led by Radha Kalluri, PhD, assistant professor of otolaryngology, explores the cochlea, an elegant hydromechanical structure in the ear, that which works to separate sounds of different frequencies and maps them onto a different place on the sensory epithelium. Specialized sensory cells that provide feedback forces to actively amplify local mechanical resonances refine this frequency-place map within the cochlea. Research is focused on understanding the biophysical mechanisms by which the auditory periphery parses frequency and intensity information, and how these functions degrade with hearing loss.

Raymond Goldsworthy, PhD

The Goldsworthy Lab

The Bionic Ear Lab in the Caruso Department of Otolaryngology explores ways of improving hearing for cochlear implant recipients. A focus of the lab is to optimize stimulation timing to provide better musical pitch and refined spatial hearing for cochlear implant users. Our lab emphasizes the importance of auditory training and neural plasticity in achieving optimal outcomes.

Karolina Charaziak, PhD

The Charaziak Lab

Research at the Charaziak lab is focused on understanding how the cochlea of the inner ear processes sounds. We utilize approaches that combine both direct (e.g., intracochlear vibrometry) and indirect (e.g., otoacoustic emissions) measurements of cochlear responses in animals with theoretical modeling. Joint intracochlear and otoacoustic emission (OAE) studies informed by theoretical models are crucial for improving the power of OAE-based diagnostics in humans, where the cochlea cannot be accessed for a direct study.

James Dewey, PhD

The Dewey Lab

The Dewey Lab at the Zilkha Neurogenetic Institute examines how structures within the inner ear vibrate in response to sound, how these vibrations are amplified by sensory hair cells, and how this amplification process leads to emission of sound from the ear. The overarching aims of this research are to understand the mechanisms underlying sensitive, normal hearing, and to improve how we detect and diagnose common forms of hearing loss.

Ksenia Gnedeva, PhD

The Gnedeva Lab

In the Gnedeva Lab at the Zilkha Neurogenetic Institute, we investigate how the mechanical microenvironment controls sensory organ development and directs tissue repair after damage. Although the focus of our research is on hearing and balance restoration, we are interested in the common mechanisms that suppress regeneration in the specialized sensory tissues.

Janet Choi, MD, MPH

The Choi Lab

The Choi Lab explores the impact of hearing loss treatment on healthy aging, with an emphasis on improving the accessibility and affordability of hearing healthcare. The team leverages both epidemiological data and clinical trials to investigate how hearing loss and the use of hearing devices affect social engagement and cognitive function. They also develop technology-based strategies to make medical and surgical hearing care options more comprehensible and accessible for individuals with hearing loss.

(Normal (wild type) mouse auditory nerve is demonstrated; the neuron specific TUJ1 (green) staining overlaps with the Tdtomato (red) positive afferent neurons. The deafened (Td/PVcre) mouse lacks Tdtomato afferent neurons but few TUJ1positive neurons which are consistent efferent neurons. This indicates selective afferent nerve denervation in our mouse model. This mouse model will serve as a valuable platform to test auditory nerve regeneration.. Photo Credit: Shibata Lab)
Seiji B. Shibata, MD, PhD

The Shibata Lab

In the Shibata lab at the Zilkha Neurogenetics Institute, our lab focuses on developing interventions to maintain, repair, and regenerate neurons in the inner ear. We seek to better understand the biology associated with sensorineural hearing loss resulting from cochlear nerve damage. Our goal is to regenerate functional afferent cochlear neurons from surviving inner ear non-sensory cells via direct reprogramming utilizing gene therapy.