Carolina Abdala, PhD

Professor of Otolaryngology-Head and Neck Surgery

Co-Division Chief

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Overview

Human Cochlear Function: A Continuum of Maturation and Aging.
This project studies changes in cochlear function throughout the human lifespan, defining the timeline for these age-related shifts and the mechanisms driving the changes. We use primarily otoacaoustic emissions, a noninvasive ear canal probe of cochlear mechanics to learn about the human peripheral system. We apply both distortion- (DPOAE) and reflection-source (stimulus frequency OAEs and the reflection-component of the DPOAE) emissions using custom-algorithms, innovative swept-tone methodology and advanced analysis schemes. We disentangle the origin of age-related effects by separating distortion product OAEs into their dual components, distortion and reflection; and studying how each component’s phase and amplitude is impacted throughout the human lifespan. In our lab it is important to study both apical and basal halves of the cochlea to yield a more comprehensive understanding of how the cochlea codes low and high-frequency sounds. The apex has been minimally studied in humans, and wholly unexplored during maturation. Yet, we have recently reported striking immaturities in DPOAE phase for low-frequency signals coded in the apex of neonates. Our exploration of human cochlear function from base to apex using multiple OAE sources establishes a normative framework, provides detailed information about newborn cochlear maturation, and probes how the elderly cochlea ages into senescence. These findings contribute to more comprehensive cochlear models and toward the development of more innovative probes of cochlear function for human application. This project is funded by the NIH-NIDCD.

Exploiting Dual OAE Sources to Study the Normal and Impaired Human Cochlea.
This project attempts to exploit the distinct information embedded in reflection- and distortion-source OAEs to create a more comprehensive and descriptive joint test of cochlear function. At present, OAEs are used in a categorical sense, simply to detect hearing loss. However, once hearing loss is detected, we wish to learn about the underlying deficit and etiology. The ample information provided by the two OAE types (i.e. linear reflection and nonlinear distortion) can offer distinct clues about different aspects of cochlear function. We wish to exploit this distinct information to describe (not just detect) sensorineural hearing loss (SNHL). At present, SNHL is a catch-all term, defined by degree of loss and audiometric configuration. However, two hearing losses with identical audiograms can produce varying perceptual difficulties and varied success with hearing aids. By recording a combined reflection and distortion OAE profile over broad level and frequency ranges, we may be able to learn more about the underlying deficits that comprise the broad and vague category of SNHL. When used in combination, the properties embodied by each OAE can be considered in one joint metric. We are currently developing and testing this joint OAE protocol by recording stimulus frequency OAEs and the distortion component of DPOAEs in ears with normal and impaired hearing. This project is conducted in collaboration with fellow USC faculty member Dr. Christopher Shera.

https://sites.usc.edu/abdalab/

Research Funding

  • Advanced Detection and Differential Diagnosis of Hearing Loss Using Otoacoustic Emissions
    NIH · R01DC018307 · Sep 1, 2020 – Aug 31, 2026 · Role: Principal Investigator
  • Otoacoustic Emissions: Evoking the Future
    NIH · R13DC016825 · Sep 19, 2017 – Aug 31, 2018 · Role: Co-Principal Investigator
  • Human Cochlear Function: A Continuum of Maturation and Aging
    NIH · R01DC003552 · Aug 1, 1998 – Jul 31, 2021 · Role: Principal Investigator
  • DEVELOPMENT OF HUMAN COCHLEAR FUNCTION
    NIH · R29DC003552 · Aug 1, 1998 – Jul 31, 2003 · Role: Principal Investigator

Publications

  • Changes in the DP-gram during the preterm and early postnatal period. Ear Hear. 2008 Aug; 29(4):512-23.. View in PubMed
  • A comparative study of distortion-product-otoacoustic-emission fine structure in human newborns and adults with normal hearing. J Acoust Soc Am. 2007 Oct; 122(4):2191-202.. View in PubMed
  • Distortion product otoacoustic emission suppression tuning and acoustic admittance in human infants: birth through 6 months. J Acoust Soc Am. 2007 Jun; 121(6):3617-27.. View in PubMed
  • Theory of forward and reverse middle-ear transmission applied to otoacoustic emissions in infant and adult ears. J Acoust Soc Am. 2007 Feb; 121(2):978-93.. View in PubMed
  • Effects of middle-ear immaturity on distortion product otoacoustic emission suppression tuning in infant ears. J Acoust Soc Am. 2006 Dec; 120(6):3832-42.. View in PubMed
  • Effects of aspirin on distortion product otoacoustic emission suppression in human adults: a comparison with neonatal data. J Acoust Soc Am. 2005 Sep; 118(3 Pt 1):1566-75.. View in PubMed
  • Distortion product otoacoustic emission (2f1-f2) suppression in 3-month-old infants: evidence for postnatal maturation of human cochlear function? J Acoust Soc Am. 2004 Dec; 116(6):3572-80. Abdala C . View in PubMed
  • A longitudinal study of distortion product otoacoustic emission ipsilateral suppression and input/output characteristics in human neonates. J Acoust Soc Am. 2003 Dec; 114(6 Pt 1):3239-50.. View in PubMed
  • Ipsilateral distortion product otoacoustic emission (2f1-f2) suppression in children with sensorineural hearing loss. J Acoust Soc Am. 2003 Aug; 114(2):919-31.. View in PubMed
  • Progressive hearing loss in mice lacking the cyclin-dependent kinase inhibitor Ink4d. Nat Cell Biol. 2003 May; 5(5):422-6.. View in PubMed