The overall purpose of this proposal is to explore relationships between the reception of spoken language and the functional neuroanatomy of brain responses to speech listening by combining traditional measures of speech perception with state-of-the-art brain imaging with Single Photon Emission Computed Tomography (SPECT). Studies included in this proposal aim to identify cortical regions that subserve or participate in the reception of spoken language. The biological bases of spoken language reception will be explored by investigating regional cerebral blood flow (rCBF) in individuals with normal hearing and individuals who experience difficulty with the reception of spoken language because of varying degrees of hearing impairments. Several key questions will be addressed including: 1) what brain regions are activated in individuals with normal hearing and language reception versus individuals who experience difficulty with language reception because of hearing impairments, and 2) how do abnormalities in cortical activation responses related to clinical measures of audiometric performance , auditory evoked potentials, speech perception performance, communication difficulty indices, and lipreading capability, as well as to demographic variables such as age of hearing loss onset, etiology, and type of hearing loss intervention.
The specific aims are to: 1) document cerebral neural circuitry activated during spoken language reception in individuals with normal hearing in response to normal or acoustically manipulated signals, 2) determine if rCBF responses to speech stimuli are blunted in magnitude and/or altered in neuroanatomic distribution in individuals with varying degrees of hearing impairments, 3) examine if abnormal rCBF responses occur even when auditory evoked responses are intact, 4) characterize relationships between clinical measures of speech perception and rCBF responses, and 5) explore how demographic variables relate to rCBF changes. RCBF will be measured under three tasks: Full audio (presented either binaurally or monoaurally), degraded audio (incorporating manipulations to the spectral and temporal and content of the signals), and visual only presentations. Data from these studies will address several key areas in the NIDCD Strategic Plan including the development and application of """"""""novel techniques, e.g., functional imaging to assess structural and functional plasticity"""""""" and the NIH Consensus Development Conferences on Cochlear Implants in Adults and Children which called for """"""""new tools, such as functional brain imaging, to be applied to unexplored variables such as the ability of the implant to activate the central auditory system.""""""""

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
1R01DC004558-01
Application #
6176862
Study Section
Special Emphasis Panel (ZRG1-BBBP-3 (01))
Program Officer
Donahue, Amy
Project Start
2000-09-27
Project End
2003-08-31
Budget Start
2000-09-27
Budget End
2001-08-31
Support Year
1
Fiscal Year
2000
Total Cost
$458,922
Indirect Cost
Name
University of Texas-Dallas
Department
Psychology
Type
Other Domestic Higher Education
DUNS #
City
Richardson
State
TX
Country
United States
Zip Code
75080
Tobey, Emily A; Britt, Lana; Geers, Ann et al. (2012) Cochlear implantation updates: the Dallas Cochlear Implant Program. J Am Acad Audiol 23:438-45
Tobey, Emily A (2012) Current clinical research involving cochlear implantation. J Am Acad Audiol 23:384
Devous Sr, Michael D; Altuna, Dianne; Furl, Nicholas et al. (2006) Maturation of speech and language functional neuroanatomy in pediatric normal controls. J Speech Lang Hear Res 49:856-66
Tobey, Emily A; Devous Sr, Michael D; Buckley, Kristi et al. (2005) Pharmacological enhancement of aural habilitation in adult cochlear implant users. Ear Hear 26:45S-56S
Tobey, Emily A; Devous Sr, Michael D; Buckley, Kristi et al. (2004) Functional brain imaging as an objective measure of speech perception performance in adult cochlear implant users. Int J Audiol 43 Suppl 1:S52-6