Summary: Researchers report many hearing tests fail to pick up a common form of inner ear damage that leads to hearing loss.
Source: University at Buffalo.
Traditional clinical hearing tests often fail to diagnose patients with a common form of inner ear damage that might otherwise be detected by more challenging behavioral tests, according to the findings of a University at Buffalo-led study published in the journal Frontiers in Neuroscience.
This type of “hidden hearing loss” paradoxically presents itself as essentially normal hearing in the clinic, where audiograms — the gold-standard for measuring hearing thresholds — are typically conducted in a quiet room.
The reason some forms of hearing loss may go unrecognized in the clinic is that hearing involves a complex partnership between the ear and the brain. It turns out that the central auditory system can compensate for significant damage to the inner ear by turning up its volume control, partially overcoming the deficiency, explains Richard Salvi, SUNY Distinguished Professor of Communicative Disorders and Sciences and director of UB’s Center for Hearing and Deafness, and the study’s lead author.
“You can have tremendous damage to inner hair cells in the ear that transmit information to the brain and still have a normal audiogram,” says Salvi. “But people with this type of damage have difficulty hearing in certain situations, like hearing speech in a noisy room. Their thresholds appear normal. So they’re sent home.”
To understand why a hearing test isn’t identifying a hearing problem it’s necessary to follow the auditory pathway as sound-evoked neural signals travel from the ear to the brain.
About 95 percent of sound input to the brain comes from the ear’s inner hair cells.
“These inner hair cells are like spark plugs in an 8-cylinder engine,” says Salvi. “A car won’t run well if you remove half of those spark plugs, but people can still present with normal hearing thresholds if they’ve lost half or even three-quarters of their inner hair cells.”
Ear damage reduces the signal that goes the brain. That results in trouble hearing, but that’s not what’s happening here, because the brain “has a central gain control, like a radio, the listener can turn up the volume control to better hear a distant station.” Salvi says.
Sound is converted to neural activity by the inner hair cells in the auditory part of the ear, called the cochlea.
Sound-evoked neural activity then travels from the cochlea to the auditory nerve and into the central auditory pathway of the brain. Halfway up the auditory pathway the information is relayed into a structure known as the inferior colliculus, before finally arriving at the auditory cortex in the brain, where interpretation of things like speech take place.
For people with inner hair cell loss, sound is less faithfully converted to neural activity in the cochlea. However, this weakened sound-evoked activity is progressively amplified as it travels along the central auditory pathway to the inferior colliculus and onward. By the time it reaches the auditory cortex, things are hyperactive because the brain has recognized a problem.
“Once the signal gets high enough to activate a few neurons it’s like your brain has a hearing aid that turns up the volume,” says Salvi.
It’s not clear how many people might have this type of hearing loss, but Salvi says it is a common complaint to have difficulty hearing in noisy environments as people get older. The perceptual consequences include apparently normal hearing for tests administered in quiet settings, but adding background noise often results in deficits in detecting and recognizing sounds.
“That’s why the way we’re measuring hearing in the clinic may not be adequate for subtle forms of hearing loss,” says one of the study’s co-authors, Benjamin Auerbach, a postdoctoral fellow at UB’s Center for Hearing and Deafness.
In addition to informing how hearing tests are conducted, Auerbach suggests that this compensation might be causing or contributing to other auditory perceptual disorders such as tinnitus, often described as a ringing in the ears, or hyperacusis, a condition that causes moderate everyday sounds to be perceived as intolerably loud.
“If you have excessive gain in the central auditory system, it could result in the over-amplification of sound or even make silence sound like noise,” says Auerbach.
Source: Bert Gambini – University at Buffalo
Image Source: NeuroscienceNews.com image is adapted from the University at Buffalo news release.
Original Research: Full open access research for “Inner Hair Cell Loss Disrupts Hearing and Cochlear Function Leading to Sensory Deprivation and Enhanced Central Auditory Gain” by Richard Salvi, Wei Sun, Dalian Ding, Guang-Di Chen, Edward Lobarinas, Jian Wang, Kelly Radziwon and Benjamin D. Auerbach in Frontiers in Neuroscience. Published online January 18 2017 doi:10.3389/fnins.2016.00621
[cbtabs][cbtab title=”MLA”]University at Buffalo “Hearing Tests Miss Common Form of Hearing Loss.” NeuroscienceNews. NeuroscienceNews, 18 April 2017.
<https://neurosciencenews.com/hearing-tests-deafness-6435/>.[/cbtab][cbtab title=”APA”]University at Buffalo (2017, April 18). Hearing Tests Miss Common Form of Hearing Loss. NeuroscienceNew. Retrieved April 18, 2017 from https://neurosciencenews.com/hearing-tests-deafness-6435/[/cbtab][cbtab title=”Chicago”]University at Buffalo “Hearing Tests Miss Common Form of Hearing Loss.” https://neurosciencenews.com/hearing-tests-deafness-6435/ (accessed April 18, 2017).[/cbtab][/cbtabs]
Abstract
Inner Hair Cell Loss Disrupts Hearing and Cochlear Function Leading to Sensory Deprivation and Enhanced Central Auditory Gain
There are three times as many outer hair cells (OHC) as inner hair cells (IHC), yet IHC transmit virtually all acoustic information to the brain as they synapse with 90–95% of type I auditory nerve fibers. Here we review a comprehensive series of experiments aimed at determining how loss of the IHC/type I system affects hearing by selectively destroying these cells in chinchillas using the ototoxic anti-cancer agent carboplatin. Eliminating IHC/type I neurons has no effect on distortion product otoacoustic emission or the cochlear microphonic potential generated by OHC; however, it greatly reduces the summating potential produced by IHC and the compound action potential (CAP) generated by type I neurons. Remarkably, responses from remaining auditory nerve fibers maintain sharp tuning and low thresholds despite innervating regions of the cochlea with ~80% IHC loss. Moreover, chinchillas with large IHC lesions have surprisingly normal thresholds in quiet until IHC losses exceeded 80%, suggesting that only a few IHC are needed to detect sounds in quiet. However, behavioral thresholds in broadband noise are elevated significantly and tone-in-narrow band noise masking patterns exhibit greater remote masking. These results suggest the auditory system is able to compensate for considerable loss of IHC/type I neurons in quiet but not in difficult listening conditions. How does the auditory brain deal with the drastic loss of cochlear input? Recordings from the inferior colliculus found a relatively small decline in sound-evoked activity despite a large decrease in CAP amplitude after IHC lesion. Paradoxically, sound-evoked responses are generally larger than normal in the auditory cortex, indicative of increased central gain. This gain enhancement in the auditory cortex is associated with decreased GABA-mediated inhibition. These results suggest that when the neural output of the cochlea is reduced, the central auditory system compensates by turning up its gain so that weak signals once again become comfortably loud. While this gain enhancement is able to restore normal hearing under quiet conditions, it may not adequately compensate for peripheral dysfunction in more complex sound environments. In addition, excessive gain increases may convert recruitment into the debilitating condition known as hyperacusis.
“Inner Hair Cell Loss Disrupts Hearing and Cochlear Function Leading to Sensory Deprivation and Enhanced Central Auditory Gain” by Richard Salvi, Wei Sun, Dalian Ding, Guang-Di Chen, Edward Lobarinas, Jian Wang, Kelly Radziwon and Benjamin D. Auerbach in Frontiers in Neuroscience. Published online January 18 2017 doi:10.3389/fnins.2016.00621
