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Presbycusis (also spelled presbyacusis, from Greek πρέσβυς presbys "old" + ἄκουσις akousis "hearing"[1]), or age-related hearing loss, is the cumulative effect of aging on hearing. It is a progressive and irreversible bilateral symmetrical age-related sensorineural hearing loss resulting from degeneration of the cochlea or associated structures of the inner ear or auditory nerves. The hearing loss is most marked at higher frequencies. Hearing loss that accumulates with age but is caused by factors other than normal aging (nosocusis and sociocusis) is not presbycusis, although differentiating the individual effects of distinct causes of hearing loss can be difficult.

Presbycusis
SpecialtyOtorhinolaryngology, speech–language pathology, geriatrics Edit this on Wikidata

The cause of presbycusis is a combination of genetics, cumulative environmental exposures and pathophysiological changes related to aging.[2] At present there are no preventive measures known; treatment is by hearing aid or surgical implant.

Presbycusis is the most common cause of hearing loss, affecting one out of three persons by age 65, and one out of two by age 75. Presbycusis is the second most common illness next to arthritis in aged people.

Many vertebrates such as fish, birds and amphibians do not experience presbycusis in old age as they are able to regenerate their cochlear sensory cells, whereas mammals including humans have genetically lost this regenerative ability.

Presentation

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Primary symptoms:

Secondary symptoms:

  • hyperacusis, heightened sensitivity to certain volumes and frequencies of sound, resulting from "recruitment"
  • tinnitus, ringing, buzzing, hissing or other sounds in the ear when no external sound is present

Usually occurs after age 50, but deterioration in hearing has been found to start very early, from about the age of 18 years. The ISO standard 7029 shows expected threshold changes due purely to age for carefully screened populations (i.e. excluding those with ear disease, noise exposure etc.), based on a meta-analysis of published data.[5][6] Age affects high frequencies more than low, and men more than women. One early consequence is that even young adults may lose the ability to hear very high frequency tones above 15 or 16 kHz.[3] Despite this, age-related hearing loss may only become noticeable later in life. The effects of age can be exacerbated by exposure to environmental noise, whether at work or in leisure time (shooting, music, etc.). This is noise-induced hearing loss (NIHL) and is distinct from presbycusis. A second exacerbating factor is exposure to ototoxic drugs and chemicals.

Over time, the detection of high-pitched sounds becomes more difficult, and speech perception is affected, particularly of sibilants and fricatives. Patients typically express a decreased ability to understand speech. Once the loss has progressed to the 2–4 kHz range, there is increased difficulty understanding consonants. Both ears tend to be affected. The impact of presbycusis on communication depends on both the severity of the condition and the communication partner.[7]

Older adults with presbycusis often exhibit associated symptoms of social isolation, depression, anxiety, frailty and cognitive decline.[8] The risk of having cognitive impairment increased 7 percent for every 10 dB of hearing loss at baseline. No effect of hearing aids was seen in the Lin Baltimore study.[9]

Causes

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Changes in the inner ear, middle ear, and complex changes along the nerve pathways from the ear to the brain can affect hearing. Long-term exposure to noise and some medical conditions can also play a role. In addition, new research suggests that certain genes make some people more susceptible to hearing loss as they age.[10] Other risk factors include preexisting noise-induced hearing loss and exposure to ototoxic medications.[11]

Pathophysiology

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There are four pathological phenotypes of presbycusis:

  • Sensory: characterised by degeneration of the organ of Corti, the sensory organ for hearing. Located within the scala media, it contains inner and outer hair cells with stereocilia. The outer hair cells play a significant role in the amplification of sound. Age-related hair cell degeneration is characterized by loss of stereocilia, shrinkage of hair cell soma, and reduction in outer hair cell mechanical properties, suggesting that functional decline in mechanotransduction and cochlear amplification precedes hair cell loss and contributes to age-related hearing loss. At the molecular level, hair cell aging is associated with key molecular processes, including transcriptional regulation, DNA damage/repair, autophagy, and inflammatory response, as well as those related to hair cell unique morphology and function.[12] A 2020 study suggests that the main cause of presbycusis is the loss of inner ear sensory cellsand that the main cause of this loss is noise exposure. [13]
  • Neural: characterised by degeneration of cells of the spiral ganglion.
  • Strial/metabolic: characterised by atrophy of stria vascularis in all turns of cochlea. Located in the lateral wall of the cochlea, the stria vascularis contains sodium-potassium-ATPase pumps that are responsible for producing the endolymph resting potential. As individuals age, a loss of capillaries leads to the endolymphatic potential becoming harder to maintain, which brings a decrease in cochlear potential.
  • Cochlear conductive: due to stiffening of the basilar membrane thus affecting its movement. This type of pathology has not been verified as contributing to presbycusis.

In addition there are two other types:

  • Mixed
  • Indeterminate

The shape of the audiogram categorizes abrupt high-frequency loss (sensory phenotype) or flat loss (strial phenotype).

Classically, audiograms in neural presbycusis show a moderate downward slope into higher frequencies with a gradual worsening over time. A severe loss in speech discrimination is often described, out of proportion to the threshold loss, making amplification difficult due to poor comprehension.

The audiogram associated with sensory presbycusis is thought to show a sharply sloping high-frequency loss extending beyond the speech frequency range, and clinical evaluation reveals a slow, symmetric, and bilateral progression of hearing loss.[14]

Diagnosis

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Hearing loss is classified as mild, moderate, severe or profound. Pure-tone audiometry for air conduction thresholds at 250, 500, 1000, 2000, 4000, 6000 and 8000 Hz is traditionally used to classify the degree of hearing loss in each ear. Normal hearing thresholds are considered to be 25 dB sensitivity, though it has been proposed that this threshold is too high, and that 15 dB is more typical. Mild hearing loss is thresholds of 25–45 dB; moderate hearing loss is thresholds of 45–65 dB; severe hearing loss is thresholds of 65–85 dB; and profound hearing loss thresholds are greater than 85 dB.

Tinnitus occurring in only one ear should prompt the clinician to initiate further evaluation for other etiologies. In addition, the presence of a pulse-synchronous rushing sound may require additional imaging to exclude vascular disorders.

Otoscopy

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An examination of the external ear canal and tympanic membrane performed by a medical doctor, otolaryngologist, or audiologist using an otoscope, a visual instrument inserted into the ear. This also allows some inspection of the middle ear through the translucent tympanic membrane.

Tympanometry

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A test administered by a medical doctor, otolaryngologist or audiologist of the tympanic membrane and middle ear function using a tympanometer, an air-pressure/sound wave instrument inserted into the ear canal. The result is a tympanogram showing ear canal volume, middle ear pressure and eardrum compliance. Normal middle ear function (Type A tympanogram) with a hearing loss may suggest presbycusis. Type B and Type C tympanograms indicate an abnormality inside the ear and therefore may have an additional effect on the hearing.

Laboratory studies

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This may include a blood or other sera test for inflammatory markers such as those for autoinflammatory diseases.

Audiometry

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A hearing test administered by a medical doctor, otolaryngologist (ENT) or audiologist including pure tone audiometry and speech recognition may be used to determine the extent and nature of hearing loss, and distinguish presbycusis from other kinds of hearing loss. Otoacoustic emissions and evoked response testing may be used to test for audio neuropathy. The diagnosis of a sensorineural pattern hearing loss is made through audiometry, which shows a significant hearing loss without the "air-bone gap" that is characteristic of conductive hearing disturbances. In other words, air conduction is equal to bone conduction. Persons with cochlear deficits fail otoacoustic emissions testing, while persons with 8th cranial nerve (vestibulocochlear nerve) deficits fail auditory brainstem response testing.

Presbycusis audiogram

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Magnetic resonance imaging (MRI)

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As part of differential diagnosis, an MRI scan may be done to check for vascular anomalies, tumors, and structural problems like enlarged mastoids. MRI and other types of scan cannot directly detect or measure age-related hearing loss.

Treatment

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At present, presbycusis, being primarily sensorineural in nature, cannot be prevented, ameliorated or cured. Treatment options fall into three categories: pharmacological, surgical and management.

  • There are no approved or recommended pharmaceutical treatments for presbycusis.

Cochlear implant

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In cases of severe or profound hearing loss, a surgical cochlear implant is possible. This is an electronic device that replaces the cochlea of the inner ear. Electrodes are typically inserted through the round window of the cochlea, into the fluid-filled scala tympani. They stimulate the peripheral axons of the primary auditory neurons, which then send information to the brain via the auditory nerve. The cochlea is tonotopically mapped in a spiral fashion, with lower frequencies localizing at the apex of the cochlea, and high frequencies at the base of the cochlea, near the oval and round windows. With age, comes a loss in distinction of frequencies, especially higher ones. The electrodes of the implant are designed to stimulate the array of nerve fibers that previously responded to different frequencies accurately. Due to spatial constraints, the cochlear implant may not be inserted all the way into the cochlear apex. It provides a different kind of sound spectrum than natural hearing, but may enable the recipient to recognize speech and environmental sounds.

Middle ear implants

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These are surgically implanted hearing aids inserted onto the middle ear. These aids work by directly vibrating the ossicles, and are cosmetically favorable due to their hidden nature.

Management

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  • Hearing aids help improve hearing of many elderly. Hearing aids can now be tuned to specific frequency ranges of hearing loss.
  • Aural rehabilitation for the affected person and their communication partners may reduce the impact on communication. Techniques such as squarely facing the affected person, enunciating, ensuring adequate light, minimizing noise in the environment, and using contextual cues are used to improve comprehension.[7]
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Abilities of young people to hear high frequency tones inaudible to those over 25 or so has led to the development of technologies to disperse groups of young people around shops (The Mosquito), and development of a cell phone ringtone, Teen Buzz, for students to use in school, that older people cannot hear. In September 2006 this technique was used to make a dance track called 'Buzzin'.[15] The track had two melodies, one that everyone could hear and one that only younger people could hear.

Animals

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Many vertebrates such as fish, birds and amphibians do not experience presbycusis in old age as they are able to regenerate their cochlear sensory cells, whereas mammals including humans have genetically lost this ability.[16] A number of laboratories worldwide are conducting comparative studies of birds and mammals that aim to find the differences in regenerative capacity, with a view to developing new treatments for human hearing problems.[17]

See also

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  • Presbyopia – age-related degeneration of the eyes

References

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  1. ^ Online Etymology Dictionary, Presbycousis
  2. ^ Lee, Kyu-Yup (September 17, 2013). "Pathophysiology of Age-related Hearing loss (Peripheral and Central)". Korean Journal of Audiology. 17 (2): 45–49. doi:10.7874/kja.2013.17.2.45. PMC 3936539. PMID 24653905.
  3. ^ a b Rodriguez Valiente A, Trinidad A, Garcia Berrocal JR, Gorriz C, Ramirez Camacho R (April 2014). "Review: Extended high-frequency (9–20 kHz) audiometry reference thresholds in healthy subjects". Int J Audiol. 53 (8): 531–545. doi:10.3109/14992027.2014.893375. PMID 24749665. S2CID 30960789.
  4. ^ Education.com (23 May 2013). "Sonic Science: The High-Frequency Hearing Test". Scientific American. Retrieved 25 May 2017.
  5. ^ Robinson, DW; Sutton, GJ (1979). "Age effect in hearing – a comparative analysis of published threshold data". Audiology. 18 (4): 320–334. doi:10.1080/00206097909072634. PMID 475664.
  6. ^ Van Eyken, E.; Van Camp, G.; Van Laer, L. (2007). "The Complexity of Age-Related Hearing Impairment: Contributing Environmental and Genetic Factors". Audiology and Neurotology. 12 (6): 345–358. doi:10.1159/000106478. PMID 17664866. S2CID 35074115.
  7. ^ a b Huang, Qi; Tang, Jianguo (13 May 2010). "Age-related hearing loss or presbycusis". European Archives of Oto-Rhino-Laryngology. 267 (8): 1179–1191. doi:10.1007/s00405-010-1270-7. PMID 20464410. S2CID 45705548.
  8. ^ Jayakody, Dona M. P.; Friedland, Peter L.; Martins, Ralph N.; Sohrabi, Hamid R. (2018-03-05). "Impact of Aging on the Auditory System and Related Cognitive Functions: A Narrative Review". Frontiers in Neuroscience. 12: 125. doi:10.3389/fnins.2018.00125. ISSN 1662-4548. PMC 5844959. PMID 29556173.
  9. ^ Blazer, DG; Domnitz, S; Liverman, CT (6 September 2016). "Hearing Health Care for Adults: Priorities for Improving Access and Affordability". National Academies Press.
  10. ^ "Age-Related Hearing Loss (Presbycusis)". 17 March 2023.
  11. ^ "Presbycusis: When Age Affects Your Hearing".
  12. ^ Liu, Huizhan; Giffen, Kimberlee P; Chen, Lei; Henderson, Heidi J; Cao, Talia; Kozeny, Grant A; Beisel, Kirk W; Li, Yi; He, David Z (2022). "Molecular and cytological profiling of biological aging of mouse cochlear inner and outer hair cells". Cell Reports. 39 (110665): 110665. doi:10.1016/j.celrep.2022.110665. PMC 9069708. PMID 35417713.
  13. ^ Pei-zhe Wu, Jennifer T. O’Malley, Victor de Gruttola, M. Charles Liberman (2020-08-12), "Age-Related Hearing Loss Is Dominated by Damage to Inner Ear Sensory Cells, Not the Cellular Battery That Powers Them", Journal of Neuroscience, vol. 40, no. 33, pp. 6357–6366, doi:10.1523/JNEUROSCI.0937-20.2020, ISSN 0270-6474, PMC 7424870, PMID 32690619, retrieved 2023-11-11{{citation}}: CS1 maint: multiple names: authors list (link)
  14. ^ Fernández del Campo, Inés S.; Carmona-Barrón, Venezia G.; Diaz, I.; Plaza, I.; Alvarado, J. C.; Merchán, M. A. (2024-03-15). "Multisession anodal epidural direct current stimulation of the auditory cortex delays the progression of presbycusis in the Wistar rat". Hearing Research. 444: 108969. doi:10.1016/j.heares.2024.108969. ISSN 0378-5955. PMID 38350175.
  15. ^ "UK | Wales | South East Wales | Secret alarm becomes dance track". BBC News. 2006-09-26. Retrieved 2013-08-01.
  16. ^ Rubel, Edwin W.; Furrer, Stephanie A.; Stone, Jennifer S. (2013). "Review: A brief history of hair cell regeneration research and speculations on the future". Hearing Research. 297: 42–51. doi:10.1016/j.heares.2012.12.014. PMC 3657556. PMID 23321648.
  17. ^ Helen Briggs (20 September 2017). "Owls hold secret to ageless ears". BBC News. Retrieved 20 September 2017.
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