Learning Center: HEARING

Access information in greater detail.

Use the search tool or scroll down for your topic of interest.


HEARING IS BRAIN HEALTH

Last reviewed: October 4, 2026

Introduction

Hearing loss is one of the most common health conditions in adults. Based on national hearing test data, about 23% of Americans age 12 and older have hearing loss in their better ear, and the proportion and severity rise steadily with age [1]. Most of this is gradual, age-related loss of the inner ear's hair cells, often added to by years of noise exposure. Only a minority of adults who could benefit from hearing aids use them [2].

This page covers why hearing matters for brain health, how the ear works, the types of hearing loss, sudden hearing loss (an emergency), hearing aids and cochlear implants, ear fluid, tinnitus and auditory processing disorder. A numbered reference list is at the end of the page.

Cognitive decline is well known to occur with age—mild for some, and more severe for others. A growing body of evidence now shows that hearing impairment accelerates cognitive decline. Fortunately, this process is modifiable in that improvement in hearing, such as with use of hearing aids, can significantly slow the rate of cognitive decline.

The 2024 report of the Lancet Commission on dementia identified 14 modifiable risk factors that together account for about 45% of dementia worldwide. Untreated hearing loss in midlife was one of the largest, accounting for an estimated 7% of dementia cases [3]. In a meta-analysis of observational studies including more than 125,000 people, hearing aid or cochlear implant users had a 19% lower risk of long-term cognitive decline than people with untreated hearing loss [4].

The best test so far is the ACHIEVE randomized trial of 977 adults aged 70 to 84 with untreated hearing loss. Over three years, a hearing intervention (audiologist-fitted hearing aids and counseling) did not slow cognitive decline in the group as a whole. However, among participants recruited from a long-running heart study, who were older and had more risk factors for dementia, the hearing intervention slowed cognitive decline by 48% [5]. This was a planned subgroup analysis, so it supports, but does not prove, a benefit for people at higher risk. Hearing aids clearly improve communication and quality of life regardless [6].


ANATOMY OF THE EAR

Anatomically, the ear is divided into three main components: the outer ear, the middle ear, and the inner ear.

The outer ear or external ear is the external part of the ear, which consists of the visible auricle (also pinna) and the ear canal. It gathers sound energy and focuses it on the eardrum (tympanic membrane).

The visible part is called the auricle or pinna. It is composed of a thin plate of cartilage, covered with skin, and connected to the surrounding parts by ligaments and muscles.

From the pinna, sound waves move into the ear canal (also known as the external acoustic meatus) a simple tube running through to the middle ear. This tube leads inward from the bottom of the auricula and conducts the vibrations to the tympanic cavity and amplifies frequencies in the range 3 kHz to 12 kHz.

The middle ear is the portion of the ear internal to the eardrum, and external to the inner ear. The mammalian middle ear contains three small bones (the ossicles—maleus, incus, and stapes), which transfer the vibrations of the eardrum into waves in the fluid and membranes of the inner ear. The hollow space of the middle ear is also known as the tympanic cavity and is surrounded by the tympanic part of the temporal bone. The Eustachian tube joins the tympanic cavity with the nasal cavity (more specifically, the nasopharynx), allowing pressure to equalize between the middle ear and throat.

The primary function of the middle ear is to efficiently transfer acoustic energy from compression waves in air to fluid–membrane waves within the cochlea.

The inner ear (internal ear, auris interna) is the innermost part of the vertebrate ear. In vertebrates, the inner ear is mainly responsible for sound detection and balance. In mammals, it consists of the bony labyrinth, a hollow cavity in the temporal bone of the skull with a system of passages comprising two main functional parts:

  • The cochlea, dedicated to hearing; converting sound pressure patterns from the outer ear into electrochemical impulses which are passed on to the brain via the auditory nerve.

  • The vestibular system, dedicated to balance

The inner ear conducts information to the brain via the eighth cranial nerve, which is really two nerves together, the acoustic nerve and the vestibular nerve, sometimes called the vestibuloacoustic nerve.


TYPES OF HEARING LOSS

The hearing mechanism converts sound waves into electrical signals that are input into the brain. Here is an excellent video from the National Institutes of Health briefly explaining the process. Any type of disruption of this process, anywhere from the outer ear to the brain leads to hearing loss. Conductive hearing loss is a category of hearing loss resulting from any impairment of the mechanical energy of sound traveling through the ear canal to the eardrum, through the three middle ear bones (ossicles). On the other hand, sensorineural hearing loss refers to any impairment of the cochlea (where the mechanical energy is converted to nerve signals) and the auditory nerve.

When both types are present, the loss is called mixed hearing loss. Common causes include:

  • Conductive: earwax blocking the canal, fluid behind the eardrum, a hole in the eardrum, cholesteatoma, and otosclerosis (stiffening of the stapes bone). Many conductive losses can be corrected with treatment or surgery.

  • Sensorineural: age-related hearing loss (presbycusis), noise exposure, inherited hearing loss, medications that damage the inner ear, Meniere's disease, sudden sensorineural hearing loss and, rarely, a tumor of the hearing nerve (acoustic neuroma). Sensorineural loss is usually permanent and is treated with hearing aids or, when severe, a cochlear implant.

A hearing test (audiogram) measures the softest sounds heard at each pitch, compares hearing through the ear canal with hearing through the bone to separate conductive from sensorineural loss, and tests understanding of words. Tympanometry measures how well the eardrum moves and detects fluid or pressure problems behind it (see the ear pressure page). Hearing loss is described by degree (mild, moderate, severe, profound). Most Americans with hearing loss have mild loss, but moderate loss becomes the most common degree after age 80 [1].


AN EMERGENCY: SUDDEN SENSORINEURAL HEARING LOSS

It is not usually clear to a patient (or their general physician) whether a sudden hearing loss is sensorineural or conductive. When in doubt, an otolaryngologist’s evaluation can differentiate the two. If the hearing loss is sensorineural, time is of the essence, and prompt diagnosis and treatment may prevent permanent hearing loss.

Sudden sensorineural hearing loss is a loss of at least 30 decibels over three consecutive pitches that develops within 72 hours, usually in one ear. It often is noticed on waking or when using the telephone, and it may come with tinnitus, ear fullness or dizziness. It affects an estimated 5 to 27 per 100,000 people each year, and in about 90% of cases no cause is found ("idiopathic") [7]. The American Academy of Otolaryngology–Head and Neck Surgery guideline makes these main statements [7]:

  • Distinguish sensorineural from conductive loss at the first visit (a tuning fork test can do this in the office), and obtain a hearing test promptly.

  • Evaluate for a cause such as an acoustic neuroma, usually with an MRI. A CT scan of the head is not recommended for routine evaluation, and routine blood tests are not recommended.

  • Corticosteroids (by mouth, by injection through the eardrum, or both) may be offered within two weeks of onset. The evidence for steroids as first treatment is not strong, partly because many patients recover on their own, but treatment is most likely to help when started early.

  • Intratympanic steroid injections should be offered as "salvage" treatment when recovery is incomplete two to six weeks after onset.

  • Hyperbaric oxygen therapy, combined with steroids, may be offered within two weeks of onset, or as salvage treatment within one month.

  • Antivirals, blood thinners, vasodilators and antioxidants are not recommended for routine use.

  • Counsel patients with permanent loss about hearing aids and other hearing rehabilitation.

Some recovery happens without treatment in an estimated 32% to 65% of patients, usually within two weeks [7]. Recovery is less likely with severe loss, dizziness, older age, and delay in treatment.

• Link to frequently asked questions and evidence-based answers on Sudden Sensorineural Hearing Loss on ENTHealth website.


HEARING AIDS

A hearing aid is a device designed to improve hearing by making sound audible to a person with hearing loss. Hearing aids are classified as medical devices in most countries, and regulated by the respective regulations. Small audio amplifiers such as Personal Sound Amplification Products (PSAPs) or other plain sound reinforcing systems are not designated as "hearing aids". PSAPs are mostly off-the-shelf amplifiers for people with normal hearing who need a little boost in volume in certain settings. Hearing aids contain a much higher level of technology prescribed to treat a diagnosed hearing loss. PSAPs are not regulated under the Food, Drug and Cosmetic Act because they are not intended to treat, diagnose or cure hearing impairment and do not alter the structure or function of the body. Modern hearing aid devices are computerized electroacoustic systems that transform environmental sound to make it audible, according to audiometric and cognitive rules. Modern devices also utilize sophisticated digital signal processing to try and improve speech intelligibility and comfort for the user. Such signal processing includes feedback management, wide dynamic range compression, directionality, frequency lowering, and noise reduction.

Modern hearing aids require configuration to match the hearing loss, physical features, and lifestyle of the wearer. The hearing aid is fitted to the most recent audiogram (hearing test) and is programmed by frequency. This process is called "fitting" and is performed by a Doctor of Audiology, also called an audiologist (AuD), or by a Hearing Instrument Specialist (HIS). The amount of benefit a hearing aid delivers depends in large part on the quality of its fitting

Hearing aids help. In a Cochrane review of randomized trials in adults with mild to moderate hearing loss, hearing aids produced large improvements in listening ability and in hearing-related quality of life (how much hearing loss limits daily activities and relationships) compared with no hearing aids [6]. Even so, only about 1 in 7 Americans age 50 and older with hearing loss uses hearing aids [2]. Common reasons are cost, stigma, and the belief that the loss is not bad enough.

Since 2022, the U.S. Food and Drug Administration has allowed over-the-counter (OTC) hearing aids for adults with perceived mild to moderate hearing loss, sold without a prescription or hearing test. In a randomized trial of 64 adults, a self-fitted OTC hearing aid with remote support gave results similar to an audiologist-fitted hearing aid after six weeks [8]. OTC aids are a reasonable option for many people with mild to moderate loss. A medical evaluation and hearing test are still recommended first if the loss is sudden, worse in one ear, accompanied by ear pain, drainage, dizziness or tinnitus in one ear, or more than moderate, because these point to problems hearing aids alone do not address.


COCHLEAR IMPLANT

A cochlear implant (CI) is a surgically implanted neuroprosthetic device to provide a person with moderate to profound sensorineural hearing loss a modified sense of sound. CI bypasses the normal acoustic hearing process to replace it with electric signals which directly stimulate the auditory nerve. A person with a cochlear implant receiving intensive auditory training may learn to interpret those signals as sound and speech.

The implant has two main components. The outside component is generally worn behind the ear, but could also be attached to clothing, for example, in young children. This component, the sound processor, contains microphones, electronics that include Digital Signal Processor chips, battery, and a coil which transmits a signal to the implant across the skin. The inside component, the actual implant, has a coil to receive signals, electronics, and an array of electrodes which is placed into the cochlea, which stimulate the cochlear nerve.

The surgical procedure is performed under general anesthesia. Surgical risks are minimal but can include tinnitus, facial nerve injury (temporary or permanent) and dizziness.

From the early days of implants in the 1970s and the 1980s, speech perception via an implant has steadily increased. Many users of modern implants gain reasonable to good hearing and speech perception skills post-implantation, especially when combined with lipreading. One of the challenges that remain with these implants is that hearing and speech understanding skills after implantation show a wide range of variation across individual implant users. Factors such as duration and cause of hearing loss, how the implant is situated in the cochlea, the overall health of the cochlear nerve, but also individual capabilities of re-learning are considered to contribute to this variation, yet no certain predictive factors are known.

Cochlear implants are considered when hearing aids no longer provide enough speech understanding. In a systematic review of 42 studies of adults, a cochlear implant in one ear produced significant improvement in understanding speech and in quality of life, and implants in both ears added better ability to tell where sounds come from [9]. An international consensus panel concluded that implantation is the standard of care for adults with severe to profound hearing loss who get limited benefit from hearing aids, that candidacy has widened over time to include people with some remaining hearing, and that cochlear implants remain underused [10]. Testing for candidacy includes a hearing test with word and sentence understanding while wearing well-fitted hearing aids, imaging of the inner ear, and counseling about expectations and rehabilitation.


• Link to Understanding Ear Fluid (and how it is different from infection) on the ENTHealth website. (My rating: C)

• Link to Treating and Managing Ear Fluid on theENTHealth website. (My rating: B)

• Link to evidence-based information on speech and language development in children as it relates to ear fluid. (My rating: A)

Ear fluid (otitis media with effusion) causes a temporary conductive hearing loss, and in adults fluid in only one ear deserves an examination of the back of the nose. Causes and treatment, including ear tubes, are covered on the ear infections and ear pressure pages.


Tinnitus is the perception of sound when no corresponding external sound is present. While often described as a ringing, it may also sound like a clicking, buzzing, hiss, or roaring. Tinnitus is usually, but not always associated with hearing loss, and may be considered as a low signal-to-noise ratio from the ears.

Tinnitus may have no cure, but there are several treatments for this vexing problem. In brief, distracting noise (such as “white noise"), use of hearing aids, getting good sleep, getting daily exercise, and avoiding known dietary triggers (caffeine, ibuprofen and similar medications, apple cider vinegar, among others), alcohol, avoiding topical causes (sunscreen), and even cognitive behavioral therapy may help. Of course, prevention of tinnitus or its progression is important, and this is accomplished by avoiding excessive noise exposure and avoiding medications that hurt the inner ear (such as certain malaria medications and intravenous antibiotics called aminoglycosides).

• “How Can I Lessen the Impact of Tinnitus” at ENTHealth.org.

• Tinnitus information and resources from the American Speech and Language Association

Tinnitus is covered in detail, with references, on the tinnitus page.


Auditory Processing Disorder

Auditory processing disorder (APD), rarely known as King-Kopetzky syndrome or auditory disability with normal hearing (ADN), is an umbrella term for a variety of disorders that affect the way the brain processes auditory information. Individuals with APD usually have normal structure and function of the outer, middle, and inner ear (peripheral hearing). However, they cannot process the information they hear in the same way as others do, which leads to difficulties in recognizing and interpreting sounds, especially the sounds composing speech. It is thought that these difficulties arise from dysfunction in the brain.

The American Academy of Audiology notes that APD is diagnosed by difficulties in one or more auditory processes known to reflect the function of the brain. It can affect both children and adults. Its prevalence is currently estimated to be 2–7% in children in US and UK populations. APD can continue into adulthood. Cooper and Gates (1991) estimated the prevalence of adult APD to be 10 to 20%. It has been reported that males are twice as likely to be affected by the disorder as females, and that prevalence is higher in the elderly and increases with age.

The figure for adults comes from the Framingham study, where tests of central auditory processing were abnormal in a substantial share of older participants and the rate rose with age [11]. Prevalence estimates vary widely because there is no single agreed test or definition. A systematic review of children diagnosed with APD found that their difficulties were often not limited to hearing, but also involved attention, language and memory, which is why evaluation usually involves an audiologist together with speech-language and educational specialists [12]. Management focuses on improving the listening environment (reducing background noise, preferential seating, remote microphone systems) and on auditory training.

Related pages on this site: hearing loss, hearing treatments, make the most of your hearing loss appointment, Osia bone conduction implant, tinnitus, dizziness, ear pressure and ear infections.

Summary

  • About a quarter of Americans have some hearing loss, and it becomes more common and more severe with age [1].

  • Untreated hearing loss is one of the largest modifiable risk factors for dementia. Hearing treatment improves communication and quality of life, and may slow cognitive decline in people at higher risk [3, 5, 4].

  • Sudden hearing loss in one ear is an emergency: early evaluation and steroid treatment within two weeks give the best chance of recovery [7].

  • Hearing aids provide large benefits but are underused; over-the-counter aids are an option for mild to moderate loss [6, 2, 8].

  • Cochlear implants substantially improve speech understanding when hearing aids are no longer enough [9, 10].

References

  1. Goman AM, Lin FR. Prevalence of Hearing Loss by Severity in the United States. Am J Public Health. 2016;106(10):1820-2. doi:10.2105/AJPH.2016.303299 PubMed 27552261

  2. Chien W, Lin FR. Prevalence of hearing aid use among older adults in the United States. Arch Intern Med. 2012;172(3):292-3. doi:10.1001/archinternmed.2011.1408 PubMed 22332170

  3. Livingston G, Huntley J, Liu KY, et al. Dementia prevention, intervention, and care: 2024 report of the Lancet standing Commission. Lancet. 2024;404(10452):572-628. doi:10.1016/S0140-6736(24)01296-0 PubMed 39096926

  4. Yeo BSY, Song HJJMD, Toh EMS, et al. Association of Hearing Aids and Cochlear Implants With Cognitive Decline and Dementia: A Systematic Review and Meta-analysis. JAMA Neurol. 2023;80(2):134-141. doi:10.1001/jamaneurol.2022.4427 PubMed 36469314

  5. Lin FR, Pike JR, Albert MS, et al. Hearing intervention versus health education control to reduce cognitive decline in older adults with hearing loss in the USA (ACHIEVE): a multicentre, randomised controlled trial. Lancet. 2023;402(10404):786-797. doi:10.1016/S0140-6736(23)01406-X PubMed 37478886

  6. Ferguson MA, Sarant JZ, Bennett RJ, et al. Hearing aids for mild to moderate hearing loss in adults. Cochrane Database Syst Rev. 2026;8(8):CD012023. doi:10.1002/14651858.CD012023.pub3 PubMed 42644645

  7. Chandrasekhar SS, Tsai Do BS, Schwartz SR, et al. Clinical Practice Guideline: Sudden Hearing Loss (Update). Otolaryngol Head Neck Surg. 2019;161(1_suppl):S1-S45. doi:10.1177/0194599819859885 PubMed 31369359

  8. De Sousa KC, Manchaiah V, Moore DR, et al. Effectiveness of an Over-the-Counter Self-fitting Hearing Aid Compared With an Audiologist-Fitted Hearing Aid: A Randomized Clinical Trial. JAMA Otolaryngol Head Neck Surg. 2023;149(6):522-530. doi:10.1001/jamaoto.2023.0376 PubMed 37052929

  9. Gaylor JM, Raman G, Chung M, et al. Cochlear implantation in adults: a systematic review and meta-analysis. JAMA Otolaryngol Head Neck Surg. 2013;139(3):265-72. doi:10.1001/jamaoto.2013.1744 PubMed 23429927

  10. Buchman CA, Gifford RH, Haynes DS, et al. Unilateral Cochlear Implants for Severe, Profound, or Moderate Sloping to Profound Bilateral Sensorineural Hearing Loss: A Systematic Review and Consensus Statements. JAMA Otolaryngol Head Neck Surg. 2020;146(10):942-953. doi:10.1001/jamaoto.2020.0998 PubMed 32857157

  11. Cooper JC Jr, Gates GA. Hearing in the elderly--the Framingham cohort, 1983-1985: Part II. Prevalence of central auditory processing disorders. Ear Hear. 1991;12(5):304-11. doi:10.1097/00003446-199110000-00002 PubMed 1783233

  12. de Wit E, Visser-Bochane MI, Steenbergen B, et al. Characteristics of Auditory Processing Disorders: A Systematic Review. J Speech Lang Hear Res. 2016;59(2):384-413. doi:10.1044/2015_JSLHR-H-15-0118 PubMed 27082630



Learning Center Main Index:


 

This page