Age-related hearing loss
Learn about Age-related hearing loss, its reported features, relevant specialists, and questions to discuss at a medical consultation.
Also known as: Age-related hearing impairment; Deafness due to old age; Hearing loss, age-related; Old-aged sensorineural hearing impairment; Presbyacusia; Presbycusis
The sources compiled here do not cover: diagnosis, treatment, prevention, prognosis, onset. Ask the treating doctor about these.
What it is, symptoms and effects
From: MedlinePlus Genetics, National Library of Medicine
Age-related hearing loss (also known as presbycusis) is a decrease in hearing ability that happens with age. In most cases, the hearing loss affects both ears. It can begin as early as a person's thirties or forties and worsens gradually over time.
Age-related hearing loss first affects the ability to hear high-frequency sounds, such as speech. Affected people find it increasingly difficult to understand what others are saying, particularly when there is background noise (such as at a party). However, because the hearing loss is gradual, many people do not realize they cannot hear as well as they used to. They may turn up the television volume or start speaking louder without being aware of it.
As the hearing loss worsens, it affects more frequencies of sound, making it difficult to hear more than just speech. Determining where a sound is coming from (localization) and identifying its source become more challenging. Some affected individuals also experience a ringing sensation in the ears (tinnitus) or dizziness and problems with balance (presbystasis).
Age-related hearing loss often impacts a person's quality of life. Because affected individuals have trouble understanding speech, the condition affects their ability to communicate. It can contribute to social isolation, depression, and loss of self-esteem. Age-related hearing loss also causes safety issues if individuals become unable to hear smoke alarms, car horns, and other sounds that alert people to dangerous situations.
Causes and biological mechanisms
From: MedlinePlus Genetics, National Library of Medicine
The causes of age-related hearing loss are complex. This condition results from a combination of genetic, environmental, and lifestyle factors, many of which have not been identified. Age-related hearing loss is most commonly associated with changes in the inner ear, where sound waves are converted to nerve impulses that are sent to the brain. However, it can also be associated with nerve pathways that carry sound information in the brain or changes in the eardrum or in the small bones in the middle ear. In most cases, the exact cause of these changes is unknown.
Inherited variations in multiple genes likely influence whether age-related hearing loss occurs, the age at which it begins, and its severity. Some of these genes are important for the normal structure or function of the inner ear. Mutations in a subset of these genes also cause forms of nonsyndromic hearing loss that begin earlier in life. Other genes that have been studied in people with age-related hearing loss play roles in aging and other age-related diseases. It is unclear how variations in these genes contribute to age-related hearing loss.
Among the best-studied genetic factors associated with age-related hearing loss are changes in mitochondrial DNA (mtDNA). Mitochondria are structures within cells that convert the energy from food into a form that cells can use. Although most DNA is packaged in chromosomes within the nucleus, mitochondria also have a small amount of their own DNA. As people age, mtDNA accumulates damaging mutations, including deletions and other changes. This damage results from a buildup of harmful molecules called reactive oxygen species, which are byproducts of energy production in mitochondria. Damage to mtDNA causes cells to malfunction and ultimately to die. Cells that have high energy demands, such as those in the inner ear that are critical for hearing, are particularly sensitive to the effects of mtDNA damage. This damage can irreversibly alter the function of the inner ear, leading to hearing loss.
Environmental and lifestyle factors also contribute to age-related hearing loss. These factors include long-term exposure to loud noise (particularly through earphones at high volume), smoking, and exposure to heavy metals such as mercury or lead. In addition, certain medications (such as some antibiotics and chemotherapy drugs) can damage cells in the inner ear that are necessary for hearing. For reasons that are not fully understood, some health conditions that are common in older people, including heart disease and diabetes, also influence age-related hearing loss. Nutritional factors (for example, a shortage of certain vitamins or minerals) may also play a role, although the exact relationship between diet and hearing is unclear.
Inheritance and family implications
From: MedlinePlus Genetics, National Library of Medicine
Age-related hearing loss typically does not have a clear pattern of inheritance, although many affected individuals report a family history of the condition. Studies suggest that people who have close relatives with severe age-related hearing loss have an increased risk of developing severe hearing loss themselves as they age. However, it can be difficult to tell whether age-related hearing loss is inherited in a family because the condition is so common in the general population.
How common is it?
From: MedlinePlus Genetics, National Library of Medicine
Age-related hearing loss is one of the most common health conditions affecting older adults. Tens of millions of people worldwide are affected. In the United States, an estimated one-third of people over age 65, and half of those over 85, have some hearing loss.
Which doctor should you see?
The suggested department for discussing Age-related hearing loss is Clinical Genetics, with a clinical geneticist as the relevant type of clinician. Paediatrician (children) or physician (adults), with clinical geneticist referral.
This is an editorial referral starting point. The appropriate clinic depends on the person’s age, symptoms, previous diagnosis and local services. The first clinician can decide whether another specialty or a team is needed; a department label does not confirm the diagnosis.
How to prepare for an assessment
Bring a short timeline of the main symptoms: when they first appeared, whether they are constant or episodic, what seems to change them, and how they affect daily activities. Include previous reports, discharge summaries, current medicines and supplements, allergies, and any relevant family history. A dated record is more useful than trying to match every feature in an online article.
Ask the clinician what is already established and what remains uncertain. If a test is suggested, ask what question it answers, what its limitations are and how the result would change the next step. The information here is not an instruction to arrange every possible test. In children, bring growth, developmental and school information if it is relevant to the concern.
- Does the exact genetic or chromosome finding explain the observed features?
- Would a genetic counsellor help the family understand the result?
- Which organ-specific assessments are appropriate for this particular diagnosis?
Treatment discussions and follow-up
The material gathered for this draft does not provide a complete condition-specific treatment pathway for Age-related hearing loss. That gap does not mean that treatment is unavailable. A clinician needs to establish the diagnosis and review current guidance before recommending medicines, procedures, rehabilitation or other support.
Before leaving the appointment, clarify the next review date, who will communicate results, and whom to contact if the situation changes. Discuss difficulties with sleep, work, school, mobility, eating or emotional wellbeing when these are relevant. Practical support may require coordination between the treating clinician and other services.
The collected references do not establish a complete prevention or long-term outlook section for this entry. Missing information should not be interpreted as proof that prevention is impossible or that a particular outcome is inevitable. Ask what is known for the exact subtype, stage and personal circumstances, and which uncertainties remain.
When to seek emergency help
Severe breathing difficulty, collapse, new stroke-like symptoms, a seizure that is prolonged or repeated without recovery, uncontrolled major bleeding, or an immediate risk of self-harm require emergency help. In India, call 112 or reach the nearest emergency department. This is a general, non-exhaustive warning list; it is not a condition-specific triage tool.
This condition is usually assessed by a clinical geneticist. The Doctor Index does not list that speciality yet. A family physician or paediatrician can examine, arrange first tests and refer to the right specialist centre.
All clinical genetics conditions →
Sources
- MedlinePlus Genetics, National Library of Medicine — Age-related hearing loss — Public-domain Genetics summary
- Government of India — Emergency Response Support System — Official reference for India emergency number
Source: MedlinePlus, National Library of Medicine. Orphadata Science: Free access data from Orphanet. © INSERM 1999; July 2026 data, CC BY 4.0. This product uses the Human Phenotype Ontology (hp/releases/2026-09-01). Only sources listed for this article apply. Source material has been selected and arranged; HPO definitions are reproduced without alteration. No source organisation endorses this compilation. Köhler S et al. The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data. Nucleic Acids Research 2014;42(D1):D966–D974. doi:10.1093/nar/gkt1026.
General information, not advice about your situation. Errors can be reported through the corrections process. Reference TDI-C-0122.