Can Psoriasis Cause Hearing Loss?

Psoriasis is a chronic, immune-mediated disorder primarily recognized for its effects on the skin, characterized by the rapid buildup of skin cells that leads to scaling and inflammation. Although often viewed as a localized dermatological disease, this condition affects the entire body. The underlying systemic inflammation allows it to extend its reach beyond the skin, potentially impacting various organ systems, including the auditory system. Research into these extracutaneous manifestations confirms a statistically significant association between the inflammatory processes of psoriasis and an increased risk of hearing impairment.

The Established Link Between Psoriasis and Hearing Impairment

Numerous epidemiological studies and meta-analyses have established a clear correlation between a psoriasis diagnosis and a higher prevalence of hearing difficulties compared to the general population. Individuals with psoriasis show elevated mean hearing thresholds across nearly all tested frequencies. This effect is noticeable in the higher frequency ranges, which are often the first to be affected by inner ear damage.

The association is linked to the severity and duration of the condition, suggesting chronic inflammatory insult over time. Patients with psoriasis have been found to have significantly increased odds for developing sensorineural hearing loss. Furthermore, the risk of experiencing sudden sensorineural hearing loss is notably higher for those with psoriasis.

The presence of Psoriatic Arthritis (PsA), a form of inflammatory arthritis associated with psoriasis, further elevates the risk of hearing impairment. This indicates that a greater systemic inflammatory burden contributes to auditory complications. The link is a consequence of the ongoing, body-wide inflammatory state characteristic of psoriasis, not external skin plaques alone.

Understanding the Mechanisms of Damage

The connection between psoriasis and auditory damage is rooted in the body’s overactive immune response and systemic inflammation. Psoriasis involves the activation of immune cells, such as T helper cells, which release high concentrations of pro-inflammatory mediators like tumor necrosis factor-alpha (TNF-alpha) and various interleukins. These circulating inflammatory molecules travel through the bloodstream and reach the inner ear.

The inner ear relies on a precise blood supply through a specialized microvasculature. Systemic inflammation makes these small blood vessels vulnerable to damage, a process known as vasculitis. Pro-inflammatory cytokines can induce vasospasm, the sudden constriction of these vessels, which severely limits blood flow to the cochlea. This oxygen deprivation, or ischemia, can damage or destroy the sensitive hair cells and neurons responsible for converting sound waves into electrical signals.

This systemic vascular hypothesis explains the observed sensorineural damage, as cochlear structures are highly susceptible to even brief periods of reduced blood flow. The autoimmune component of psoriasis may also play a role through cross-reactivity. It is theorized that the immune system, while targeting skin cells, may mistakenly identify similar protein structures within the cochlea as foreign, leading to an immune attack on the inner ear itself.

Manifestations in the Ear and Types of Hearing Loss

Hearing impairment associated with psoriasis can manifest in two distinct ways, reflecting damage to different parts of the auditory pathway. The most common type linked to the systemic disease is sensorineural hearing loss (SNHL), which results from damage to the inner ear, specifically the cochlea or the auditory nerve. This type of loss is generally permanent and is believed to be a direct consequence of the inflammatory and vascular mechanisms that cause inner ear cell death.

A more acute manifestation is sudden sensorineural hearing loss (SSNHL), which involves the rapid onset of deafness, typically in one ear, over a period of three days or less. This sudden event is thought to be triggered by a rapid, immune-mediated inflammatory attack or vascular event within the cochlea.

Psoriasis can also cause conductive hearing loss, which involves a physical obstruction of sound transmission to the inner ear.

Psoriatic plaques can develop within the external ear and the lining of the ear canal. The rapid turnover and shedding of skin cells characteristic of psoriasis can lead to a buildup of scales and dead skin, physically blocking the passage of sound.

In patients who also have Psoriatic Arthritis, inflammation may affect the tiny joints (ossicles) in the middle ear, further interfering with sound conduction and contributing to a mixed hearing loss.

Monitoring and Management Considerations

Given the established link, proactive monitoring of auditory health is advisable for individuals with moderate to severe psoriasis. Recognizing early warning signs includes symptoms such as a feeling of fullness in the ear, the onset of ringing or buzzing (tinnitus), or any sudden, unexplained change in hearing ability. A sudden deterioration in hearing should be treated as a medical urgency, as prompt treatment may improve outcomes.

Patients with psoriasis should discuss the possibility of routine audiometric screening with their healthcare providers, even if they are not currently experiencing symptoms. Audiograms provide an objective measure of hearing thresholds and can detect high-frequency loss before it becomes noticeable in daily conversation. Early detection allows for timely intervention and management.

Treating the underlying systemic inflammation of psoriasis can have a beneficial effect on mitigating the risk of auditory complications. Systemic therapies, particularly biologics that target specific inflammatory pathways, may help protect the delicate inner ear structures from chronic inflammatory damage. Management of existing hearing loss may involve hearing aids, but this should occur in coordination with the dermatologist and rheumatologist to ensure that systemic disease activity is also well-controlled.