Can Arthritis Affect Your Eyes?

Arthritis is commonly perceived as a disease confined to the joints, causing pain and stiffness only in the body’s limbs. This perspective overlooks the fundamental nature of the condition, which is a malfunction of the immune system leading to chronic, systemic inflammation. Because inflammatory arthritis is a whole-body process, it can affect many organs far removed from the joints, including the eyes. The connection exists because the immune cells and inflammatory molecules that attack the joint linings can circulate and target structures within the eye.

Systemic Arthritis Types That Affect Vision

The risk of eye involvement differs significantly depending on the specific form of arthritis a person has been diagnosed with. Rheumatoid Arthritis (RA) is one of the most common types and frequently causes ocular issues, often manifesting as severe dry eye. The underlying inflammation in RA can also lead to more serious conditions that affect the outer layers of the eye. Individuals with RA who test positive for anti-cyclic citrullinated peptide (anti-CCP) antibodies or rheumatoid factor are statistically more likely to experience these eye-related complications.

A group of conditions known as Spondyloarthropathies, which includes Ankylosing Spondylitis (AS) and Psoriatic Arthritis (PsA), carry a distinct and significant risk of acute eye inflammation. Ankylosing Spondylitis has a particularly strong association with recurrent eye problems, with up to 33% of patients experiencing an episode of ocular inflammation at some point. This link is often tied to the presence of the human leukocyte antigen B27 (HLA-B27) gene, a common marker in both the systemic disease and the eye condition. Psoriatic Arthritis, which combines joint inflammation with skin disease, also increases the likelihood of developing certain eye issues, including inflammation of the middle layer of the eye.

Juvenile Idiopathic Arthritis (JIA) represents a high-risk category, especially for children who have the oligoarticular subtype, affecting four or fewer joints. Inflammation in JIA-associated eye disease is often chronic and can be particularly insidious because it frequently presents without noticeable symptoms in its early stages. This asymptomatic nature means that regular, prophylactic screening is absolutely necessary to detect the inflammation before it causes permanent damage. The severity and type of eye complication correlate with the underlying systemic disease activity and duration.

Distinct Ocular Conditions Triggered by Arthritis

The inflammation caused by arthritis can damage different parts of the eye, resulting in three primary categories of conditions. Keratoconjunctivitis Sicca (Severe Dry Eye) is the most frequent manifestation of arthritis-related eye disease, particularly affecting individuals with Rheumatoid Arthritis. This occurs when inflammation targets the tear-producing glands, leading to reduced tear production and chronic dryness that can damage the cornea and conjunctiva. Up to 40% of RA patients may experience this form of severe dry eye, which is often an overlap with secondary Sjögren’s syndrome.

Scleritis is a more severe, potentially sight-threatening condition involving the sclera, the tough, white outer layer of the eyeball. This deep inflammation is most commonly associated with RA and manifests as deep, constant, boring pain that can sometimes wake a patient from sleep. The sclera and cornea are composed largely of collagen and proteoglycans, similar to joint tissues, making them susceptible to the same autoimmune attack. Scleritis can lead to thinning of the sclera or cornea, and in its most destructive form, necrotizing scleritis, it can be a warning sign of systemic vasculitis.

A milder condition, Episcleritis, involves only the thin layer of tissue covering the sclera and typically presents as a red, mildly uncomfortable eye that often resolves on its own. Unlike scleritis, episcleritis is usually not associated with serious vision loss, but recurrent episodes may still indicate an underlying systemic inflammatory condition.

Uveitis is the third main condition and involves inflammation of the uvea, the middle layer of the eye that contains the iris, ciliary body, and choroid. Because the uvea is rich in blood vessels, it serves as a gateway for immune cells and inflammatory factors to enter the eye.

Uveitis is the most common eye problem in AS and JIA, and it is considered the most sight-threatening of the arthritis-related eye conditions. The acute, anterior form, affecting the iris, is the most common presentation in AS, causing sudden pain and light sensitivity. If left uncontrolled, chronic inflammation from uveitis can lead to secondary complications, including cataracts, glaucoma, and permanent vision loss from structural damage. The presence of inflammation in the eye often signals active systemic disease that requires aggressive management by a specialist.

Recognizing Symptoms and Coordinated Care

Patients with any form of inflammatory arthritis need to be aware of certain ocular symptoms that require immediate medical evaluation:

  • Persistent redness in the eye that does not improve with simple over-the-counter drops.
  • Deep, aching pain in the eye, particularly if it is severe or disrupts sleep, strongly suggesting a serious condition like scleritis.
  • Sudden change in vision or increased light sensitivity.
  • The appearance of new floaters.

For individuals diagnosed with high-risk forms of arthritis, such as JIA or AS, proactive and regular monitoring by an ophthalmologist is standard practice. These baseline and routine eye examinations are designed to detect inflammation early, often before the patient experiences any symptoms, which is particularly true for JIA-associated uveitis. Early detection allows for prompt treatment, which is the best defense against vision loss and long-term ocular damage.

Effective management of arthritis-related eye complications requires a highly coordinated approach between the patient’s rheumatologist and an ophthalmologist. The rheumatologist manages the underlying systemic inflammation using medications like disease-modifying antirheumatic drugs, which in turn helps control the eye condition. Meanwhile, the ophthalmologist focuses on localized treatment, such as steroid eye drops, and monitors for structural complications. Studies have shown that patients receiving this multidisciplinary care experience better overall outcomes, including a higher rate of disease control and fewer complications.