Correlation Between Inflammatory Bowel Disease and Uveitis/Eye Symptoms
Ocular manifestations occur in 4-12% of patients with inflammatory bowel disease (IBD), with uveitis, episcleritis, and scleritis being the most clinically significant extra-intestinal manifestations that require prompt recognition and ophthalmologic referral to prevent vision loss. 1
Epidemiology and Prevalence
- The reported incidence of ocular manifestations ranges from 4-12% of IBD cases, though some tertiary center cohorts report rates as high as 29% (likely overestimates due to referral bias). 1
- Patients with IBD are significantly more likely to experience ocular symptoms compared to controls, even in community-based studies. 1
- Ocular involvement is more prevalent in Crohn's disease than ulcerative colitis, particularly for episcleritis. 2, 3
- In a recent cohort study, 3.7% of IBD patients had confirmed ocular extra-intestinal manifestations, with inflammatory surface pathologies (33.2%) and uveitis (14.9%) being most common. 4
Pathophysiology
Ocular manifestations represent diverse immune-mediated pathologies involving activation and infiltration of both innate and adaptive immune cells into ocular tissues. 1
- Genetic associations include NOD2 mutations and MICA on MHC class I, supporting innate immune activation in uveitis pathogenesis. 1
- In severe cases, scleritis may be associated with fibrinoid necrosis and vasculitis. 1
Specific Ocular Manifestations
Episcleritis
- Episcleritis is the most common ocular extra-intestinal manifestation of IBD and typically correlates with bowel disease activity. 5, 3
- Clinical presentation includes mild or no pain, hyperemia of superficial conjunctival and episcleral vessels, itching, and burning sensation without visual changes. 1, 5
- Episcleritis may self-resolve and often responds to management of the underlying bowel disease. 1
Uveitis
- Uveitis is less common but has potentially more severe consequences, including risk of permanent vision loss. 1
- When related to Crohn's disease, uveitis is frequently bilateral, insidious in onset, and long-lasting. 1, 6
- Classical symptoms include eye pain, blurred vision, photophobia, and headache. 1, 6
- Critical distinction: Unlike episcleritis, uveitis can occur independently of bowel disease activity and may even precede the onset of intestinal symptoms. 1, 7
Scleritis
- Scleritis presents with severe pain, deep vessel involvement, and potential vision loss, distinguishing it from the milder episcleritis. 5, 8
- Visual disturbance, photophobia, or moderate to severe pain should prompt urgent ophthalmologic referral. 1, 6
Clinical Approach and Red Flags
When to Suspect Ocular Involvement
- Any IBD patient complaining of eye symptoms warrants careful evaluation, as symptoms are often nonspecific. 6, 7
- Episcleritis often occurs during IBD flares, while uveitis presents independently of intestinal disease activity. 1, 5, 3
Urgent Referral Criteria
Immediate ophthalmologic referral is required for:
- Visual disturbance or blurred vision 1, 6
- Photophobia 1
- Moderate to severe eye pain (suggests scleritis or uveitis, not episcleritis) 1, 5
- Any concern for uveitis or scleritis, as progression to permanent vision loss can occur without prompt treatment. 6, 8
Diagnostic Evaluation
- Slit-lamp examination by an ophthalmologist is essential to confirm diagnosis and differentiate between anterior and posterior uveitis, episcleritis, and scleritis. 1
- For uveitis, both the SUN guidelines and International Uveitis Study Group (IUSG) criteria are useful for disease classification. 1
Treatment Approach
Episcleritis
- Topical or systemic NSAIDs or topical corticosteroids can be used for symptomatic treatment. 1
- Treatment of the underlying bowel disease is the primary approach, as episcleritis often resolves with IBD control. 1
Uveitis
- Anterior uveitis should be treated with topical corticosteroids and cycloplegics. 1
- Treatment must be guided by an ophthalmologist with expertise in ocular inflammation. 1
- For refractory uveitis, systemic corticosteroids, conventional immunosuppressants, or anti-TNF agents are indicated. 1
Scleritis
- Scleritis requires systemic treatment including topical or systemic corticosteroids, conventional immunosuppressants, and anti-TNF agents. 1
- For necrotizing scleritis or refractory cases, immediate high-dose systemic corticosteroids plus disease-modifying antirheumatic drugs (DMARDs) are required. 8
- Anti-TNF agents (infliximab or adalimumab) are recommended when conventional DMARDs fail or for severe necrotizing scleritis. 8
Common Pitfalls
- Do not dismiss mild eye symptoms as insignificant—even episcleritis warrants evaluation and may indicate IBD flare. 5, 3
- Do not confuse episcleritis with scleritis—the presence of severe pain immediately raises concern for scleritis, which requires urgent systemic treatment. 5, 8
- Do not delay ophthalmologic referral for suspected uveitis or scleritis—these conditions can progress rapidly to permanent vision loss. 6, 8
- Be aware of iatrogenic ocular complications: corticosteroids may cause cataracts and glaucoma, while methotrexate can cause conjunctivitis and blepharitis. 9
- Recognize that anti-TNF agents, while effective for both IBD and uveitis, may paradoxically increase the risk of acute uveitis flares in some patients. 9