Psoriatic Arthritis
Pathophysiology and epidemiology
- A type of peripheral spondyloarthritis. Spondyloarthritis (SpA) is a group of autoimmune conditions involving arthritis (primarily enthesitis, where tendon meets bone) and extra-articular manifestations. SpA can be axial – primarily affecting the spine – or peripheral (psoriatic, reactive, or enteropathic), though both may have features of the other.
- Affects around 15% of people with psoriasis, and may present before skin signs.
Presentation
- Asymmetric oligoarthritis: commonest pattern.
- Symmetrical polyarthritis, similar to RA. Also common.
- Sacroiliitis, similar to ankylosing spondylitis.
- DIP joint disease.
- Arthritis mutilans: joint deformity and destruction.
Signs:
- Dactylitis: sausage fingers or toes.
- Onycholysis: distal nail detachment, preceded by yellow/brown discolouration.
- Nail pitting. Usually on same finger as DIP swelling; DIP swelling without nail changes is more characteristic of nodal osteoarthritis.
Risk factors
- Family history of psoriasis and/or SpA.
- Association with other autoimmune diseases: psoriasis, IBD, uveitis.
Investigations
- X-ray: DIP erosion leading to 'pencil-in-cup' appearance. If X-ray normal, consider US and/or MRI of affected sites.
- ↑ESR, ↑CRP.
- HLA-B27 (60-90% sensitive) may help support the diagnosis.
Management
- Oligo- or polyarthritis is managed essentially like rheumatoid arthritis (RA): cDMARDs → combination cDMARDs → bDMARDs (anti-TNFα then ustekinumab [anti-IL12 and IL-23]). NSAIDs can be used as an adjunct.
- Monoarthritis can initially be treated with local steroid injections.
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