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Psoriatic disease--from skin to bone
1University of Rochester School of Medicine and Dentistry, 601 Elmwood Avenue, Box 695, Rochester, NY 14642, USA. christopher_ritchlin@urmc.rochester.edu
Nature Clinical Practice. Rheumatology
|November 27, 2007
Summary
Psoriatic arthritis is a complex inflammatory joint disease. Research highlights the significant role of monocyte-macrophages in its development, distinct from T lymphocytes, and links it to cardiovascular issues.
Area of Science:
- Rheumatology and Immunology
- Dermatology
Background:
- Psoriatic arthritis (PsA) is a heterogeneous inflammatory joint disease.
- Distinguishing PsA from other spondyloarthropathies relies on clinical, histopathologic, immunogenetic, and imaging data.
- Historically, T lymphocytes were considered primary drivers, but emerging evidence points to monocyte-macrophages.
Purpose of the Study:
- To differentiate psoriatic arthritis from rheumatoid arthritis and other spondyloarthropathies.
- To elucidate the role of monocyte-macrophages in psoriatic arthritis pathogenesis.
- To explore the relationship between psoriatic disease manifestations and adverse cardiovascular/metabolic outcomes.
Main Methods:
- Analysis of clinical features, histopathology, immunogenetics, and musculoskeletal imaging.
- Investigation of the cellular players in joint and skin inflammation.
- Examination of genetic risk factors and patient outcomes.
Main Results:
- Psoriatic arthritis exhibits distinct characteristics from other spondyloarthropathies.
- Monocyte-macrophages play a crucial role in initiating and sustaining inflammation in psoriatic arthritis.
- Psoriatic arthritis can occur without skin psoriasis, indicating distinct disease pathways.
- Adverse cardiovascular and metabolic outcomes may be linked to inflammatory pathways involving monocytes and macrophages.
Conclusions:
- Psoriatic arthritis is a distinct entity from psoriatic skin disease.
- The term 'psoriatic disease' now encompasses systemic inflammation affecting joints, eyes, and gut.
- Activated monocytes and macrophages contribute to systemic inflammation and associated comorbidities in psoriatic disease.
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