About this trial
Psoriatic arthritis (PsA) is an inflammatory joint disease that can also affect the liver. Some medications used to treat PsA, such as biological agents (TNF-alpha inhibitors and IL-17 inhibitors), may influence liver health over the long term. This retrospective study aims to evaluate the presence and progression of liver fibrosis (scarring) and hepatic steatosis (fatty liver) in PsA patients treated with TNF-alpha inhibitors or IL-17 inhibitors.
The study includes PsA patients who have used biological medications continuously for at least 2 years. Patients' liver health will be assessed using non-invasive tests such as liver ultrasonography and validated biochemical scoring systems (FIB-4, APRI). The findings will be compared with PsA patients treated only with methotrexate (MTX), a commonly used medication known to affect liver health.
This study will help understand whether biological therapies (TNF or IL-17 inhibitors) have a positive or negative impact on liver health compared to traditional treatments (MTX) in patients with psoriatic arthritis.
Eligibility criteria
Qualifiers
Age 18 to 65 years
Diagnosed with psoriatic arthritis (PsA) according to standard classification criteria
Receiving biologic therapy (anti-TNF or anti-IL-17) or MTX monotherapy for ≥2 years
Able to provide historical data (medical records) on liver ultrasound and laboratory parameters
Disqualifiers
History of any other chronic liver disease (e.g., viral hepatitis, autoimmune hepatitis)
Significant alcohol consumption (>20 g/day women, >30 g/day men)
Concomitant use of other hepatotoxic drugs apart from MTX
Unwillingness or inability to comply with study assessments
Trial design
Treatments tested in this trial
- Not listed