Bezmialem Vakif University
Istanbul, Fatih, 34093, Turkey (Türkiye)
Location contact
Mehmet Serkan Kılıçoğlu, MD
CONTACT
Mehmet Serkan Kılıçoğlu, MD
PRINCIPAL_INVESTIGATOR
Safa El Mardi Alaoui, MD
CONTACT
Safa El Mardi Alaoui, MD
SUB_INVESTIGATOR
NCT Number: NCT06918886
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.
Trial opening soon.
Get Notified18 year–65 year
All sexes
Observational
Istanbul, Fatih, 34093, Turkey (Türkiye)
Mehmet Serkan Kılıçoğlu, MD
CONTACT
Mehmet Serkan Kılıçoğlu, MD
PRINCIPAL_INVESTIGATOR
Safa El Mardi Alaoui, MD
CONTACT
Safa El Mardi Alaoui, MD
SUB_INVESTIGATOR
This is a retrospective, single-center observational study, conducted in the Physical Medicine and Rehabilitation Clinic, designed to assess the impact of long-term biologic therapy on liver health in patients with psoriatic arthritis (PsA). Participants must have received either TNF-alpha inhibitors or IL-17 inhibitors for at least two consecutive years. A separate group of PsA patients who have only received methotrexate (MTX) for at least two years will serve as a comparison cohort.
Objectives:
To estimate the frequency of hepatic steatosis and fibrosis using liver ultrasonography and validated biochemical scoring indices (FIB-4, APRI) among patients on biologic therapy and MTX.
To compare changes in fibrotic markers between baseline and the two-year follow-up period.
To determine whether long-term biologic therapy poses additional risk or provides any protective effect regarding the progression of liver disease.
Study Population:
Adult PsA patients aged 18 to 65 years, meeting standard classification criteria.
Biologic therapy group: ongoing anti-TNF or anti-IL-17 treatment for ≥2 years.
Control group: MTX therapy ≥2 years without biologic agents.
Methods:
Patient records from the rheumatology department will be reviewed retrospectively.
Liver ultrasonography, performed at baseline (or earliest available pre-biologic record) and at the two-year mark, will evaluate hepatic steatosis, if available in patient files.
Blood tests (AST, ALT, platelet count, total bilirubin, albumin, CRP) will be retrieved from clinical databases to calculate non-invasive liver fibrosis indices (e.g., FIB-4, APRI). Additional data on metabolic risk factors (BMI, diabetes, hypertension, dyslipidemia measured by total cholesterol, LDL, HDL, and triglyceride levels) will be extracted. Additionally, clinical information on enthesitis, dactylitis, and disease activity (assessed by DAPSA and/or PASI scores when available) will be recorded from patient files.
Statistical analysis will include group comparisons, correlation analyses, and multiple regression to adjust for confounding factors.
Significance:
Findings from this study will enhance understanding of whether TNF-alpha or IL-17 inhibitors elevate or mitigate the risk of liver disease progression relative to MTX therapy in PsA patients, providing a foundation for more tailored treatment decisions and long-term patient monitoring.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Outcome assessment at 24 months post-treatment initiation
The Fibrosis-4 (FIB-4) Index is a tool used for the noninvasive assessment of liver fibrosis. Comparison of liver fibrosis scores (FIB-4) calculated from AST, ALT, platelet counts, and age between Anti-TNF and Anti-IL17 treated Psoriatic Arthritis patients. There is no fixed minimum or maximum value; however, the following threshold values are commonly used in clinical interpretation:
<1.3: Low likelihood of advanced fibrosis 1.3-2.67: Indeterminate/intermediate risk >2.67: High likelihood of advanced fibrosis. Higher FIB-4 scores indicate the presence of more advanced liver fibrosis.
Time frame: Outcome assessment at 24 months post-treatment initiation
Determining the percentage of patients with elevated FIB-4 scores suggestive of liver fibrosis risk in each treatment group (Anti-TNF vs. Anti-IL17).Higher FIB-4 scores indicate the presence of more advanced liver fibrosis.
Contact information is provided by the study sponsor or research team.
Mehmet Serkan Kılıçoğlu, MD
CONTACT
Safa El Mardi Alaoui, MD
CONTACT
Bezmialem Vakif University
Other
Evaluation of Liver Fibrosis and Hepatic Steatosis Using FIB-4 Score and Ultrasonography in Psoriatic Arthritis Patients Treated With TNF or IL-17 Inhibitors: A Retrospective Controlled Study
Acronym: FIB-4 PsA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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