Effects of IL17/23 Inhibitors on Markers of Subclinical Atherosclerosis in Patients With Psoriasis
- Sponsor
- National and Kapodistrian University of Athens
- Study ID
- NCT07169682
- Status
- Completed
Conditions
- Atherosclerosis
- Cardiovascular Disease
- Psoriasis
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- interleukin 17 inhibitor — DRUG52 weeks
- interleukin-23 inhibitor — DRUG52 weeks
- conventional systemic agent or apremilast — DRUG52 weeks
Study Details
Data on the antiatherogenic effect of IL23 inhibitors are sparse. This study aimed to assess the impact of one-year treatment with an IL17 or IL23 inhibitor on arterial stiffness in patients with moderate-to-severe psoriasis. This observational cohort study included patients with moderate-to-severe psoriasis treated with either an IL17 inhibitor or an IL23 inhibitor or a conventional systemic agent/apremilast (control group) for 52 weeks. The primary outcome was the evaluation of changes in carotid-femoral pulse wave velocity (PWV) and augmentation index normalized to 75 beats/min (AIx75) after 24 and 52 weeks. Secondary outcomes were the comparison of change in PWV and AIx75 between the study groups and the assessment of psoriasis disease severity scores and in ankle-brachial index (ABI).
Key Dates
- First listed
- Sep 12, 2025
- Start date
- Sep 1, 2021
- Status verified
- Sep 2025
- Primary completion
- Sep 30, 2024
- Completion
- Sep 30, 2024
Study Design
- Enrollment
- 66 participants (actual)
Arms
- Arm: Group 1IL17 inhibitor
- Arm: Group 2IL23 inhibitor
- Arm: Group 3conventional systemic agent or apremilast
Primary Outcome Measure
change of pulse wave velocity (PWV) from baseline to week 24 and 52 [ Time Frame: from enrollment to the end of treatment at week 52 ]
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