Effects of IL17/23 Inhibitors on Markers of Subclinical Atherosclerosis in Patients With Psoriasis

National and Kapodistrian University of Athens

Status

Completed

Conditions

Psoriasis

Atherosclerosis

Cardiovascular Disease

Treatments

Drug: conventional systemic agent or apremilast

Drug: interleukin 17 inhibitor

Drug: interleukin-23 inhibitor

Study type

Observational

Funder types

Other

Identifiers

NCT07169682

3610/20-05-2021

Details and patient eligibility

About

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).

Enrollment

66 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Moderate-to-severe psoriasis (Psoriasis Area Severity Index (PASI) score > 10 or Body Surface Area (BSA) >10 or Dermatology Life Quality Index (DLQI) >10)
Indication for treatment with an IL17 or an IL23 inhibitor based on disease characteristics and comorbidities

Exclusion criteria

Prior treatment with an IL17 or an IL23 inhibitor
Prior therapy with an TNFa-inhibitor for up to 3 months before entering the study
Chronic or severe acute infections, malignancy
Pregnancy or lactation