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Psoriasis is associated with comorbidities like metabolic syndrome and nonalcoholic fatty liver disease, increasing the risk of liver fibrosis. This study evaluated the long-term effects of guselkumab on liver fibrosis in 154 psoriasis patients using the Fibrosis-4 (FIB-4) index, a noninvasive marker of fibrosis, over 3 years. Patients were stratified by baseline FIB-4 (≥ 1.3 or < 1.3) and age (35-65 years). Mean FIB-4 values remained stable across all subgroups, with no significant changes observed. High-risk patients (FIB-4 ≥ 1.3) showed minor, nonsignificant fluctuations, while low-risk patients (FIB-4 < 1.3) exhibited a mild, age-related upward trend. Disease duration emerged as a key factor influencing FIB-4, highlighting the importance of early treatment. These findings suggest guselkumab does not contribute to liver fibrosis progression in psoriasis patients. Further research with advanced methods like imaging or biopsy is needed to confirm the long-term hepatic safety of IL-23 inhibitors like guselkumab.
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http://dx.doi.org/10.1111/1346-8138.17752 | DOI Listing |
Australas J Dermatol
September 2025
Department of Dermatology, Consorcio Hospital General Universitario, Valencia, Spain.
Managing moderate-to-severe psoriasis in patients with current or past malignancy remains a therapeutic challenge. We conducted a multicentre, retrospective real-world study to assess the safety and effectiveness of guselkumab in this complex population. Thirty patients were included, of whom 11 had active cancer at the time of guselkumab initiation.
View Article and Find Full Text PDFChin Med J (Engl)
September 2025
Department of Dermatology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310006, China.
Background: Guselkumab is effective in treating moderate-to-severe plaque psoriasis; however, data from randomized controlled trials in the Chinese population are limited. This study evaluated and verified the efficacy and safety profile of guselkumab in Chinese patients with moderate-to-severe plaque psoriasis.
Methods: This was a randomized, double-blind, placebo-controlled, phase 4 study.
Front Med (Lausanne)
August 2025
Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Background: Psoriasis is associated with increased cardiovascular risk, possibly mediated by inflammation-induced hemostatic dysregulation and hypercoagulability. However, these changes are often difficult to detect with conventional markers.
Objectives: To assess hypercoagulability in patients with psoriasis using the Overall Hemostatic Potential (OHP) test, a global integrative test for coagulation and fibrinolysis.
Br J Dermatol
August 2025
Department of Dermatology, Yale University School of Medicine, New Haven, CT, USA.
Background: Patients with psoriasis affecting a low percentage of their body surface area (BSA) are underrepresented in clinical studies and may face substantial disease burden if high-impact sites are affected.
Objectives: SPECTREM is a Phase 3b, randomized, placebo-controlled study evaluating guselkumab efficacy and safety in participants with low BSA (2%-15%), moderate (Investigator's Global Assessment [IGA]=3) plaque psoriasis involving ≥1 high-impact site (scalp, face, genitals, intertriginous areas).
Methods: Eligible participants were randomized 2:1 to receive guselkumab 100 mg or placebo at Week 0 and Week 4, then every 8 weeks.