Evidence map›Paper›PMID 41575605›Full record

ArticleDermatology and therapy2026

Evaluating Risankizumab's Long-Term Effects in Psoriasis Using Optical Coherence Tomography.

Henner Zirpel, Linh Ha-Wissel, Sarah Hobelsberger, Lena Pommerien, Stefan Beissert, Evelyn Gaffal, Ruth Bauer, Jenia Neumeister, Kristina Lohmann, Diamant Thaçi

Abstract read
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Article in Dermatology and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Henner Zirpel *Institute and Comprehensive Center for Inflammation Medicine, University of Lübeck, Lübeck, Germany.
Linh Ha-Wissel *Institute and Comprehensive Center for Inflammation Medicine, University of Lübeck, Lübeck, Germany.
Sarah HobelsbergerDepartment of Dermatology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Lena PommerienInstitute and Comprehensive Center for Inflammation Medicine, University of Lübeck, Lübeck, Germany.
Stefan BeissertDepartment of Dermatology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Evelyn GaffalDepartment of Dermatology, Allergology and Venerology, University Hospital Schleswig-Holstein Lübeck (UKSH), Lübeck, Germany.
Ruth BauerAbbVie Deutschland and Co. KG, Wiesbaden, Germany.
Jenia NeumeisterAbbVie Deutschland and Co. KG, Wiesbaden, Germany.
Kristina LohmannAbbVie Deutschland and Co. KG, Wiesbaden, Germany.
Diamant ThaçiInstitute and Comprehensive Center for Inflammation Medicine, University of Lübeck, Lübeck, Germany. Diamant.Thaci@uksh.de.ORCID http://orcid.org/0000-0001-8513-550X

Funding

Deutsche Forschungsgemeinschaft EXC2167/1
6 · The paper itself

Abstract

introductionPsoriasis is a chronic inflammatory disease associated with multiple systemic comorbidities and reduced quality of life. Risankizumab, an interleukin (IL)-23 inhibitor, has demonstrated efficacy in achieving rapid and sustained skin clearance in moderate-to-severe psoriasis. However, its impact on chronic subclinical inflammation is less understood. Conventional clinical assessments like Psoriasis Area and Severity Index (PASI), Investigator's Global Assessment (IGA), and Body Surface Area (BSA) focus on evaluating visible symptoms and are limited in capturing underlying disease activity. Optical coherence tomography (OCT), a non-invasive imaging modality, offers real-time assessment of structural and vascular changes, providing valuable insights beyond the skin surface.

methodsThis sub-analysis of a prospective, single-center exploratory study included 22 patients with moderate-to-severe psoriasis treated with risankizumab. Clinical assessments (PASI, IGA, BSA) were conducted at baseline and weeks 2, 4, 16, 28, 40, and 52. OCT imaging performed at baseline and weeks 4, 16, and 52 evaluated epidermal thickness and vascular parameters (e.g., vessel density and diameter) in lesional and perilesional skin.

resultsBy week 16, mean (95% confidence interval [CI]) PASI score decreased from 16.3 (11.6-21.1) at baseline to 3.5 (1.8-5.2), and BSA involvement from 24.7% (16.1-33.3) to 5.2% (1.9-8.4) (both p < 0.001). By week 52, 86.7%, 73.3%, and 40.0% of patients achieved PASI 75, 90, and 100, respectively, and 93.3% achieved IGA 0/1. OCT showed lesional reductions in epidermal thickness (- 37.4%), vessel density (- 26.6% Δ area under the curve [AUC]), and vessel diameter (- 59.5% ΔAUC) over the 52-week period. Notably, vascular changes also occurred in uninvolved perilesional skin.

conclusionRisankizumab improved both clinical and OCT parameters over 52 weeks, emphasizing the importance of long-term therapy with benefits extending beyond visible improvement. OCT emerged as a valuable tool for assessing deep (vascular) treatment response, thereby supporting a more comprehensive understanding of therapeutic outcomes in psoriasis.

Indexed as

Interleukin-23Optical coherence tomographyPsoriasisRisankizumab

Identifiers

PMID41575605
PMCPMC12936233

What Socratic holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.