Evidence map›Paper›PMID 42726432›Full record

ArticleClinical rheumatology2026

Paradoxical psoriasis in axial spondyloarthritis and rheumatoid arthritis treated with b/tsDMARDs: a retrospective cohort study.

Halil Harman, Tuğba İşlek, Deniz Doğan, Mehmet Ali Balcı

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Article in Clinical rheumatology, 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Halil HarmanRheumatology Division, Physical Medicine and Rehabilitation Education and Research Hospital, University of Health Sciences, Istanbul, Türkiye. drhharman@yahoo.com.ORCID http://orcid.org/0000-0003-4178-8730
Tuğba İşlekRheumatology Division, Physical Medicine and Rehabilitation Education and Research Hospital, University of Health Sciences, Istanbul, Türkiye.ORCID http://orcid.org/0000-0003-0566-1169
Deniz DoğanRheumatology Division, Physical Medicine and Rehabilitation Education and Research Hospital, University of Health Sciences, Istanbul, Türkiye.ORCID http://orcid.org/0000-0002-0087-2701
Mehmet Ali BalcıRheumatology Division, Physical Medicine and Rehabilitation Education and Research Hospital, University of Health Sciences, Istanbul, Türkiye.ORCID http://orcid.org/0000-0003-0597-7788

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

INTRODUCTION/

objectivesTo determine the incidence of paradoxical psoriasis (PP) across multiple b/tsDMARD classes, identify independent risk factors, and characterise the clinical features and treatment outcomes of PP in axial spondyloarthritis (axSpA) and rheumatoid arthritis (RA).

methodsSingle-centre retrospective cohort study of 1588 adult patients with axSpA or RA receiving at least one b/tsDMARD between January 2019 and December 2024. PP was defined as de novo psoriasiform skin lesions confirmed by dermatological evaluation. Incidence rates were calculated per 100 person-years. Risk factors were assessed by multivariable Firth penalised logistic regression and Kaplan-Meier analysis.

resultsPP developed in 32 patients (2.0%) over 2795.7 person-years (incidence rate 1.14/100 PY; 95% CI 0.78-1.62). Thirty cases (93.8%) occurred with TNF inhibitors. No PP was observed with JAK inhibitors, rituximab, or tocilizumab. The predominant phenotype was palmoplantar pustular psoriasis (65.6%); median time to onset was 12.0 months (IQR 5.2-25.2). Ever-smoking was the sole independent predictor of PP (adjusted OR 2.15; p = 0.043); TNF inhibitor use and family history showed borderline associations. Kaplan-Meier analysis confirmed higher cumulative PP incidence in ever-smokers (log-rank p = 0.031). The causative b/tsDMARD was discontinued in 27 patients (84.4%); complete remission was achieved in 15 (55.6%).

conclusionsPP occurs predominantly with TNF inhibitor therapy and is independently predicted by ever-smoking status. Palmoplantar pustular psoriasis is the predominant phenotype. Drug discontinuation leads to complete remission in the majority of patients, and non-TNF b/tsDMARDs may be considered as alternatives following PP development. Key Points • Paradoxical psoriasis occurs in 2% of axSpA and RA patients on b/tsDMARDs, almost exclusively with TNF inhibitors. • Ever-smoking is the sole independent predictor; smokers initiating TNF inhibitors warrant proactive skin monitoring. • Drug discontinuation achieves complete remission in most patients; non-TNF b/tsDMARDs are effective alternatives.

Indexed as

Axial spondyloarthritisBiological DMARDs, smokingIncidencePalmoplantar pustulosisParadoxical psoriasisRheumatoid arthritisTNF inhibitors

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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.