Evidence map›Paper›PMID 41035834›Full record

ArticleSkin health and disease2025

Effective management of psoriasis and psoriatic arthritis in a patient with systemic lupus erythematosus using deucravacitinib, mycophenolate mofetil and hydroxychloroquine.

Caroline Gewiss, Oliver M Steinmetz, Lukas Roth, Matthias Augustin, Nesrine Ben-Anaya

Abstract readCase Reports
In one paragraph

Article in Skin health and disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
4 · The record

Corrections and comments

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

5 authors.

Caroline GewissInstitute for Health Services Research in Dermatology and Nursing Professions (IVDP), University Medical Centre Hamburg Eppendorf (UKE), Hamburg, Germany.ORCID https://orcid.org/0000-0002-7803-9699
Oliver M SteinmetzIII. Department of Internal Medicine, University Medical Centre Hamburg Eppendorf (UKE), Hamburg, Germany.
Lukas RothImmunology Center Hamburg, Rheumatology Clinic, Specialist Medical Center Struenseehaus, Hamburg, Germany.
Matthias AugustinInstitute for Health Services Research in Dermatology and Nursing Professions (IVDP), University Medical Centre Hamburg Eppendorf (UKE), Hamburg, Germany.ORCID https://orcid.org/0000-0002-4026-8728
Nesrine Ben-AnayaInstitute for Health Services Research in Dermatology and Nursing Professions (IVDP), University Medical Centre Hamburg Eppendorf (UKE), Hamburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the case of a 32-year-old woman with severe psoriasis, psoriatic arthritis (PsA) and systemic lupus erythematosus (SLE), including lupus nephritis. Despite effective control of her SLE and PsA with hydroxychloroquine, mycophenolate mofetil (MMF) and belimumab, her psoriatic skin manifestations worsened over time. The differing therapeutic responses of these two autoimmune diseases are rooted in their distinct pathogenesis: SLE treatments target B cells, autoantibodies and interferon signalling, while psoriasis requires therapies inhibiting the interleukin (IL)-23/IL-17 axis or tumour necrosis factor-α to address cutaneous inflammation and keratinocyte proliferation. There is limited evidence suggesting that MMF may suppress joint inflammation in PsA, but it does not effectively control psoriatic skin manifestations. Given the negative impact on her quality of life, deucravacitinib, a selective tyrosine kinase 2 inhibitor, was initiated at the approved dose of 6 mg daily. To avoid overimmunosuppression, belimumab was halted. Within 3 months, the patient's Psoriasis Area and Severity Index (PASI) improved from 23 to 1.2, body surface area from 70% to 2% and Dermatology Life Quality Index (DLQI) from 15 to 2, with no joint pain and no SLE flare-ups. After 6 and 9 months, her skin manifestations remained in remission (PASI 1.2 and PASI 0, respectively), DLQI was 0 and joint symptoms remained fully controlled. No significant side effects or infections were observed. These findings suggest deucravacitinib may offer an effective treatment alternative for patients with overlapping autoimmune diseases, without compromising SLE control or increasing infection risk.

Identifiers

PMID41035834
PMCPMC12480730

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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 OpenQuestion graph.