Evidence map›Paper›PMID 40109802›Full record

ReviewCureus2025

Therapeutic Advancements in the Management of Psoriasis: A Clinical Overview and Update.

Sarah F Qasem, Hasan Ashkanani, Ali Ali

Abstract readReview
In one paragraph

Review in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
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

3 authors.

Sarah F QasemDermatology, Amiri Hospital, Ministry of Health, Kuwait City, KWT.
Hasan AshkananiDermatology, Amiri Hospital, Ministry of Health, Kuwait City, KWT.
Ali AliInternal Medicine, Mubarak Al-Kabeer Hospital, Jabriya, KWT.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Psoriasis is an autoimmune chronic inflammatory skin condition with a strong genetic predisposition. Pathogenesis of psoriasis is complex and multifactorial; it is known that genetic, immunological, and environmental factors play significant roles in its development. Treatment options vary and include topical therapy (e.g., corticosteroids, vitamin D analogs, and calcineurin inhibitors), phototherapy (e.g., narrowband ultraviolet radiation (NB-UVB)), and systemic therapy (e.g., methotrexate and retinoids). Several new treatments have emerged in recent years, including biological treatments. Biologics approved by the United States Food and Drug Administration (FDA) for the treatment of psoriasis include inhibitors of tumor necrosis factor (TNF)-α. Other FDA-approved biologics for the treatment of psoriasis target cytokines, such as the p40 subunit of interleukin (IL)-12 and IL-23, IL-17, as well as the p19 subunit of IL-23. Additionally, the Janus kinase (JAK) inhibitor deucravacitinib is also FDA-approved for the treatment of moderate-to-severe psoriasis. Other promising treatment modalities are consistently undergoing trials. Further therapeutic details, including regimens, side effects, indications, contraindications, and FDA approval dates, are discussed comprehensively in this article. For the purpose of this review, the literature was thoroughly searched for publications discussing psoriasis therapy. This review aims to provide a comprehensive overview and update on the management of psoriasis.

Indexed as

biologicsmanagementnailspsoriasisskin

Identifiers

PMID40109802
PMCPMC11920851

What OpenQuestion holds

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Registered trials

None linked

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.