Evidence map›Paper›PMID 41893339›Full record

ArticleMetabolites2026

Serum Semaphorin Alterations in Psoriasis: Links to Metabolic Status Rather than Disease Severity.

Anna Baran, Anna Stepaniuk, Justyna Magdalena Hermanowicz, Beata Sieklucka, Krystyna Pawlak, Dariusz Pawlak, Iwona Flisiak

Abstract read
In one paragraph

Article in Metabolites, 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

The trial behind it

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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

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

7 authors.

Anna BaranDepartment of Dermatology and Venereology, Medical University of Bialystok, Zurawia 14 St., 15-540 Bialystok, Poland.ORCID 0000-0002-8018-9960
Anna StepaniukDepartment of Dermatology and Venereology, Medical University of Bialystok, Zurawia 14 St., 15-540 Bialystok, Poland.ORCID 0000-0003-1414-4569
Justyna Magdalena HermanowiczDepartment of Pharmacodynamics, Medical University of Bialystok, Mickiewicza 2C St., 15-540 Bialystok, Poland.ORCID 0000-0002-3985-4244
Beata SiekluckaDepartment of Monitored Pharmacotherapy, Medical University of Bialystok, Mickiewicza 2C St., 15-222 Bialystok, Poland.
Krystyna PawlakDepartment of Monitored Pharmacotherapy, Medical University of Bialystok, Mickiewicza 2C St., 15-222 Bialystok, Poland.ORCID 0000-0003-2254-7982
Dariusz PawlakDepartment of Pharmacodynamics, Medical University of Bialystok, Mickiewicza 2C St., 15-540 Bialystok, Poland.ORCID 0000-0002-3751-0608
Iwona FlisiakDepartment of Dermatology and Venereology, Medical University of Bialystok, Zurawia 14 St., 15-540 Bialystok, Poland.ORCID 0000-0002-5923-910X

Funding

Medical University of Bialystok APK.002.358.2022
6 · The paper itself

Abstract

introductionPsoriasis is an autoimmune systemic disease of not entirely understood pathogenesis. It remains a significant therapeutic challenge and, due to its various comorbidities, has a remarkable detrimental effect on patients' wellbeing. Semaphorins (Sema) are a group of transmembrane, cell surface-attached and secretory proteins that might play an important role in psoriasis due to their presence on keratinocytes and the ability to stimulate the proinflammatory cytokine production.

aimsThe study aimed to assess the concentration of Sema3A, Sema3E, Sema4A, Sema4D and Sema7A in serum samples of psoriatic patients and explore the correlation with disease activity and clinical and metabolic status. MATERIALS AND

methodsThe study involved 60 patients with plaque psoriasis and 30 healthy volunteers matched for gender, age, and BMI.

resultsThe mean serum Sema3A, Sema3E and Sema4D levels were significantly higher in patients with psoriasis than controls (

conclusionsPsoriatic patients exhibited distinct alterations in circulating semaphorins, with significantly increased serum Sema3A, Sema3E and Sema4D, and reduced Sema4A and Sema7A compared with healthy subjects. Selected semaphorins demonstrated associations with metabolic parameters and patient characteristics, although none can serve as marker of disease severity. The findings indicate that semaphorins may reflect psoriasis-related systemic disturbances, but further studies are required to explore their potential with disease-associated metabolic or clinical profiles.

Indexed as

atherosclerosiscomorbiditiesmetabolic syndromepsoriasisSema3ASema3ESema4ASema4DSema7Asemaphorinssystemic therapy

Identifiers

PMID41893339
PMCPMC13028390

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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.