Evidence map›Paper›PMID 40565595›Full record

ArticleGenes2025

Several Proinflammatory Genes' Variability and Phenotypes of Atopic Dermatitis in Czech Adult AD Patients.

Vladimír Vašků, Anna Vašků

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Article in Genes, 2025. 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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Vladimír Vašků1st Department of Dermatology, St. Ann's Faculty Hospital, Faculty of Medicine, Masaryk University, 60200 Brno, Czech Republic.
Anna VaškůDepartment of Pathophysiology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.ORCID 0000-0002-9956-5823

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe etiopathogenesis of atopic dermatitis is complicated, and it includes aspects such as dysfunction of the skin barrier, changes in immune responses, IgE-mediated hypersensitivity, and many characteristics of the environment. Regarding skin barrier dysfunction, a number of genetic changes have been described. This genetic predisposition could be related to the phenotypes of atopic dermatitis.

aimIn this study, several polymorphisms in five proinflammatory genes were associated with certain phenotypes of AD patients (genotype-phenotype study).

methodsIn total, 89 unrelated AD Czech (Caucasian) patients were genotyped regarding five proinflammatory gene polymorphisms (angiotensinogen AGT M235T, AGT-6 G/A, TNF-α-238 G/A, TNF-β Fok1, IL-6-174 C/G and IL-6-596 G/A). Genotyping was performed using PCR and restriction analysis. For phenotypes, patients' sex, age and personal and family history of atopy, aero- and food allergies and other complex diseases were evaluated.

resultsA significant association with transepidermal water loss (TEWL) measured on the forearm was found with the AGT M235T polymorphism (

conclusionsOur results in the field of cytokine signaling in the immune system in patients with atopic dermatitis are in agreement with those of GWASs. We suggest that cost-effective and simple PCR tests may be the best approach for the rapid and optimal collection of valid genetic information in clinical practice.

Indexed as

Dermatitis, AtopicAdultCzech RepublicFemaleGenetic Predisposition to DiseaseGenotypeHumansInterleukin-6MaleMiddle AgedPhenotypePolymorphism, Single NucleotideTumor Necrosis Factor-alphaYoung AdultInterleukin-6Tumor Necrosis Factor-alphaatopic dermatitisfamily historygeneticsmarkerphenotype

Identifiers

PMID40565595
PMCPMC12192341

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