Evidence map›Paper›PMID 25834350›Full record

ArticleAnnals of dermatology2015

TNF, IL12B, and IFNG Gene Polymorphisms in Serbian Patients with Psoriasis.

Svetlana Popadic, Emina Savic, Milos Markovic, Zorica Ramic, Ljiljana Medenica, Vera Pravica, Zorica Spuran, Vladimir Trajkovic, Dusan Popadic

Abstract read
In one paragraph

Article in Annals of dermatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Association betweenHeliyon · 2023
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4 · The record

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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

9 authors.

Svetlana PopadicDepartment of Dermatovenereology, School of Medicine, University of Belgrade, Serbia. ; Clinic of Dermatovenereology, Clinical Center of Serbia, Serbia.
Emina SavicInstitute of Microbiology and Immunology, School of Medicine, University of Belgrade, Serbia.
Milos MarkovicInstitute of Microbiology and Immunology, School of Medicine, University of Belgrade, Serbia.
Zorica RamicInstitute of Microbiology and Immunology, School of Medicine, University of Belgrade, Serbia.
Ljiljana MedenicaDepartment of Dermatovenereology, School of Medicine, University of Belgrade, Serbia. ; Clinic of Dermatovenereology, Clinical Center of Serbia, Serbia.
Vera PravicaInstitute of Microbiology and Immunology, School of Medicine, University of Belgrade, Serbia.
Zorica SpuranBlood and Blood Component Collection Department, National Blood Transfusion Institute of Serbia, Belgrade, Serbia.
Vladimir TrajkovicInstitute of Microbiology and Immunology, School of Medicine, University of Belgrade, Serbia.
Dusan PopadicInstitute of Microbiology and Immunology, School of Medicine, University of Belgrade, Serbia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPsoriasis is a common chronic inflammatory skin disease with a strong genetic basis. Cytokines such as tumor necrosis factor alpha (TNF-α), interleukins (ILs) such are IL-12 and IL-23, and interferon gamma (IFN-γ) are released from various inflammatory and resident cells, and have been implicated in the initiation/maintenance of inflammation. Certain alleles of the aforementioned cytokines may be associated with disease susceptibility/severity.

objectiveTo investigate the association of three common functional gene polymorphisms, namely TNF -308 G/A (rs1800629), IL12B (encoding the p40 subunit of IL-12/23) +1188 A/C (rs3212227), and IFNG +874 T/A (rs2430561) with psoriasis development and severity in Serbian patients.

methodsWe genotyped 130 patients with psoriasis (26 of whom also had psoriatic arthritis) and 259 controls; rs1800629 and rs3212227, and rs2430561, by real-time PCR assay.

resultsThe TNF GG genotype was detected at a higher frequency in patients with psoriasis compared to control subjects (OR, 1.420; 95% CI, 0.870~2.403) without statistical significance (p=0.191). Lack of the TNF G allele was associated with lower psoriasis severity (p=0.007). The IL12B AC genotype was underrepresented in the patients with psoriatic arthritis compared to healthy subjects (OR, 0.308; 95% CI, 0.090~1.057; p=0.049). The distribution of the rs2430561 allele and genotype frequencies was similar between patients with psoriasis and controls.

conclusionOur study demonstrates an effect of the rs1800629 on psoriasis severity, and a marginal impact of the rs3212227 on susceptibility to psoriatic arthritis. Collectively, our results obtained in a Serbian cohort expand current knowledge regarding individual predisposition to psoriatic disease.

Indexed as

Allele frequenciesInterferon gammap40 IL-12/23PsoriasisReal-time PCRTumor necrosis factor-alpha

Identifiers

PMID25834350
PMCPMC4377400

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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.