Evidence map›Paper›PMID 32355229›Full record

ArticleGenes and immunity2020

IL12B and IL23R polymorphisms are associated with alopecia areata.

Pardis-Sadat Tabatabaei-Panah, Hamideh Moravvej, Sara Delpasand, Mona Jafari, Sanaz Sepehri, Reyhaneh Abgoon, Ralf J Ludwig, Reza Akbarzadeh

Abstract read
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In one paragraph

Article in Genes and immunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.8field-weighted citation impact, top 10% of its field
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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Evaluation ofAnnals of medicine and surgery (2012) · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. The Immunogenetics of Alopecia areata.Advances in experimental medicine and biology · 2022
    Article
  12. Review
  13. The Association Study ofFrontiers in neuroscience · 2020
    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

8 authors at 4 institutions in 2 countries.

Pardis-Sadat Tabatabaei-PanahBiology Department, East Tehran Branch, Islamic Azad University, Tehran, Iran.
Hamideh MoravvejSkin Research Centre, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Sara DelpasandBiology Department, East Tehran Branch, Islamic Azad University, Tehran, Iran.
Mona JafariBiology Department, East Tehran Branch, Islamic Azad University, Tehran, Iran.
Sanaz SepehriBiology Department, East Tehran Branch, Islamic Azad University, Tehran, Iran.
Reyhaneh AbgoonBiology Department, East Tehran Branch, Islamic Azad University, Tehran, Iran.
Ralf J LudwigLübeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany.
Reza AkbarzadehSkin Research Centre, Shahid Beheshti University of Medical Sciences, Tehran, Iran. akbarzadeh@anat.uni-luebeck.de.ORCID http://orcid.org/0000-0001-7668-702X
Islamic Azad University South Tehran Branch · IRShahid Beheshti University · IRShahid Beheshti University of Medical Sciences · IRUniversity of Lübeck · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alopecia areata is an autoimmune disease in which activation of autoreactive T cells and inflammatory immune signals target the hair follicles autoantigens. Although cytokines are involved in regulating autoimmune inflammation, the specific involvement of these molecules in the pathogenesis of alopecia areata has been remained unsettled. Here, a possible influence of IL12B, IL17A, and IL23R variations on susceptibility to alopecia areata in Iranian patients was investigated. Genotyping of IL12B (rs3212227), IL17A (rs2275913), and IL23R (rs10889677) variants were performed by extracting genomic DNA from patients and controls. Gene expression was analyzed by real-time RT-PCR. The frequency of IL12B and IL23R gene polymorphisms is significantly higher in the patients than controls, while no significant difference was found for IL17A. Stratification of the patients with respect to age at disease onset indicated that CC genotype of IL12B (rs3212227) and AA genotype of IL23R (rs10889677) gene polymorphisms are significantly associated with late-onset alopecia areata disease. In contrast to IL17A and IL23R, IL12B gene expression levels elevated in patients to that of controls, but genotypes had no effect on levels of gene expression. Overall, our data confirmed that the IL12B and IL23R polymorphisms are associated with the risk to develop alopecia areata in our population.

Indexed as

AdultAlopecia AreataFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHumansInterleukin-12 Subunit p40Interleukin-17IranMalePolymorphism, GeneticReceptors, InterleukinRisk FactorsIL12B protein, humanIL17A protein, humanIL23R protein, humanInterleukin-12 Subunit p40Interleukin-17Receptors, Interleukin

Identifiers

PMID32355229
OpenAlexW3022795263

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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.