Evidence map›Paper›PMID 23319986›Full record

ArticleArchives of medical science : AMS2012

Interleukin-17A and interleukin-23 in morphea.

Aleksandra Dańczak-Pazdrowska, Michał Kowalczyk, Beata Szramka-Pawlak, Justyna Gornowicz-Porowska, Aleksandra Szewczyk, Wojciech Silny, Anna Olewicz-Gawlik, Marta Molińska-Glura, Ryszard Zaba, Paweł Hrycaj

Open access · goldAbstract read
In one paragraph

Article in Archives of medical science : AMS, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

22 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Morphea: progress to date and the road ahead.Annals of translational medicine · 2021
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Morphea and Eosinophilic Fasciitis: An Update.American journal of clinical dermatology · 2017
    Review
  17. Effects of UVA1 Phototherapy on Expression of Human Endogenous Retroviral Sequence (HERV)-K10 gag in Morphea: A Preliminary Study.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  18. Significant reduction of peripheral blood interleukin-35 and CD4Central-European journal of immunology · 2017
    Article
  19. Article
  20. 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

10 authors at 1 institution in 1 country.

Aleksandra Dańczak-PazdrowskaDepartment of Dermatology, Poznan University of Medical Sciences, Poznan, Poland.
Michał Kowalczyk
Beata Szramka-Pawlak
Justyna Gornowicz-Porowska
Aleksandra Szewczyk
Wojciech Silny
Anna Olewicz-Gawlik
Marta Molińska-Glura
Ryszard Zaba
Paweł Hrycaj
Poznan University of Medical Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMorphea is a disease included in the group of scleroderma type autoimmune diseases. Interleukin (IL)-17A may play a role at every stage of its pathogenesis. The study aimed at evaluation of IL-17A and IL-23 (as the main cytokine which is supposed to stimulate and maintain synthesis of IL-17) in pathogenesis of morphea. MATERIAL AND

methodsThe studies were performed on 41 blood samples from patients with morphea. Skin was sampled from 29 patients. The evaluation included: (1) expression of IL-17A and IL-23 genes in peripheral blood mononuclear cells (PBMC) using real-time polymerase chain reaction (PCR), (2) plasma concentrations of IL-17A and IL-23 using ELISA, (3) expression of IL-17A and IL-23 genes in skin using real-time PCR.

resultsThe results of gene expression are expressed as median number of copies per million copies of GAPDH. Higher expression of IL-17A has been demonstrated in PBMC of morphea vs. control group (2630 and 1906 respectively; p = 0.004), accompanied by absence of significant differences in its plasma concentration (10 pg/ml in both groups) and by lowered expression in affected skin (9119 and 19113 respectively; p = 0.036). The results failed to demonstrate elevated IL-23 plasma concentration in morphea vs. control group (5 pg/ml and 6 pg/ml respectively; p = 0.335) or its increased expression in the skin (292 vs. 427; p = 0.383), although we noted its increased expression in PBMC (4419 vs. 808; p < 0.001).

conclusionsBASED ON THE OBSERVED CORRELATIONS WE SUGGEST THAT: (1) IL-17A does not represent a factor which promotes tissue injury in morphea, (2) IL-23 may playa role in pathogenesis of morphea.

Indexed as

autoimmune diseasesinterleukin 17interleukin 23morpheascleroderma

Identifiers

PMID23319986
PMCPMC3542501
OpenAlexW2117407737

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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.