Evidence map›Paper›PMID 31891686›Full record

ArticleThe Journal of allergy and clinical immunology2020

Progression of acute-to-chronic atopic dermatitis is associated with quantitative rather than qualitative changes in cytokine responses.

Lam C Tsoi, Elke Rodriguez, Dora Stölzl, Ulrike Wehkamp, Jingru Sun, Sascha Gerdes, Mrinal K Sarkar, Matthias Hübenthal, Chang Zeng, Ranjitha Uppala and 13 more

Erratum issued Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT05140239 (Effects of Abrocitinib Treatment of Moderate to Severe Atopic Dermatitis on Skin Barrier Function), which is not on this map. Cited by 115 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed, 3 pooled it
12.4field-weighted citation impact, top 1% 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.

NCT05140239 completednot on this mapstarted 2022, after this paper: background citation

Effects of Abrocitinib Treatment of Moderate to Severe Atopic Dermatitis on Skin Barrier Function

TypeobservationalSponsorProf. Dr. Stephan WeidingerRan2022 to 2024Enrolled20ConditionsAtopic DermatitisArmsNo Intervention
3 · Its place in the literature

Who cites it

115 citing papers in PubMed, 3 syntheses or guidelines pooled it, 199 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Observational
  6. Review
  7. Article
  8. Article
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  10. Article
  11. Review
  12. Article
  13. Atopic dermatitis.Nature reviews. Disease primers · 2026
    Review
  14. Article
  15. Sexual Dimorphism in Allergic and Mast Cell-Associated Diseases.Clinical reviews in allergy & immunology · 2026
    Review
  16. Article
  17. Dysbiosis in the Pathogenesis of Atopic Dermatitis.The Journal of dermatology · 2026
    Review
  18. Article
  19. Article
  20. Article

55 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 5 institutions in 3 countries.

Lam C TsoiDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Mich; Department of Computational Medicine & Bioinformatics, University of Michigan Medical School, Ann Arbor, Mich; Department of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, Mich.
Elke RodriguezDepartment of Dermatology, Venereology and Allergy, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Dora StölzlDepartment of Dermatology, Venereology and Allergy, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Ulrike WehkampDepartment of Dermatology, Venereology and Allergy, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Jingru SunDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Mich.
Sascha GerdesDepartment of Dermatology, Venereology and Allergy, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Mrinal K SarkarDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Mich.
Matthias HübenthalDepartment of Dermatology, Venereology and Allergy, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Chang ZengDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Mich.
Ranjitha UppalaDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Mich; Immunology Graduate Program, University of Michigan Medical School, Ann Arbor, Mich.
Xianying XingDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Mich.
Frederieke ThielkingDepartment of Dermatology, Venereology and Allergy, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Allison C BilliDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Mich.
William R SwindellHeritage College of Osteopathic Medicine, Ohio University, Athens, Ohio; Jewish Hospital, Department of Internal Medicine, Cincinnati, Ohio.
Alanna SheflerDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Mich.
Jiahan ChenDepartment of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, Mich.
Matthew T PatrickDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Mich.
Paul W HarmsDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Mich; Department of Pathology, University of Michigan Medical School, Ann Arbor, Mich.
J Michelle KahlenbergDivision of Rheumatology, Internal Medicine, University of Michigan Medical School, Ann Arbor, Mich.
Bethany E Perez WhiteDepartment of Dermatology, Northwestern University, Chicago, Ill.
Emanual MaverakisDepartment of Dermatology, School of Medicine, UC-Davis Medical Center, Sacramento, Calif.
Johann E GudjonssonDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Mich. Electronic address: johanng@med.umich.edu.
Stephan WeidingerDepartment of Dermatology, Venereology and Allergy, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
University of Michigan · USUniversity Hospital Schleswig-Holstein · DENorthwestern University · PHOhio University · USUniversity of California Davis Medical Center · US

Funding

University of Michigan Skin Biology and Diseases Resource-based CenterP30AR075043 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ANDRZEJ A. DLUGOSZ · 2019 to 2026
$6.6M
TRAINING PROGRAM IN CELL AND MOLECULAR DERMATOLOGYT32AR007197 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JAMES TILFORD ELDER, Sunny Y Wong · 1986 to 2026
$4.2M
Role of the sex biased transcription factor VGLL3 in promoting autoimmune responses in SLER01AI130025 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Johann Eli Gudjonsson · 2017 to 2026
$3.9M
Role of IL-13 and the IL-13 Associated rs20541 Risk Variant in the Pathogenesis of PsoriasisR01AR069071 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GUDJONSSON, JOHANN ELI · 2015 to 2019
$2.1M
Role of the Psoriasis Associated IL23R Risk Variants on Th17 Biology and FunctionK08AR060802 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GUDJONSSON, JOHANN ELI · 2011 to 2015
$636k
Integrative Biology Approach to Identify and Characterize Roles of lncRNAs Associated with Psoriasis PathologyK01AR072129 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TSOI, LAM CHEUNG · 2017 to 2021
$500k
Breaking down barriers: defining the role of EphA2 in building epidermal tight junctions in atopic dermatitisK01AR072773 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PEREZ WHITE, BETHANY E · 2018 to 2021
$333k
NIAID NIH HHS R01 AI130025NIAMS NIH HHS K01 AR072129NIAMS NIH HHS K01 AR072773NIAMS NIH HHS K08 AR060802NIAMS NIH HHS L40 AR076139NIAMS NIH HHS P30 AR075043NIAMS NIH HHS R01 AR069071NIAMS NIH HHS T32 AR007197
6 · The paper itself

Abstract

backgroundAlthough multiple studies have assessed molecular changes in chronic atopic dermatitis (AD) lesions, little is known about the transition from acute to chronic disease stages, and the factors and mechanisms that shape chronic inflammatory activity.

objectivesWe sought to assess the global transcriptome changes that characterize the progression from acute to chronic stages of AD.

methodsWe analyzed transcriptome changes in paired nonlesional skin, acute and chronic AD lesions from 11 patients and 38 healthy controls by RNA-sequencing, and conducted in vivo and histological assays to evaluate findings.

resultsOur data demonstrate that approximately 74% of the genes dysregulated in acute lesions remain or are further dysregulated in chronic lesions, whereas only 34% of the genes dysregulated in chronic lesions are altered already in the acute stage. Nonlesional AD skin exhibited enrichment of TNF, T

conclusionsOur results show that the changes accompanying the transition from nonlesional to acute to chronic inflammation in AD are quantitative rather than qualitative, with chronic AD having heightened T

Indexed as

Acute DiseaseChronic DiseaseCytokinesDermatitis, AtopicFemaleHumansMaleSequence Analysis, RNATh17 CellsTh1 CellsTh2 CellsTranscriptomeCytokinesacute ADAtopic dermatitischronic ADnonlesionalRNA-sequencing

Identifiers

PMID31891686
PMCPMC7214216
OpenAlexW2998661193

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.