Evidence map›Paper›PMID 33975024›Full record

ArticleAnnals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology2021

Immune and barrier characterization of atopic dermatitis skin phenotype in Tanzanian patients.

Claudia C V Lang, Yael Renert-Yuval, Ester Del Duca, Ana B Pavel, Jianni Wu, Ning Zhang, Celina Dubin, Ashley Obi, Mashkura Chowdhoury, Madeline Kim and 8 more

Open access · greenAbstract read
In one paragraph

Article in Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Observational
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  8. The mRNA expression and secretion of granzyme B are up-regulated via the histamine H2 receptor in human CD4Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Article
  9. Article
  10. Review
  11. CCL13 and human diseases.Frontiers in immunology · 2023
    Review
  12. Biomarkers in atopic dermatitis and psoriasis-a Delphi-based guide through the jungle?Journal of the European Academy of Dermatology and Venereology : JEADV · 2022
    Article
  13. Review
  14. Article
  15. Review
  16. 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

18 authors at 5 institutions in 4 countries.

Claudia C V LangLaboratory of Inflammatory Skin Diseases, Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York; Department of Dermatology, University Hospital Zürich, Zürich, Switzerland.
Yael Renert-YuvalLaboratory of Inflammatory Skin Diseases, Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York; Laboratory for Investigative Dermatology, The Rockefeller University, New York, New York.
Ester Del DucaLaboratory of Inflammatory Skin Diseases, Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York; Department of Dermatology, University of Magna Graecia, Catanzaro, Italy.
Ana B PavelLaboratory of Inflammatory Skin Diseases, Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York; Department of Biomedical Engineering, University of Mississippi, Oxford, Mississippi.
Jianni WuLaboratory of Inflammatory Skin Diseases, Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York.
Ning ZhangLaboratory of Inflammatory Skin Diseases, Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York.
Celina DubinLaboratory of Inflammatory Skin Diseases, Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York.
Ashley ObiLaboratory of Inflammatory Skin Diseases, Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York.
Mashkura ChowdhouryLaboratory of Inflammatory Skin Diseases, Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York.
Madeline KimLaboratory of Inflammatory Skin Diseases, Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York.
Yeriel D EstradaLaboratory of Inflammatory Skin Diseases, Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York.
James G KruegerLaboratory for Investigative Dermatology, The Rockefeller University, New York, New York.
Hashim KaderbhaiDepartment of Dermatology, M.P. Shah Hospital, Nairobi, Kenya; Department of Dermatology, Regional Dermatology Training Center, Moshi, Tanzania.
George SemangoDepartment of Dermatology, Regional Dermatology Training Center, Moshi, Tanzania.
Peter Schmid-GrendelmeierDepartment of Dermatology, University Hospital Zürich, Zürich, Switzerland.
Marie-Charlotte BrüggenDepartment of Dermatology, University Hospital Zürich, Zürich, Switzerland; Hochgebirgsklinik Davos, Davos, Switzerland.
John E MasengaDepartment of Dermatology, Regional Dermatology Training Center, Moshi, Tanzania.
Emma Guttman-YasskyLaboratory of Inflammatory Skin Diseases, Department of Dermatology, Icahn School of Medicine at Mount Sinai, New York, New York. Electronic address: Emma.Guttman@mountsinai.org.
Icahn School of Medicine at Mount Sinai · USUniversity Hospital of Zurich · CHRockefeller University · USMagna Graecia University · ITNairobi Hospital · KE

Funding

Developing, Demonstrating, and Disseminating Innovative Programs to Achieve Translational SuccessUL1TR001866 · NCATS · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY, KRUEGER, JAMES G · 2016 to 2025
$40.6M
NCATS NIH HHS UL1 TR001866
6 · The paper itself

Abstract

backgroundAtopic dermatitis (AD) is a common disease, with particularly high prevalence found in Africa. It is increasingly recognized that patients with AD of different ethnic backgrounds have unique molecular signatures in the skin, potentially accounting for treatment response variations. Nevertheless, the skin profile of patients with AD from Africa is unknown, hindering development of new treatments targeted to this patient population.

objectiveTo characterize the skin profile of patients with AD from Africa.

methodsGene expression studies, including RNA sequencing (using threshold of fold change of >2 and false discovery rate of <0.05) and real-time polymerase chain reaction, were performed on skin biopsies of Tanzanian patients with moderate-to-severe AD and controls.

resultsTanzanian AD skin presented robust up-regulations of multiple key mediators of both T helper 2 (T

conclusionThe skin phenotype of Tanzanian patients with AD is consistent with that of African Americans, exhibiting dominant T

Indexed as

AdultBlack or African AmericanBlack PeopleCytokinesDermatitis, AtopicFemaleFilaggrin ProteinsGene ExpressionHumansLipid MetabolismMalePhenotypeSeverity of Illness IndexSkinTanzaniaCytokinesFilaggrin ProteinsFLG protein, human

Identifiers

PMID33975024
PMCPMC11344219
OpenAlexW3160147150

What OpenQuestion holds

Textmetadata
LicenceTDM
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.