Evidence map›Paper›PMID 36773824›Full record

Observational studyJournal of the American Academy of Dermatology2023

Proteomic characterization of atopic dermatitis blood from infancy to adulthood.

Ester Del Duca, Yael Renert-Yuval, Ana B Pavel, Daniela Mikhaylov, Jianni Wu, Rachel Lefferdink, Milie Fang, Anjani Sheth, Alli Blumstein, Paola Facheris and 5 more

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in Journal of the American Academy of Dermatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
8.8field-weighted citation impact, top 2% 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

14 citing papers in PubMed, 31 citations in OpenAlex.

  1. Age-related changes of FCGR3AEBioMedicine · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. MicroRNA-939 amplifiesFrontiers in immunology · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Atopic Dermatitis in the Elderly Population.Acta dermato-venereologica · 2023
    Article
  14. Review
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

15 authors at 5 institutions in 2 countries.

Ester Del DucaDepartment of Dermatology and Laboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York; Department of Dermatology, University of Magna Graecia, Catanzaro, Italy.
Yael Renert-YuvalLaboratory for Investigative Dermatology, the Rockefeller University, New York, New York.
Ana B PavelDepartment of Dermatology and Laboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York; Department of Biomedical Engineering, University of Mississippi, University, Mississippi.
Daniela MikhaylovDepartment of Dermatology and Laboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York.
Jianni WuDepartment of Dermatology and Laboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York.
Rachel LefferdinkDepartment of Dermatology and Paediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Milie FangDepartment of Dermatology and Paediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Anjani ShethDepartment of Dermatology and Paediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Alli BlumsteinDepartment of Dermatology and Paediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
Paola FacherisDepartment of Dermatology and Laboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York; Department of Biomedical Science, Humanitas University, Pieve Emanuele, Italy.
Yeriel D EstradaDepartment of Dermatology and Laboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York.
Stephanie M RangelDepartment of Dermatology and Paediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois.
James G KruegerLaboratory for Investigative Dermatology, the Rockefeller University, New York, New York.
Amy S PallerDepartment of Dermatology and Paediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois. Electronic address: apaller@northwestern.edu.
Emma Guttman-YasskyDepartment of Dermatology and Laboratory of Inflammatory Skin Diseases, Icahn School of Medicine at Mount Sinai, New York; Laboratory for Investigative Dermatology, the Rockefeller University, New York, New York. Electronic address: emma.guttman@mountsinai.org.
Northwestern University · USIcahn School of Medicine at Mount Sinai · USRockefeller University · USHumanitas University · ITUniversity of Mississippi · US

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
Northwestern University Skin Disease Research Center Resource-based CenterP30AR075049 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Irina Budunova · 2019 to 2026
$6.6M
NCATS NIH HHS UL1 TR001866NIAMS NIH HHS P30 AR075049
6 · The paper itself

Abstract

backgroundPatients with atopic dermatitis (AD) have systemic biomarker dysregulation that differs by age group; however, the proteomic characteristics of these age-based changes are unknown.

objectiveTo profile blood proteins of patients with AD across different age groups versus age-appropriate controls.

methodsUsing the Olink high-throughput proteomic platform, we profiled 375 serum proteins of 20 infants (age, 0-5 years), 39 children (age, 6-11 years), 21 adolescents (age, 12-17 years), and 20 adults (age, ≥18 years) with moderate-to-severe AD and 83 age-appropriate controls.

resultsEach group presented a distinct systemic proteomic signature. Th2-related proteins were increased in infant AD and further intensified with age through adolescence and adulthood (interleukin 4/CCL13/CCL17). In contrast, Th1 axis down-regulation was detected in infants with AD and gradually reversed to increased Th1 products (interferon γ/CXCL9/CXCL10/CCL2) in patients with AD from childhood to adulthood. Despite their short disease duration, infants already had evidence of systemic inflammation, with significant upregulation of innate immunity (interleukin 17C/ interleukin-1RN), T-cell activation/migration (CCL19), Th2 (CCL13/CCL17), and Th17 (PI3) proteins. Adults with AD present unique upregulation of cardiovascular proteins related to coagulation and diabetes. LIMITATIONS: Cross-sectional observational study with a single time point.

conclusionSystemic immune signatures of AD are age-specific beyond the shared Th2 immune activation. These data advocate for precision medicine approaches based on age-specific AD profiles.

Indexed as

Dermatitis, AtopicAdolescentAdultChildChild, PreschoolCross-Sectional StudiesHumansInfantInfant, NewbornInflammationProteinsProteomicsTh2 CellsYoung AdultProteinsatopic dermatitisOlinkpediatricproteomic

Identifiers

PMID36773824
PMCPMC10231669
OpenAlexW4319985806

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.