Evidence map›Paper›PMID 34673050›Full record

ArticleThe Journal of allergy and clinical immunology2022

Longitudinal atopic dermatitis endotypes: An atopic march paradigm that includes Black children.

Jocelyn M Biagini, John W Kroner, Asel Baatyrbek Kyzy, Alexandra Gonzales, Hua He, Mariana Stevens, Brittany Grashel, Daniel Spagna, Samuel Paul, Rahul Patel and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of allergy and clinical immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
8.0field-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

33 citing papers in PubMed, 51 citations in OpenAlex.

  1. Associations between genetic ancestry and allergic outcomes at 10 years among Black children.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2026
    Article
  2. Article
  3. Genome-wide cross-trait analysis of heterogeneous outcomes in early life atopic dermatitis.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2025
    Article
  4. Article
  5. Socioeconomic deprivation performs equally to race in the Pediatric Asthma Risk Score.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Reducing disparities in the care of atopic dermatitis.Archives of dermatological research · 2024
    Review
  13. Article
  14. Article
  15. Article
  16. Genetic and Immunological Pathogenesis of Atopic Dermatitis.The Journal of investigative dermatology · 2024
    Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 2 institutions in 1 country.

Jocelyn M BiaginiDivision of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
John W KronerDivision of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Asel Baatyrbek KyzyDivision of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Alexandra GonzalesDivision of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Hua HeDivision of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Mariana StevensDivision of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Brittany GrashelDivision of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Daniel SpagnaDivision of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Samuel PaulDivision of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Rahul PatelDivision of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Angelo BucciDivision of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Michael G SherenianDivision of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Liza Bronner MurrisonDivision of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Lisa J MartinDivision of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Gurjit K Khurana HersheyDivision of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio. Electronic address: gurjit.hershey@cchmc.org.
Cincinnati Children's Hospital Medical Center · USUniversity of Cincinnati Medical Center · US

Funding

TSLP, IL-9-producing mucosal mast cells, and allergic inflammationU19AI070235 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI Gurjit K. Khurana Hershey · 2006 to 2026
$31.3M
NIAID NIH HHS U19 AI070235
6 · The paper itself

Abstract

backgroundThe atopic march has been studied mostly in White populations, biasing our current paradigms.

objectiveWe sought to define the atopic march in Black and White children and explore mechanisms for racial differences.

methodsUtilizing the Mechanisms of Progression of Atopic Dermatitis to Asthma in Children (MPAACH) cohort (n = 601), we assessed longitudinal sensitization, food allergy (FA), allergic rhinitis, risk of asthma development (through the Pediatric Asthma Risk Score), Scoring for Atopic Dermatitis (SCORAD), transepidermal water loss, skin filaggrin (FLG) expression, exposures, and genetic heritability to define AD progression endotypes in Black and White children.

resultsWhite MPAACH children were more likely to be sensitized to aero and food allergens (P = .0001) and over 3 times more likely to develop FA and/or allergic rhinitis (AR) without asthma risk (P < .0001). In contrast, Black children were over 6 times more likely to proceed to high asthma risk without FA, sensitization, or AR (P < .0001). White children had higher lesional and nonlesional transepidermal water loss (both P < .001) as well as decreased nonlesional keratinocyte FLG expression (P = .02). Black children had increased genetic heritability for asthma risk and higher rates of exposures to secondhand smoke and traffic-related air pollution.

conclusionsBlack and White children with AD have distinct allergic trajectories defined by different longitudinal endotypes. Black children exhibit higher asthma risk despite a more intact skin barrier and less sensitization, FA, and AR. White children have less asthma risk, despite a more dysfunctional skin barrier, and more FA, AR, and sensitization. The observed racial differences are likely due in part to increased genetic heritability for asthma risk and harmful environmental exposures in Black children. Collectively, our findings provide a new paradigm for an atopic march that is inclusive of Black children.

Indexed as

AsthmaDermatitis, AtopicFood HypersensitivityRhinitis, AllergicChildHumansWaterWateratopic dermatitisAtopic marchbiomarkerenvironmental exposuregenetic ancestryraceskin barrier

Identifiers

PMID34673050
PMCPMC9275099
OpenAlexW3207146126

What Socratic 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 Socratic graph.