Cited by 42Dermatology and Skin DiseasesFood Allergy and Anaphylaxis ResearchAllergic Rhinitis and Sensitization

Natural history of allergic sensitization in infants with early‐onset atopic dermatitis: results from ORCA Study

Open access
Just, Jocelyne, Deslandes‐Boutmy, Emmanuelle, Amat, Flore, Desseaux, Kristell, Nemni, Ariane, Bourrat, Emmanuelle, Sahraoui, Fatia, Pansé, Isabelle +2 more·2014·Pediatric Allergy and Immunology

Abstract

BACKGROUND: Early-onset atopic dermatitis (AD) is a particular phenotype that may convey a risk of developing multiple sensitizations to allergens but little is known about the pathway of sensitization. The aims of this study were to describe the natural history of sensitization to allergens for this phenotype and to identify the most predictive marker associated with the risk of developing sensitization to inhaled allergens in a well-selected cohort of infants with AD. METHODS: Infants with active AD were enrolled and prospectively explored for biological markers of atopy every year until the age of 6 yr. Allergic sensitization was defined as the presence of positive specific IgEs to allergens and multiple sensitizations as being sensitized to ≥2 allergens. Elevated blood eosinophilia was defined as an eosinophil blood count ≥470 eosinophils/mm(3) and elevated total IgE as a serum IgE level ≥45 kU/l. RESULTS: Two hundred and twenty-nine infants were included. Elevated blood eosinophilia was observed at baseline in 60 children (26.2%) and elevated total IgE in 85 (37.1%). When elevated at baseline, eosinophilia and IgE levels remained significantly higher during the follow-up period. Sensitization to food allergens decreased from 58% to 34%, whereas sensitization to inhaled allergens increased over time from 17% to 67%. Initial multiple sensitizations to food allergens were the most predictive factor for the risk of developing sensitization to inhaled allergens at 6 yr (OR 3.72 [1.68-8.30] p < 0.001). CONCLUSIONS: In the early-onset AD phenotype, multiple sensitization to food allergens conveys a higher risk of sensitization to inhaled allergens than single sensitization.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1111/pai.12287

Cites

1 of 1 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • In the HealthNut study, 5,276 children with AD monitored during the first four years of life demonstrated an increased risk of developing food allergies, such as peanut and egg allergies.

    “In the HealthNut study, 5,276 children with AD were monitored during the first four years of life, demonstrating an increased risk of developing food allergies, such as peanut and egg allergies.”

    From Update on the pathogenesis of atopic dermatitis. (2024) · cites this paper as [13]

    The Abstract describes the ORCA study, which enrolled 229 infants with atopic dermatitis and followed them to age 6—not a HealthNut cohort of 5,276 children followed for four years. The ‘Changes in specific IgEs’ section reports that food-allergen sensitization decreased during follow-up; the paper does not report the claimed increased risk of developing peanut or egg allergy. (LLM, conf=0.88)

    Checked by a reasoning model — may be wrong.

    Experimental — accuracy not yet measured
  • Infants with eczema are exposed to food antigens through the skin, inducing immune cells and producing IgE antibodies (allergic sensitization).

    “Therefore, infants with eczema are exposed to food antigens through the skin, inducing immune cells, and producing IgE antibodies (allergic sensitization).”

    From Update on the pathogenesis of atopic dermatitis. (2024) · cites this paper as [13]

    On p. 356, the paper suggests that allergens enter through the skin in early-onset eczema and describes how they can encounter antigen-presenting cells, initiate a Th2 response, and lead to sensitization. It also links food sensitization to IgE. The citing sentence presents this proposed pathway as an established process for infants with eczema generally, whereas the paper uses qualified language and studies infants with early-onset atopic dermatitis. (LLM, conf=0.85)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 20

  1. Williams H, Stewart A, von Mutius E, Cookson W and Anderson HR. Is eczema really on the increase worldwide? J Allergy Clin Immunol 2008; 121:947-54.
  2. Migueres M, Davila I, Frati F, Azpeita A, Jeanpetit Y, Lhéritier-Barrand M, et al. Types of sensitization to aeroallergens: definitions, prevalences and impact on the diagnosis and treatment of allergic respiratory disease. Clin Tr Allergy 2014; 4:16
  3. Flohr C, Perkin M, Logan K, Marrs T, Radulovic S, Campbell LA, et al. Atopic dermatitis and disease severity are the main risk factors for food sensitization in exclusively breastfed infants. J Invest Dermatol 2014; 134:345-50
  4. Asarnoj A, Ostblom E, Kull I, Lilja G, Pershagen G, Hedin G, et al. Sensitization to inhalant allergens between 4 and 8 years of age is a dynamic process: results friom the BAMSE birth cohort. Clin Exp Allergy 2008; 38: 1507-1513
  5. Silverberg J, Simpson EL. Association between severe eczema in children and multiple comorbid conditions and increased healthcare utilization. Pediatr Allergy Immunol 2013; 24: 476-86
  6. Carlsten C, Dimich-Ward H, Ferguson A, Watson W, Rousseau R, Dybuncio A, et al. Atopic dermatitis in a high-risk cohort: natural history, associated allergic outcomes, and risk factors. Ann Allergy Asthma Immunol 2013; 110:24-8
  7. Williams HC, Burney PG, Pembroke AC, Hay RJ. Validation of the UK diagnostic criteria for atopic dermatitis in a population setting. UK Diagnostic for Atopic Dermatitis Working Party. Br J Dermatol 1996; 135: 12-17
  8. Asher MI, Montefort S, Bjorksten B, Lai CK, Strachan DP, Weiland SK, et al. Worldwide time trends in the prevalence of symptoms of asthma, allergic rhinoconjunctivitis, and eczema in childhood: ISAAC Phase One and Three repeat multicountry cross-sectional surveys. Lancet 2006; 368 (9537): 733-43.
  9. Gelmetti C, Colonna C. The value of SCORAD and beyond. Towards a standardized evaluation of severity? Allergy 2004; 59: 61-65
  10. Just J, Nicoloyanis N, Chauvin M, Pribil C, Grimfeld A, Duru G. Lack of eosinophilia can predict remission in wheezy infants? Clin Exp Allergy 2008; 38: 767- 73
  11. Yamamoto N, Sugiura H, Tanaka K, Uehara M. Heterogeneity of interleukin 5 genetic background in atopic dermatitis patients: significant difference between those with blood eosinophilia and normal eosinophil levels, J Dermatol Sci 2003; 33:121-6
  12. Brown S and Reynolds NJ, Atopic and non-atopic eczema. BMJ 2006; 332:584-8.
  13. Haagerup A, Bjerke T, Schiotz PO, Dahl R, Binderup HG, Tan Q et al. Atopic dermatitis-a total genome-scan for susceptibility genes. Acta Derm Venereol 2004; 84:346-52.
  14. Cork MJ, Danby SG, Vasilopoulos Y, Hadgraft J, Lane ME, Moustafa M et al. Epidermal barrier dysfunction in atopic dermatitis. J Invest Dermatol 2009; 129:892- 1908.
  15. Suárez-Fariñas M, Dhingra N, Gittler J, Shemer A, Cardinale I, de Guzman Strong C et al. Intrinsic atopic dermatitis shows similar TH2 and higher TH17 immune activation compared with extrinsic atopic dermatitis. J Allergy Clin Immunol. 2013; 132:361-70.
  16. Nemoto-Hasebe I, Akiyama M, Nomura T, Sandilands A, McLean WH, Shimizu H. Clinical severity correlates with impaired barrier in filaggrin-related eczema. J Invest Dermatol 2009; 129:682-9.
  17. Hudson TJ. Skin barrier function and allergic risk, Nat Genet 2006; 38:399-400.
  18. Bekkers MB, Aalberse RC, Gehring U, Kerkhof M, Koppelman GH, de Jongste JC et al. Hen's egg, not cow's milk, sensitization in infancy is associated with asthma: 10-year follow-up of the PIAMA birth cohort. J Allergy Clin Immunol 2013; 132:1427- 8.
  19. Just J, Saint-Pierre P, Gouvis-Echraghi R, Laoudi Y, Roufai L, Momas I et al. Childhood allergic asthma is not a single phenotype. J Pediatr 2014; 164:815-20.
  20. Illi S, von Mutius E, Lau S, Nickel R, Gruber C, Niggemann B et al. The natural course of atopic dermatitis from birth to age 7 years and the association with asthma. J Allergy Clin Immunol 2004; 113:925-31.

Cited by

Sorted by citations

Authors
Just, J., Deslandes‐Boutmy, E., Amat, F., Desseaux, K., Nemni, A., Bourrat, E., Sahraoui, F., Pansé, I., Bagot, M., & Fouéré, S.
Affiliations
  • Inserm (FR)
  • Service de biostatistique et informatique médicale Hôpital Saint‐Louis, INSERM, U 717 Université Paris 7 Paris France
  • Hôpital Armand-Trousseau (FR)
  • Assistance Publique – Hôpitaux de Paris (FR)
Corresponding author
Just, Jocelyne
Venue
Pediatric Allergy and Immunology
Publisher
Wiley
Published
2014-11
Volume
25
Issue
7
Pages
668-673
ISSN
  • 0905-6157 (ISSN-L)
  • 1399-3038
OpenAlex
W2016672520
Cited by
42
References
1
Citations by year
2026: 1 · 2025: 1 · 2024: 3 · 2023: 1 · 2022: 6 · 2021: 1 · 2020: 1 · 2019: 3 · 2018: 3 · 2017: 5 · 2016: 9 · 2015: 8
FWCI
8.02
Type
journal article
Language
en
Locations
  • Pediatric Allergy and Immunology (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion, other-oa)
Topics
  • Health Sciences › Medicine › Dermatology › Dermatology and Skin Diseases
  • Health Sciences › Medicine › Immunology and Allergy › Food Allergy and Anaphylaxis Research
  • Health Sciences › Medicine › Immunology and Allergy › Allergic Rhinitis and Sensitization
Keywords
early-onset atopic dermatitis, allergen sensitization, infants, food sensitization, multiple sensitization, peripheral eosinophilia, total IgE, natural history (disease), predictive biomarkers
MeSH terms
Allergens, Child, Child, Preschool, Dermatitis, Atopic, Eosinophilia, Female, Follow-Up Studies, Food, Food Hypersensitivity, Humans, Immunoglobulin E, Immunization, Infant, Infant, Newborn, Male, Medical History Taking, Prospective Studies, Cohort Studies, Age of Onset

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review