Atopic endotype in childhood

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Standard

Atopic endotype in childhood. / Schoos, Ann-Marie Malby; Chawes, Bo Lund Krogsgaard; Rasmussen, Morten Arendt; Bloch, Joakim; Bønnelykke, Klaus; Bisgaard, Hans.

I: Journal of Allergy and Clinical Immunology, Bind 137, Nr. 3, 2016, s. 844-851.e4.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Schoos, A-MM, Chawes, BLK, Rasmussen, MA, Bloch, J, Bønnelykke, K & Bisgaard, H 2016, 'Atopic endotype in childhood', Journal of Allergy and Clinical Immunology, bind 137, nr. 3, s. 844-851.e4. https://doi.org/10.1016/j.jaci.2015.10.004

APA

Schoos, A-M. M., Chawes, B. L. K., Rasmussen, M. A., Bloch, J., Bønnelykke, K., & Bisgaard, H. (2016). Atopic endotype in childhood. Journal of Allergy and Clinical Immunology, 137(3), 844-851.e4. https://doi.org/10.1016/j.jaci.2015.10.004

Vancouver

Schoos A-MM, Chawes BLK, Rasmussen MA, Bloch J, Bønnelykke K, Bisgaard H. Atopic endotype in childhood. Journal of Allergy and Clinical Immunology. 2016;137(3):844-851.e4. https://doi.org/10.1016/j.jaci.2015.10.004

Author

Schoos, Ann-Marie Malby ; Chawes, Bo Lund Krogsgaard ; Rasmussen, Morten Arendt ; Bloch, Joakim ; Bønnelykke, Klaus ; Bisgaard, Hans. / Atopic endotype in childhood. I: Journal of Allergy and Clinical Immunology. 2016 ; Bind 137, Nr. 3. s. 844-851.e4.

Bibtex

@article{4b396c391ca04a278749b19b064207f2,
title = "Atopic endotype in childhood",
abstract = "Background: The term atopic disorder is an early attempt to define specific endotypes of children with asthma, eczema, or both and increased IgE levels.Objective: We performed a longitudinal analysis of the relevance of the atopic endotype from birth to age 13 years.Methods: Allergic sensitization against 28 inhalant and food allergens was assessed at ½, 1½, 4, 6, and 13 years of age in 399 children from the Copenhagen Prospective Study on Asthma in Childhood2000 birth cohort by using both skin prick test responses and specific IgE levels. Asthma and eczema were diagnosed longitudinally by strictly adhering to predefined algorithms. Associations between allergic sensitization, asthma, and eczema were estimated by means of logistic regression, and a machine learning approach was used to identify temporal phenotype clusters of these traits.Results: Allergic sensitization showed no association with asthma through early childhood (0-6 years) when analyzed as any sensitization (odds ratio [OR] range, 0.78-1.29; P ≥ .48). However, at 13 years of age, any sensitization was associated with asthma (OR range, 4.02-5.94; all P < .001). In contrast, any sensitization was associated with eczema at ½, 1½, and 6 years of age (OR range, 2.06-6.02; P ≤ .01) and borderline associated at 4 years of age (OR, 1.61 [95% CI, 0.96-2.69]; P = .07) but not at 13 years of age (OR, 1.57 [95% CI, 0.78-3.16]; P = .21). We identified 4 latent patterns of disease development that were either dominated by sensitization (37%), eczema (26%), asthma (14%), or healthy status (24%).Conclusion: We found very little interdependency between asthma, eczema, and allergic sensitization through childhood. The associations between those entities were strongly dependent on age, type of allergens, and method of testing for sensitization. Therefore, atopy in children is unlikely to represent a true endotype.",
keywords = "Endotype, sensitization, skin prick test, specific IgE, eczema, asthma, children",
author = "Schoos, {Ann-Marie Malby} and Chawes, {Bo Lund Krogsgaard} and Rasmussen, {Morten Arendt} and Joakim Bloch and Klaus B{\o}nnelykke and Hans Bisgaard",
year = "2016",
doi = "10.1016/j.jaci.2015.10.004",
language = "English",
volume = "137",
pages = "844--851.e4",
journal = "Journal of Allergy and Clinical Immunology",
issn = "0091-6749",
publisher = "Mosby Inc.",
number = "3",

}

RIS

TY - JOUR

T1 - Atopic endotype in childhood

AU - Schoos, Ann-Marie Malby

AU - Chawes, Bo Lund Krogsgaard

AU - Rasmussen, Morten Arendt

AU - Bloch, Joakim

AU - Bønnelykke, Klaus

AU - Bisgaard, Hans

PY - 2016

Y1 - 2016

N2 - Background: The term atopic disorder is an early attempt to define specific endotypes of children with asthma, eczema, or both and increased IgE levels.Objective: We performed a longitudinal analysis of the relevance of the atopic endotype from birth to age 13 years.Methods: Allergic sensitization against 28 inhalant and food allergens was assessed at ½, 1½, 4, 6, and 13 years of age in 399 children from the Copenhagen Prospective Study on Asthma in Childhood2000 birth cohort by using both skin prick test responses and specific IgE levels. Asthma and eczema were diagnosed longitudinally by strictly adhering to predefined algorithms. Associations between allergic sensitization, asthma, and eczema were estimated by means of logistic regression, and a machine learning approach was used to identify temporal phenotype clusters of these traits.Results: Allergic sensitization showed no association with asthma through early childhood (0-6 years) when analyzed as any sensitization (odds ratio [OR] range, 0.78-1.29; P ≥ .48). However, at 13 years of age, any sensitization was associated with asthma (OR range, 4.02-5.94; all P < .001). In contrast, any sensitization was associated with eczema at ½, 1½, and 6 years of age (OR range, 2.06-6.02; P ≤ .01) and borderline associated at 4 years of age (OR, 1.61 [95% CI, 0.96-2.69]; P = .07) but not at 13 years of age (OR, 1.57 [95% CI, 0.78-3.16]; P = .21). We identified 4 latent patterns of disease development that were either dominated by sensitization (37%), eczema (26%), asthma (14%), or healthy status (24%).Conclusion: We found very little interdependency between asthma, eczema, and allergic sensitization through childhood. The associations between those entities were strongly dependent on age, type of allergens, and method of testing for sensitization. Therefore, atopy in children is unlikely to represent a true endotype.

AB - Background: The term atopic disorder is an early attempt to define specific endotypes of children with asthma, eczema, or both and increased IgE levels.Objective: We performed a longitudinal analysis of the relevance of the atopic endotype from birth to age 13 years.Methods: Allergic sensitization against 28 inhalant and food allergens was assessed at ½, 1½, 4, 6, and 13 years of age in 399 children from the Copenhagen Prospective Study on Asthma in Childhood2000 birth cohort by using both skin prick test responses and specific IgE levels. Asthma and eczema were diagnosed longitudinally by strictly adhering to predefined algorithms. Associations between allergic sensitization, asthma, and eczema were estimated by means of logistic regression, and a machine learning approach was used to identify temporal phenotype clusters of these traits.Results: Allergic sensitization showed no association with asthma through early childhood (0-6 years) when analyzed as any sensitization (odds ratio [OR] range, 0.78-1.29; P ≥ .48). However, at 13 years of age, any sensitization was associated with asthma (OR range, 4.02-5.94; all P < .001). In contrast, any sensitization was associated with eczema at ½, 1½, and 6 years of age (OR range, 2.06-6.02; P ≤ .01) and borderline associated at 4 years of age (OR, 1.61 [95% CI, 0.96-2.69]; P = .07) but not at 13 years of age (OR, 1.57 [95% CI, 0.78-3.16]; P = .21). We identified 4 latent patterns of disease development that were either dominated by sensitization (37%), eczema (26%), asthma (14%), or healthy status (24%).Conclusion: We found very little interdependency between asthma, eczema, and allergic sensitization through childhood. The associations between those entities were strongly dependent on age, type of allergens, and method of testing for sensitization. Therefore, atopy in children is unlikely to represent a true endotype.

KW - Endotype

KW - sensitization

KW - skin prick test

KW - specific IgE

KW - eczema

KW - asthma

KW - children

U2 - 10.1016/j.jaci.2015.10.004

DO - 10.1016/j.jaci.2015.10.004

M3 - Journal article

C2 - 26597163

VL - 137

SP - 844-851.e4

JO - Journal of Allergy and Clinical Immunology

JF - Journal of Allergy and Clinical Immunology

SN - 0091-6749

IS - 3

ER -

ID: 164321428