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Clinical onset of atopic eczema: Results from 2 nationally representative British birth cohorts followed through midlife.
Abuabara, Katrina; Ye, Morgan; McCulloch, Charles E; Sullivan, Alice; Margolis, David J; Strachan, David P; Paternoster, Lavinia; Yew, Yik Weng; Williams, Hywel C; Langan, Sinéad M.
Affiliation
  • Abuabara K; Program for Clinical Research, Department of Dermatology, University of California, San Francisco School of Medicine, San Francisco, Calif. Electronic address: Katrina.abuabara@ucsf.edu.
  • Ye M; Program for Clinical Research, Department of Dermatology, University of California, San Francisco School of Medicine, San Francisco, Calif.
  • McCulloch CE; Division of Biostatistics, University of California, San Francisco School of Medicine, San Francisco, Calif.
  • Sullivan A; UCL Institute of Education, University College, London, United Kingdom.
  • Margolis DJ; Department of Dermatology and Center for Epidemiology and Biostatistics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pa.
  • Strachan DP; Population Health Research Institute, St George's University of London, London, United Kingdom.
  • Paternoster L; MRC Integrative Epidemiology Unit, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
  • Yew YW; National Skin Centre, Singapore.
  • Williams HC; Centre of Evidence Based Dermatology, Faculty of Medicine & Health Sciences, University of Nottingham, Nottingham, United Kingdom.
  • Langan SM; Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.
J Allergy Clin Immunol ; 144(3): 710-719, 2019 09.
Article in En | MEDLINE | ID: mdl-31260715
ABSTRACT

BACKGROUND:

Atopic eczema onset is described primarily in early childhood, and the frequency and characteristics of adult-onset disease remain controversial.

OBJECTIVE:

We sought to determine the proportion of subjects who report atopic eczema symptoms between birth and midadulthood and to examine demographic, immunologic, and genetic factors associated with period of symptom onset.

METHODS:

We conducted a longitudinal study using data from 2 nationally representative community-based birth cohorts from the United Kingdom the British Cohort Studies 1958 and 1970. Subjects were followed from birth through age 42 to 50 years. The primary outcome was the age period of self-reported atopic eczema symptom onset based on repeated measures of self-reported atopic eczema at each survey wave.

RESULTS:

The annual period prevalence of atopic eczema ranged from 5% to 15% in 2 cohorts of more than 17,000 participants each followed from birth through middle age. There was no clear trend in prevalence by age, and among adults reporting active atopic eczema during a given year, only 38% had symptom onset reported in childhood. When compared with subjects whose eczema started in childhood, those with adult-onset disease were more likely to be women, from Scotland or Northern England, of lower childhood socioeconomic group, smokers in adulthood, and less likely to have a history of asthma. In a subanalysis using data from the 1958 cohort only, genetic mutations previously associated with atopic eczema, including filaggrin-null mutations, and allergen-specific IgE were more common among those with childhood-onset disease.

CONCLUSION:

Rates of self-reported atopic eczema remain high after childhood, and adult-onset atopic eczema has different risk factor associations than childhood-onset eczema.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dermatitis, Atopic Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn Country/Region as subject: Europa Language: En Journal: J Allergy Clin Immunol Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dermatitis, Atopic Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn Country/Region as subject: Europa Language: En Journal: J Allergy Clin Immunol Year: 2019 Document type: Article
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