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Genetic ancestry does not explain increased atopic dermatitis susceptibility or worse disease control among African American subjects in 2 large US cohorts.
Abuabara, Katrina; You, Yue; Margolis, David J; Hoffmann, Thomas J; Risch, Neil; Jorgenson, Eric.
  • Abuabara K; Program for Clinical Research, Department of Dermatology, University of California, San Francisco, Calif. Electronic address: Katrina.abuabara@ucsf.edu.
  • You Y; Division of Biostatistics and Epidemiology, University of California, Berkeley, Calif.
  • Margolis DJ; Department of Dermatology and Center for Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pa.
  • Hoffmann TJ; Institute for Human Genetics and Department of Epidemiology and Biostatistics, University of California, San Francisco, Calif.
  • Risch N; Institute for Human Genetics and Department of Epidemiology and Biostatistics, University of California, San Francisco, Calif; Division of Research, Kaiser Permanente, Oakland, Calif.
  • Jorgenson E; Division of Research, Kaiser Permanente, Oakland, Calif.
J Allergy Clin Immunol ; 145(1): 192-198.e11, 2020 01.
Article en En | MEDLINE | ID: mdl-31369801
ABSTRACT

BACKGROUND:

Atopic dermatitis (AD) is more common among African American children. Whether there are racial/ethnic difference among adults with AD and the causes for those disparities are unclear.

OBJECTIVE:

We sought to examine the relationship between self-reported race/ethnicity and AD and determine whether African genetic ancestry is predictive of these outcomes among African American subjects.

METHODS:

We analyzed data from 2 independent multiethnic longitudinal studies 86,893 subjects aged 18 to 100 years from the Kaiser Permanente Genetic Epidemiology Research on Adult Health and Aging (GERA) cohort and 5467 subjects aged 2 to 26 years from the national Pediatric Eczema Elective Registry (PEER) cohort. The primary outcomes were physician-diagnosed AD in GERA and repeated measures of self-reported disease control among patients with physician-diagnosed AD at 6-month intervals in PEER. We examined whether self-identified African American race/ethnicity was predictive of these outcomes and then tested whether a continuous measure of African genetic ancestry was associated with outcomes within the African American group.

RESULTS:

AD was more common among self-identified African American subjects than non-Hispanic white subjects in GERA (4.4% vs 2.1%; odds ratio, 2.06; 95% CI, 1.70-2.48) and less well-controlled in PEER subjects (odds of 1-level worse control, 1.91; 95% CI, 1.64-2.22). However, African genetic ancestry was not associated with AD risk or control among self-identified African American subjects in either cohort, nor did an AD polygenic risk score or genetic skin pigment score explain the AD disparities in patients with AD.

CONCLUSION:

Ancestry-related genetic effects do not explain increased AD prevalence or poorer disease control among African American subjects.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Negro o Afroamericano / Dermatitis Atópica Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged País como asunto: America do norte Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Negro o Afroamericano / Dermatitis Atópica Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged País como asunto: America do norte Idioma: En Año: 2020 Tipo del documento: Article