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The nasal methylome and childhood atopic asthma.
Yang, Ivana V; Pedersen, Brent S; Liu, Andrew H; O'Connor, George T; Pillai, Dinesh; Kattan, Meyer; Misiak, Rana Tawil; Gruchalla, Rebecca; Szefler, Stanley J; Khurana Hershey, Gurjit K; Kercsmar, Carolyn; Richards, Adam; Stevens, Allen D; Kolakowski, Christena A; Makhija, Melanie; Sorkness, Christine A; Krouse, Rebecca Z; Visness, Cynthia; Davidson, Elizabeth J; Hennessy, Corinne E; Martin, Richard J; Togias, Alkis; Busse, William W; Schwartz, David A.
Afiliação
  • Yang IV; Department of Medicine and University of Colorado, School of Medicine, Aurora, Colo; National Jewish Health, Denver, Colo; Department of Epidemiology, Colorado School of Public Health, Aurora, Colo. Electronic address: ivana.yang@ucdenver.edu.
  • Pedersen BS; Department of Medicine and University of Colorado, School of Medicine, Aurora, Colo.
  • Liu AH; National Jewish Health, Denver, Colo.
  • O'Connor GT; Department of Medicine, Boston University School of Medicine, Boston, Mass.
  • Pillai D; Children's National Health System, Washington, DC.
  • Kattan M; Columbia University Medical Center, New York, NY.
  • Misiak RT; Department of Medicine, Henry Ford Hospital, Detroit, Mich.
  • Gruchalla R; University of Texas, Southwestern Medical Center, Dallas, Tex.
  • Szefler SJ; Department of Pediatrics, Children's Hospital Colorado and University of Colorado, School of Medicine, Aurora, Colo.
  • Khurana Hershey GK; Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Kercsmar C; Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Richards A; Department of Medicine and University of Colorado, School of Medicine, Aurora, Colo.
  • Stevens AD; National Jewish Health, Denver, Colo.
  • Kolakowski CA; National Jewish Health, Denver, Colo.
  • Makhija M; Children's Hospital of Chicago, Chicago, Ill.
  • Sorkness CA; Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, Wis.
  • Krouse RZ; Rho Federal Systems Division, Chapel Hill, NC.
  • Visness C; Rho Federal Systems Division, Chapel Hill, NC.
  • Davidson EJ; Department of Medicine and University of Colorado, School of Medicine, Aurora, Colo.
  • Hennessy CE; Department of Medicine and University of Colorado, School of Medicine, Aurora, Colo.
  • Martin RJ; National Jewish Health, Denver, Colo.
  • Togias A; National Institute of Allergy and Infectious Diseases, Bethesda, Md; and University of Colorado, Aurora, CO.
  • Busse WW; Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, Wis.
  • Schwartz DA; Department of Medicine and University of Colorado, School of Medicine, Aurora, Colo; National Jewish Health, Denver, Colo; Department of Immunology, University of Colorado, Aurora, Colo. Electronic address: david.schwartz@ucdenver.edu.
J Allergy Clin Immunol ; 139(5): 1478-1488, 2017 May.
Article em En | MEDLINE | ID: mdl-27745942
ABSTRACT

BACKGROUND:

Given the strong environmental influence on both epigenetic marks and allergic asthma in children, the epigenetic alterations in respiratory epithelia might provide insight into allergic asthma.

OBJECTIVE:

We sought to identify DNA methylation and gene expression changes associated with childhood allergic persistent asthma.

METHODS:

We compared genomic DNA methylation patterns and gene expression in African American children with persistent atopic asthma (n = 36) versus healthy control subjects (n = 36). Results were validated in an independent population of asthmatic children (n = 30) by using a shared healthy control population (n = 36) and in an independent population of white adult atopic asthmatic patients (n = 12) and control subjects (n = 12).

RESULTS:

We identified 186 genes with significant methylation changes, differentially methylated regions or differentially methylated probes, after adjustment for age, sex, race/ethnicity, batch effects, inflation, and multiple comparisons. Genes differentially methylated included those with established roles in asthma and atopy and genes related to extracellular matrix, immunity, cell adhesion, epigenetic regulation, and airflow obstruction. The methylation changes were substantial (median, 9.5%; range, 2.6% to 29.5%). Hypomethylated and hypermethylated genes were associated with increased and decreased gene expression, respectively (P < 2.8 × 10-6 for differentially methylated regions and P < 7.8 × 10-10 for differentially methylated probes). Quantitative analysis in 53 differentially expressed genes demonstrated that 32 (60%) have significant methylation-expression relationships within 5 kb of the gene. Ten loci selected based on the relevance to asthma, magnitude of methylation change, and methylation-expression relationships were validated in an independent cohort of children with atopic asthma. Sixty-seven of 186 genes also have significant asthma-associated methylation changes in nasal epithelia of adult white asthmatic patients.

CONCLUSIONS:

Epigenetic marks in respiratory epithelia are associated with allergic asthma and gene expression changes in inner-city children.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Metilação de DNA / Mucosa Nasal Limite: Adult / Aged / Aged80 / Child / Female / Humans / Male / Middle aged Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Metilação de DNA / Mucosa Nasal Limite: Adult / Aged / Aged80 / Child / Female / Humans / Male / Middle aged Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2017 Tipo de documento: Article