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Genomic architecture of asthma differs by sex.
Mersha, Tesfaye B; Martin, Lisa J; Biagini Myers, Jocelyn M; Kovacic, Melinda Butsch; He, Hua; Lindsey, Mark; Sivaprasad, Umasundari; Chen, Weiguo; Khurana Hershey, Gurjit K.
Afiliação
  • Mersha TB; Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Electronic address: tesfaye.mersha@cchmc.org.
  • Martin LJ; Division of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Electronic address: martin@cchmc.org.
  • Biagini Myers JM; Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Electronic address: jocelyn.biagini.myers@cchmc.org.
  • Kovacic MB; Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Electronic address: melinda.butsch.kovacic@cchmc.org.
  • He H; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Electronic address: hua.he@cchmc.org.
  • Lindsey M; Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Electronic address: mark.lindsey@cchmc.org.
  • Sivaprasad U; Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Electronic address: umasundari.sivaprasad@cchmc.org.
  • Chen W; Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Electronic address: weiguo.chen@cchmc.org.
  • Khurana Hershey GK; Division of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA. Electronic address: gurjit.hershey@cchmc.org.
Genomics ; 106(1): 15-22, 2015 Jul.
Article em En | MEDLINE | ID: mdl-25817197
Asthma comprised of highly heterogeneous subphenotypes resulting from complex interplay between genetic and environmental stimuli. While much focus has been placed on extrinsic environmental stimuli, intrinsic environment such as sex can interact with genes to influence asthma risk. However, few studies have examined sex-specific genetic effects. The overall objective of this study was to evaluate if sex-based differences exist in genomic associations with asthma. We tested 411 asthmatics and 297 controls for presence of interactions and sex-stratified effects in 51 genes using both SNP and gene expression data. Logistic regression was used to test for association. Over half (55%) of the genetic variants identified in sex-specific analyses were not identified in the sex-combined analysis. Further, sex-stratified genetic analyses identified associations with significantly higher median effect sizes than sex-combined analysis for girls (p-value=6.5E-15) and for boys (p-value=1.0E-7). When gene expression data were analyzed to identify genes that were differentially expressed in asthma versus non-asthma, nearly one third (31%) of the probes identified in the sex-specific analyses were not identified in the sex-combined analysis. Both genetic and gene expression data suggest that the biologic underpinnings for asthma may differ by sex. Failure to recognize sex interactions in asthma greatly decreases the ability to detect significant genomic variation and may result in significant misrepresentation of genes and pathways important in asthma in different environments.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma Tipo de estudo: Prognostic_studies Limite: Child / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma Tipo de estudo: Prognostic_studies Limite: Child / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article