Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2009-9-2
pubmed:abstractText
Sex differences in asthma-associated phenotypes are well known but the genetic factors that may account for these differences have received little attention. This study aimed to characterize sex-specific and pleiotropic genetic factors underlying four quantitative phenotypes involved in the main asthma physiopathological pathways: immunoglobulin E levels, a measure of polysensitization (SPTQ), eosinophil counts and a measure of lung function FEV(1)/H(2) (forced expiratory volume in one second divided by height square). Sex-stratified univariate and bivariate linkage analyses were conducted in 295 families from the Epidemiological study on the Genetics and Environment of Asthma study. We found genome-wide significant evidence for a male-specific pleiotropic QTL (quantitative trait loci) on 5q31 (P=7 x 10(-9)) influencing both FEV(1)/H(2) and SPTQ and for a female-specific pleiotropic QTL on 11q23 underlying SPTQ and immunoglobulin E (P=2 x 10(-5)). Three other sex-specific regions of linkage were detected for eosinophil: 4q24 and 22q13 in females, and 3p25 in males. Further, bivariate association analysis of FEV(1)/H(2) and SPTQ with 5q31 candidate genes in males showed a significant association with two single-nucleotide polymorphisms within IL9 gene, rs2069885 and rs2069882 (P=0.02 and P=0.002, respectively, after Bonferroni's correction). This study underlies the importance of taking into account complex mechanisms, such as heterogeneity according to sex and pleiotropy to unravel the genes involved in asthma phenotypes.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1476-5470
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
10
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
559-65
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:19536153-Adolescent, pubmed-meshheading:19536153-Asthma, pubmed-meshheading:19536153-Bronchial Hyperreactivity, pubmed-meshheading:19536153-Cell Count, pubmed-meshheading:19536153-Child, pubmed-meshheading:19536153-Chromosome Mapping, pubmed-meshheading:19536153-Chromosomes, Human, Pair 11, pubmed-meshheading:19536153-Chromosomes, Human, Pair 22, pubmed-meshheading:19536153-Chromosomes, Human, Pair 4, pubmed-meshheading:19536153-Eosinophils, pubmed-meshheading:19536153-Female, pubmed-meshheading:19536153-Forced Expiratory Volume, pubmed-meshheading:19536153-Genetic Linkage, pubmed-meshheading:19536153-Genome, Human, pubmed-meshheading:19536153-Genome-Wide Association Study, pubmed-meshheading:19536153-Genotype, pubmed-meshheading:19536153-Humans, pubmed-meshheading:19536153-Immunoglobulin E, pubmed-meshheading:19536153-Interleukin-9, pubmed-meshheading:19536153-Lung, pubmed-meshheading:19536153-Male, pubmed-meshheading:19536153-Microsatellite Repeats, pubmed-meshheading:19536153-Phenotype, pubmed-meshheading:19536153-Polymorphism, Single Nucleotide, pubmed-meshheading:19536153-Quantitative Trait Loci, pubmed-meshheading:19536153-Respiratory Function Tests, pubmed-meshheading:19536153-Sex Factors
pubmed:year
2009
pubmed:articleTitle
Sex-specific effect of IL9 polymorphisms on lung function and polysensitization.
pubmed:affiliation
INSERM, U946, Fondation Jean Dausset/CEPH, Paris 75010, France. hugues.aschard@inserm.fr
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't