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PDE11A associations with asthma: results of a genome-wide association scan.

机译:PDE11A与哮喘的关联:全基因组关联扫描的结果。

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摘要

The results of 4 successful genome-wide association studies have been reported recently, yielding 4 distinct loci, 0RMDL3, CHI3L1, PDE4D, and DENNDIB,1'4 with the disparity in the results likely caused by differences in the phenotypes studied. In an attempt to dissect further the genetic network in complex asthmatic phenotypes, we investigated allergic asthma specifically defined in children at age 6 years. Cases were patients with allergic asthma with early-onset persistent asthma defined as having physician diagnosed asthma and wheeze at ages 1 and 6 years and asthma medication use and allergies as reported by the mother; controls were defined as those having no diagnosis of asthma or reactive airway disease and no symptoms at ages 1 or 6 years and no asthma meditation use and no allergies (see Definition of Cases and Controls section in the Online Repository at www. jacionline.org for additional recruitment details and Table El for demographic and phenotype data).
机译:最近已经报道了4个成功的全基因组关联研究的结果,产生了4个不同的基因座,0RMDL3,CHI3L1,PDE4D和DENNDIB,1'4,结果的差异可能是由于所研究表型的差异所致。为了进一步剖析复杂哮喘表型的遗传网络,我们研究了在6岁儿童中明确定义的过敏性哮喘。病例为患有过敏性哮喘并伴有早发性持续性哮喘的患者,其定义是医生诊断为1岁和6岁时患有哮喘和喘息,并且母亲报告了哮喘药物的使用和过敏情况;对照被定义为那些没有诊断出哮喘或反应性气道疾病,在1或6岁时没有症状,没有使用哮喘进行冥想并且没有过敏的对照(参见www.jacionline.org在线存储库中的“病例和对照的定义”部分,其他招聘详细信息以及有关人口统计学和表型数据的表El)。

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