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Quantitative linkage genome scan for atopy in a large collection of Caucasian families.

机译:大量的白种人家庭中的定量连锁基因组扫描检测特应性。

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Quantitative phenotypes correlated with a complex disorder offer increased power to detect linkage in comparison to affected-unaffected classifications. Asthma is a complex disorder characterized by periods of bronchial obstruction and increased bronchial hyper reactivity. In childhood and early adulthood, asthma is frequently associated also with quantitative measures of atopy. Genome wide quantitative multipoint linkage analysis was conducted for serum IgE levels and percentage of positive skin prick test (SPT(per)) using three large groups of families originally ascertained for asthma. In this report, 438 and 429 asthma families were informative for linkage using IgE and SPT(per) which represents 690 independent families. Suggestive linkage (LOD >/= 2) was found on chromosomes 1, 3, and 8q with maximum LODs of 2.34 (IgE), 2.03 (SPT(per)), and 2.25 (IgE) near markers D1S1653, D3S2322-D3S1764, and D8S2324, respectively. The results from chromosomes 1 and 3 replicate previous reports of linkage. We also replicate linkage to 5q with peak LODs of 1.96 (SPT(per)) and 1.77 (IgE) at or near marker D5S1480. Our results provide further evidence implicating chromosomes 1, 3, and 5q. The current report represents one of the biggest genome scans so far reported for asthma related phenotypes. This study also demonstrates the utility of increased sample sizes and quantitative phenotypes in linkage analysis of complex disorders.
机译:与未受影响的分类相比,与复杂疾病相关的定量表型提供了更高的检测连锁的能力。哮喘是一种复杂的疾病,以支气管阻塞和支气管高反应性增加为特征。在儿童期和成年早期,哮喘也经常与特应性的定量检测有关。使用三组最初确定为哮喘的家庭,对全基因组进行了血清全基因组定量多点连锁分析,以测定血清IgE水平和皮肤点刺试验阳性率(SPT(per))。在此报告中,代表690个独立家庭的438个和429个哮喘家庭使用IgE和SPT(per)进行了关联,从而获得了很多信息。在染色体1、3和8q上发现暗示性连锁(LOD> / = 2),在标记D1S1653,D3S2322-D3S1764和D1S1653附近的最大LOD为2.34(IgE),2.03(SPT(per))和2.25(IgE)。分别为D8S2324。染色体1和3的结果重复了以前的连锁报道。我们还在标记D5S1480或附近复制了与5q的连锁,峰值LOD为1.96(SPT(per))和1.77(IgE)。我们的结果提供了进一步的证据,暗示了染色体1、3和5q。本报告代表了迄今为止与哮喘相关的表型报道的最大的基因组扫描之一。这项研究还证明了在复杂疾病的连锁分析中增加样本量和定量表型的实用性。

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