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哮喘和特应性特征的因子分析显示有两个主要成分,其中一个与5号染色体q臂上的标记有关。

Factor analysis of asthma and atopy traits shows 2 major components, one of which is linked to markers on chromosome 5q.

作者信息

Holberg C J, Halonen M, Solomon S, Graves P E, Baldini M, Erickson R P, Martinez F D

机构信息

Arizona Respiratory Center and the Department of Pediatrics, University of Arizona Health Sciences Center, Tucson 85724, USA.

出版信息

J Allergy Clin Immunol. 2001 Nov;108(5):772-80. doi: 10.1067/mai.2001.119158.

Abstract

BACKGROUND

A variety of definitions of asthma and atopy traits have been used in genetic studies. The variables used may be correlated, increasing the likelihood of type I error.

OBJECTIVE

We sought to clarify and quantify phenotypes that may be characterized by related traits. Principal components and factor analysis were applied to the correlation matrix of asthma and atopy traits before linkage analysis.

METHODS

Factor analysis was performed on 468 Hispanic and non-Hispanic white children enrolled in the Tucson Children's Respiratory Study, with complete information on 24 items, including skin test response to 7 allergens, total serum IgE levels, presence or absence of asthma attacks, wheezing episodes, hay fever, and cough. Factor score coefficients were then applied to all siblings (n = 877), and quantitative factor scores were derived. Single-point and multipoint nonparametric sib-pair analyses were performed to assess linkage to markers on chromosome 5q31-33. Analyses were also performed for individual items.

RESULTS

Two main factors were identified: Factor I had high loadings on atopic items, including skin test responses, IgE, and hay fever, and Factor II had high loadings that included asthma diagnosis, wheezing, cough, and Alternaria species skin test response. Factors I and II were correlated at an r value of 0.19. For the quantitative factor scores, significant single-point linkage (P < .0001) was demonstrated only for atopic Factor I, and a peak multipoint LOD score of 2.7 was seen for marker D5S479. Multipoint LOD scores for individual items were 1.1 or less.

CONCLUSION

These analyses suggest evidence for a locus or loci mapping to chromosome 5q31-33 associated with this composite atopic phenotype.

摘要

背景

在基因研究中,哮喘和特应性特征有多种定义。所使用的变量可能相互关联,增加了I型错误的可能性。

目的

我们试图阐明并量化可能由相关特征所表征的表型。在连锁分析之前,将主成分分析和因子分析应用于哮喘和特应性特征的相关矩阵。

方法

对参加图森儿童呼吸研究的468名西班牙裔和非西班牙裔白人儿童进行因子分析,这些儿童有关于24个项目的完整信息,包括对7种变应原的皮肤试验反应、血清总IgE水平、是否有哮喘发作、喘息发作、花粉症和咳嗽。然后将因子得分系数应用于所有同胞(n = 877),得出定量因子得分。进行单点和多点非参数同胞对分析,以评估与5号染色体q31 - 33上标记的连锁。也对单个项目进行了分析。

结果

确定了两个主要因子:因子I在特应性项目上有高负荷,包括皮肤试验反应、IgE和花粉症,因子II在包括哮喘诊断、喘息、咳嗽和链格孢属皮肤试验反应等项目上有高负荷。因子I和因子II的相关系数r值为0.19。对于定量因子得分,仅在特应性因子I上显示出显著的单点连锁(P <.0001),并且在标记D5S479处观察到峰值多点LOD得分为2.7。单个项目的多点LOD得分均为1.1或更低。

结论

这些分析表明存在一个或多个定位于5号染色体q31 - 33的基因座,与这种复合特应性表型相关。

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