Genome-wide search for atopy susceptibility genes in Dutch families with asthma

被引:142
作者
Koppelman, GH
Stine, OC
Xu, JF
Howard, TD
Zheng, SQL
Kauffman, HF
Bleecker, ER
Meyers, DA
Postma, DS
机构
[1] Beatrixoord, Dept Pulm Rehabil, Haren, Netherlands
[2] Univ Groningen Hosp, Dept Pulmonol, Groningen, Netherlands
[3] Univ Groningen Hosp, Dept Allergol, Groningen, Netherlands
[4] Univ Maryland, Sch Med, Dept Epidemiol & Prevent Med, Baltimore, MD 21201 USA
[5] Wake Forest Univ, Sch Med, Ctr Human Genomics, Winston Salem, NC 27109 USA
关键词
genetics of atopy; asthma; specific IgE; eosinophils; genoine-wide search;
D O I
10.1067/mai.2002.122235
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Atopy is a phenotype associated with asthma that has a heritable component. However, the role of atopy-susceptibility genes in the development and expression of asthma and allergic disorders is not understood. Objective: We sought to study the familial aggregation and co-occurrence of atopic phenotypes within family members of patients with asthma and to identify chromosomal regions that may contain genes that regulate different atopic phenotypes. Methods: In 200 families (n = 1174) ascertained through a proband with asthma, genome-wide screen and linkage analysis was performed for the following atopic phenotypes: (1) specific IgE to common aeroallergens (Phadiatop assay); (2) specific IgE to Der p 1; (3) positive skin test responses to house dust mite; (4) positive skin test responses to 1 or more of 16 allergens; and (5) peripheral blood eosinophils. Results were compared with the linkage results for total serum IgE levels. Results: There was clear familial aggregation of atopy. A high total serum IgE level in combination with a positive Phadiatop result or a normal total IgE level in combination with a negative Phadiatop result was found in 56.1% of the probands and 66.9% of the offspring. Several chromosomal regions that showed evidence for linkage to an atopic phenotype (ie, 2q, 6p, 7q, and 13q) also showed evidence of linkage with total serum IgE (Xu et al. Am J Hum Genet 2000;67:1163-73). Specific regions of interest for atopic traits were also detected on chromosomes 11q, 17q, and 22q. Conclusions: Atopic phenotypes show familial aggregation, although family members may differ in expression of atopy. Specific chromosomal regions appear to be important in susceptibility to different phenotypes of atopic responsiveness.
引用
收藏
页码:498 / 506
页数:9
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