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5号染色体和11号染色体上基因标记与特应性和支气管高反应性的等位基因关联。

Allelic association of gene markers on chromosomes 5q and 11q with atopy and bronchial hyperresponsiveness.

作者信息

Doull I J, Lawrence S, Watson M, Begishvili T, Beasley R W, Lampe F, Holgate T, Morton N E

机构信息

Genetic Epidemiology, University Medicine, University of Southampton, Southampton General Hospital, United Kingdom.

出版信息

Am J Respir Crit Care Med. 1996 Apr;153(4 Pt 1):1280-4. doi: 10.1164/ajrccm.153.4.8616554.

DOI:10.1164/ajrccm.153.4.8616554
PMID:8616554
Abstract

To investigate genetic factors in asthma and atopy, we sought allelic associations for 12 markers near candidate loci for serum total, immunoglobulin E (IgE), and bronchial hyperresponsiveness (BHR) to inhaled histamine in 131 families comprising 685 individuals, selected randomly without regard to atopy or asthma. Nonparametric linkage and association analyses were performed with the Nonparametric Analysis of Lineage and Association (NOPAR) program, and parametric analyses were performed with the Complex Inheritance with Diathesis and Severity (COMDS) program on an ordered polychotomy of ranked scores. On chromosome 11q, allele 168 at the D11S527 locus was significantly associated with BHR (p<0.0003) but not with log IgE. At the D11S534 locus, allele 235 was significantly associated with log IgE (p = 0.007) but not with BHR. Both D11S527 and D11S534 were too distant from the gene encoding the high-affinity IgE receptor FcepsilonRIbeta to account for the association. At the interleukin-9 (IL-9) locus, the 118 allele showed significant association with serum total IgE (p<0.003) but not with histamine BHR. Parametric tests are more conservative, perhaps because they demand consistency with mendelian inheritance and tight linkage. These findings provide support for the view that both chromosomes 5 and 11 may contain genes relevant to asthma and atopy, a possible candidate being the interleukin-4 (IL-4) gene cluster. Because these associations are extremes in a large number of tests, they require confirmation in other samples.

摘要

为了研究哮喘和特应性疾病中的遗传因素,我们在131个家庭(共685人)中,对血清总免疫球蛋白E(IgE)以及对吸入组胺的支气管高反应性(BHR)候选基因座附近的12个标记进行等位基因关联研究,这些家庭是随机选取的,不考虑是否患有特应性疾病或哮喘。使用谱系和关联非参数分析(NOPAR)程序进行非参数连锁和关联分析,并使用易感性和严重性复杂遗传(COMDS)程序对排序分数的有序多分类进行参数分析。在11号染色体上,D11S527基因座的168等位基因与BHR显著相关(p<0.0003),但与IgE对数无关。在D11S534基因座,235等位基因与IgE对数显著相关(p = 0.007),但与BHR无关。D11S527和D11S534与编码高亲和力IgE受体FcepsilonRIbeta的基因距离都太远,无法解释这种关联。在白细胞介素-9(IL-9)基因座,118等位基因与血清总IgE显著相关(p<0.003),但与组胺BHR无关。参数检验更为保守,可能是因为它们要求与孟德尔遗传和紧密连锁保持一致。这些发现支持了这样一种观点,即5号和11号染色体可能都包含与哮喘和特应性疾病相关的基因,白细胞介素-4(IL-4)基因簇可能是一个候选基因。由于这些关联是大量检验中的极端情况,需要在其他样本中进行验证。

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