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Absence of genetic linkage of chromosome 5q31 with asthma and atopy in the general population

机译:普通人群中没有5q31染色体与哮喘和特应性遗传联系

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摘要

BACKGROUND: Clinical asthma is associated with increased serum total immunoglobulin E (IgE), atopy (skin prick test positivity to common aeroallergens), and bronchial hyperreactivity (BHR) to non-specific stimuli (positive methacholine challenge test). A region on chromosome 5q31-33 has been linked with increased total serum IgE and BHR. A study of the genetic linkage of this region with clinical asthma and atopy was therefore undertaken. METHODS: A polymorphic microsatellite marker in chromosome 5q31 (D5S399) was studied in 119 sibling pairs recruited from the general population who shared asthma, atopy, and/or BHR. Based on our population distribution of 13 different alleles, it was expected that by chance alone sibling pairs would share on average 1.24 alleles and that a significant excess would indicate genetic linkage. RESULTS: No evidence of linkage was found in 45 siblings concordant for asthma (shared alleles = 1.09, p = 0.95), in 103 sibling pairs with atopy (shared alleles = 1.18, p = 0.82), in 51 sibling pairs with BHR (shared alleles = 1.22, p = 0.62), or in 68 sibling pairs who shared atopy in the absence of BHR (shared alleles = 1.22, p = 0.61). A slight non- significant excess of shared alleles (1.44, p = 0.11) was observed in siblings who shared BHR without atopy. CONCLUSIONS: No evidence of genetic linkage of chromosome 5q31 with either clinical asthma or atopy was therefore detected in the population studied. Linkage between chromosome 5q and BHR needs further investigation.


机译:背景:临床哮喘与血清总免疫球蛋白E(IgE)升高,特应性(对普通气变应原的皮刺试验阳性)和对非特异性刺激的支气管高反应性(BHR)(阳性乙酰甲胆碱激发试验)相关。染色体5q31-33上的一个区域与总血清IgE和BHR升高有关。因此,对该区域与临床哮喘和特应性的遗传联系进行了研究。方法:在从患有哮喘,特应性和/或BHR的普通人群中招募的119对兄弟姐妹中研究了5q31染色体上的多态性微卫星标记(D5S399)。根据我们的13种不同等位基因的种群分布,可以预期,仅偶然的兄弟姐妹对将平均共享1.24个等位基因,并且显着过量将表明遗传连锁。结果:在与哮喘相符的45个兄弟姐妹中(共享等位基因= 1.09,p = 0.95),在特应性的103个兄弟姐妹对中(共享的等位基因= 1.18,p = 0.82),在与BHR的51个兄弟姐妹对中(共享)没有发现关联的证据。等位基因= 1.22,p = 0.62),或在没有BHR的情况下有特应性的68对同胞对(共享等位基因= 1.22,p = 0.61)。在没有特应性的情况下,共享BHR的兄弟姐妹中观察到的共享等位基因略有非显着过量(1.44,p = 0.11)。结论:因此没有在研究人群中发现5q31染色体与临床哮喘或特应性遗传相关的证据。 5q染色体与BHR之间的联系需要进一步研究。


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