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拉丁裔人群的病例-对照混合映射方法富集了已知与哮喘相关的基因。

Case-control admixture mapping in Latino populations enriches for known asthma-associated genes.

机构信息

Department of Medicine, University of California San Francisco, San Francisco, CA 94158, USA.

出版信息

J Allergy Clin Immunol. 2012 Jul;130(1):76-82.e12. doi: 10.1016/j.jaci.2012.02.040. Epub 2012 Apr 13.

Abstract

BACKGROUND

Polymorphisms in more than 100 genes have been associated with asthma susceptibility, yet much of the heritability remains to be explained. Asthma disproportionately affects different racial and ethnic groups in the United States, suggesting that admixture mapping is a useful strategy to identify novel asthma-associated loci.

OBJECTIVE

We sought to identify novel asthma-associated loci in Latino populations using case-control admixture mapping.

METHODS

We performed genome-wide admixture mapping by comparing levels of local Native American, European, and African ancestry between children with asthma and nonasthmatic control subjects in Puerto Rican and Mexican populations. Within candidate peaks, we performed allelic tests of association, controlling for differences in local ancestry.

RESULTS

Between the 2 populations, we identified a total of 62 admixture mapping peaks at a P value of less than 10(-3) that were significantly enriched for previously identified asthma-associated genes (P= .0051). One of the peaks was statistically significant based on 100 permutations in the Mexican sample (6q15); however, it was not significant in Puerto Rican subjects. Another peak was identified at nominal significance in both populations (8q12); however, the association was observed with different ancestries.

CONCLUSION

Case-control admixture mapping is a promising strategy for identifying novel asthma-associated loci in Latino populations and implicates genetic variation at 6q15 and 8q12 regions with asthma susceptibility. This approach might be useful for identifying regions that contribute to both shared and population-specific differences in asthma susceptibility.

摘要

背景

已有超过 100 个基因的多态性与哮喘易感性相关,但仍有很大一部分遗传率尚未得到解释。哮喘在美国不同种族和族裔群体中的发病率不成比例,这表明混合映射是一种识别新的哮喘相关基因座的有用策略。

目的

我们试图通过病例对照混合映射来确定拉丁裔人群中的新的哮喘相关基因座。

方法

我们通过比较波多黎各和墨西哥人群中哮喘儿童和非哮喘对照个体之间的本地美洲原住民、欧洲和非洲血统水平,进行了全基因组混合映射。在候选峰内,我们进行了等位基因关联的测试,控制了本地血统的差异。

结果

在这两个群体中,我们总共鉴定出 62 个混合映射峰,其 P 值小于 10(-3),这些峰显著富集了先前鉴定出的与哮喘相关的基因(P=.0051)。一个峰在墨西哥样本的 100 次随机排列中具有统计学意义(6q15);然而,在波多黎各人群中并不显著。另一个峰在两个群体中均达到了名义上的显著性(8q12);然而,这种关联与不同的血统有关。

结论

病例对照混合映射是一种在拉丁裔人群中识别新的哮喘相关基因座的有前途的策略,该方法提示 6q15 和 8q12 区域的遗传变异与哮喘易感性有关。这种方法可能有助于识别导致哮喘易感性共享和特定人群差异的区域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32f9/3593143/729b748e1893/nihms-361987-f0001.jpg

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