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本文引用的文献

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Discovery of rare variants via sequencing: implications for the design of complex trait association studies.通过测序发现罕见变异:对复杂性状关联研究设计的启示
PLoS Genet. 2009 May;5(5):e1000481. doi: 10.1371/journal.pgen.1000481. Epub 2009 May 15.
2
Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene.全基因组关联分析确定磷酸二酯酶4D(PDE4D)为哮喘易感基因。
Am J Hum Genet. 2009 May;84(5):581-93. doi: 10.1016/j.ajhg.2009.04.006. Epub 2009 May 7.
3
The genetic structure and history of Africans and African Americans.非洲人和非裔美国人的基因结构与历史。
Science. 2009 May 22;324(5930):1035-44. doi: 10.1126/science.1172257. Epub 2009 Apr 30.
4
ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry.与欧洲裔北美人群哮喘易感性相关的ORMDL3变异体。
J Allergy Clin Immunol. 2008 Dec;122(6):1225-7. doi: 10.1016/j.jaci.2008.06.041. Epub 2008 Aug 28.
5
Common and rare variants in multifactorial susceptibility to common diseases.常见疾病多因素易感性中的常见和罕见变异。
Nat Genet. 2008 Jun;40(6):695-701. doi: 10.1038/ng.f.136.
6
The cellular prion protein is preferentially expressed by CD4+ CD25+ Foxp3+ regulatory T cells.细胞朊蛋白优先由CD4 + CD25 + Foxp3 +调节性T细胞表达。
Immunology. 2008 Nov;125(3):313-9. doi: 10.1111/j.1365-2567.2008.02853.x. Epub 2008 May 6.
7
Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function.几丁质酶3样蛋白1(CHI3L1)的变异对血清YKL-40水平、哮喘风险和肺功能的影响。
N Engl J Med. 2008 Apr 17;358(16):1682-91. doi: 10.1056/NEJMoa0708801. Epub 2008 Apr 9.
8
How to interpret a genome-wide association study.如何解读全基因组关联研究。
JAMA. 2008 Mar 19;299(11):1335-44. doi: 10.1001/jama.299.11.1335.
9
ORMDL3 gene is associated with asthma in three ethnically diverse populations.ORMDL3基因在三个不同种族群体中与哮喘相关。
Am J Respir Crit Care Med. 2008 Jun 1;177(11):1194-200. doi: 10.1164/rccm.200711-1644OC. Epub 2008 Feb 28.
10
Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms.关联研究模式的转变:罕见单核苷酸多态性的价值
Am J Hum Genet. 2008 Jan;82(1):100-12. doi: 10.1016/j.ajhg.2007.09.006.

一项针对非洲裔人群哮喘的全基因组关联研究。

A genome-wide association study on African-ancestry populations for asthma.

机构信息

Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA.

出版信息

J Allergy Clin Immunol. 2010 Feb;125(2):336-346.e4. doi: 10.1016/j.jaci.2009.08.031. Epub 2009 Nov 11.

DOI:10.1016/j.jaci.2009.08.031
PMID:19910028
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3606015/
Abstract

BACKGROUND

Asthma is a complex disease characterized by striking ethnic disparities not explained entirely by environmental, social, cultural, or economic factors. Of the limited genetic studies performed on populations of African descent, notable differences in susceptibility allele frequencies have been observed.

OBJECTIVES

We sought to test the hypothesis that some genes might contribute to the profound disparities in asthma.

METHODS

We performed a genome-wide association study in 2 independent populations of African ancestry (935 African American asthmatic cases and control subjects from the Baltimore-Washington, DC, area and 929 African Caribbean asthmatic subjects and their family members from Barbados) to identify single-nucleotide polymorphisms (SNPs) associated with asthma.

RESULTS

A meta-analysis combining these 2 African-ancestry populations yielded 3 SNPs with a combined P value of less than 10(-5) in genes of potential biologic relevance to asthma and allergic disease: rs10515807, mapping to the alpha-1B-adrenergic receptor (ADRA1B) gene on chromosome 5q33 (3.57 x 10(-6)); rs6052761, mapping to the prion-related protein (PRNP) gene on chromosome 20pter-p12 (2.27 x 10(-6)); and rs1435879, mapping to the dipeptidyl peptidase 10 (DPP10) gene on chromosome 2q12.3-q14.2. The generalizability of these findings was tested in family and case-control panels of United Kingdom and German origin, respectively, but none of the associations observed in the African groups were replicated in these European studies. Evidence for association was also examined in 4 additional case-control studies of African Americans; however, none of the SNPs implicated in the discovery population were replicated.

CONCLUSIONS

This study illustrates the complexity of identifying true associations for a complex and heterogeneous disease, such as asthma, in admixed populations, especially populations of African descent.

摘要

背景

哮喘是一种复杂的疾病,其显著的种族差异不能完全用环境、社会、文化或经济因素来解释。在对非洲裔人群进行的有限的遗传研究中,已经观察到易感等位基因频率的显著差异。

目的

我们试图检验某些基因可能导致哮喘严重种族差异的假设。

方法

我们对两个具有非洲血统的独立人群(来自巴尔的摩-华盛顿特区地区的 935 名非裔美国哮喘病例和对照以及来自巴巴多斯的 929 名非裔加勒比哮喘患者及其家庭成员)进行了全基因组关联研究,以鉴定与哮喘相关的单核苷酸多态性(SNP)。

结果

对这两个非洲血统人群进行的荟萃分析产生了 3 个 SNP,它们在与哮喘和过敏性疾病具有潜在生物学相关性的基因中具有小于 10(-5)的联合 P 值:rs10515807,位于染色体 5q33 的α-1B-肾上腺素能受体(ADRA1B)基因上(3.57 x 10(-6)); rs6052761,位于染色体 20pter-p12 上的朊病毒相关蛋白(PRNP)基因上(2.27 x 10(-6)); 和 rs1435879,位于染色体 2q12.3-q14.2 上的二肽基肽酶 10(DPP10)基因上。这些发现的可推广性分别在英国和德国的家系和病例对照面板中进行了测试,但在这些欧洲研究中,没有一个在非洲人群中观察到的关联得到复制。在另外 4 项非裔美国人的病例对照研究中也对关联进行了检验;然而,在发现人群中涉及的 SNP 均未得到复制。

结论

这项研究说明了在混合人群中识别复杂和异质疾病(如哮喘)的真正关联的复杂性,尤其是非洲裔人群。