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Variants in FAM13A are associated with chronic obstructive pulmonary disease.FAM13A 中的变异与慢性阻塞性肺疾病有关。
Nat Genet. 2010 Mar;42(3):200-2. doi: 10.1038/ng.535. Epub 2010 Feb 21.
2
Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions.全基因组关联研究哮喘确定 RAD50-IL13 和 HLA-DR/DQ 区域。
J Allergy Clin Immunol. 2010 Feb;125(2):328-335.e11. doi: 10.1016/j.jaci.2009.11.018.
3
Lung function and airway diseases.肺功能和气道疾病。
Nat Genet. 2010 Jan;42(1):14-6. doi: 10.1038/ng0110-14.
4
Variants of DENND1B associated with asthma in children.与儿童哮喘相关的 DENND1B 变异体。
N Engl J Med. 2010 Jan 7;362(1):36-44. doi: 10.1056/NEJMoa0901867. Epub 2009 Dec 23.
5
MMP12, lung function, and COPD in high-risk populations.MMP12、肺功能与高危人群的 COPD。
N Engl J Med. 2009 Dec 31;361(27):2599-608. doi: 10.1056/NEJMoa0904006. Epub 2009 Dec 16.
6
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.全基因组关联研究的荟萃分析确定了多个与肺功能相关的基因座。
Nat Genet. 2010 Jan;42(1):45-52. doi: 10.1038/ng.500. Epub 2009 Dec 13.
7
Genome-wide association study identifies five loci associated with lung function.全基因组关联研究鉴定出与肺功能相关的五个位点。
Nat Genet. 2010 Jan;42(1):36-44. doi: 10.1038/ng.501. Epub 2009 Dec 13.
8
A genome-wide association study on African-ancestry populations for asthma.一项针对非洲裔人群哮喘的全基因组关联研究。
J Allergy Clin Immunol. 2010 Feb;125(2):336-346.e4. doi: 10.1016/j.jaci.2009.08.031. Epub 2009 Nov 11.
9
Identification of asthma phenotypes using cluster analysis in the Severe Asthma Research Program.利用严重哮喘研究计划中的聚类分析鉴定哮喘表型。
Am J Respir Crit Care Med. 2010 Feb 15;181(4):315-23. doi: 10.1164/rccm.200906-0896OC. Epub 2009 Nov 5.
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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.

hedgehog 相互作用蛋白及其他肺功能基因在哮喘中的重要性。

Importance of hedgehog interacting protein and other lung function genes in asthma.

机构信息

Center for Genomics and Personalized Medicine Research, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.

出版信息

J Allergy Clin Immunol. 2011 Jun;127(6):1457-65. doi: 10.1016/j.jaci.2011.01.056. Epub 2011 Mar 12.

DOI:10.1016/j.jaci.2011.01.056
PMID:21397937
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3105202/
Abstract

BACKGROUND

Two recent large meta-analyses of genome-wide association studies of lung function in general populations of European descent identified 11 candidate genes/regions. The importance of these genes in lung function in white and African American subjects with asthma is unknown.

OBJECTIVES

To determine whether genes that regulate lung function in general populations are associated with lung function abnormalities in subjects with asthma from different racial groups.

METHODS

Single nucleotide polymorphisms (SNPs) were tested in 5 asthma populations (N = 1441) for association with pulmonary function, and meta-analysis was performed across populations. The SNPs with the highest significance were then tested for association with bronchodilator reversibility and bronchial hyperresponsiveness to methacholine. A joint analysis of consistently replicated SNPs was performed to predict lung function in asthma.

RESULTS

Hedgehog interacting protein (HHIP) on chromosome 4q31 was associated with lung function in all 5 populations (rs1512288: P(meta) = 9.62E-05 and 3.23E-05 for percent predicted FEV(1) [ppFEV(1)] and percent predicted forced vital capacity [ppFVC], respectively). The SNPs in HHIP were also associated with reversibility (P < .05) but not bronchial hyperresponsiveness to methacholine. Because of differences in linkage disequilibrium in the African American subjects, the most relevant SNPs in HHIP were identified. A subset of normal lung function genes, including HHIP, family with sequence similarity 13, member A (FAM13A), and patched homolog 1 (PTCH1), together predict lung function abnormalities, a measure of severity in white and African American subjects with asthma.

CONCLUSION

A subset of the genes, including HHIP, that regulate lung function in general populations are associated with abnormal lung function in asthma in non-Hispanic white and African American subjects.

摘要

背景

最近两项针对欧洲血统普通人群肺功能的全基因组关联研究的荟萃分析确定了 11 个候选基因/区域。这些基因在白人和非裔美国人哮喘患者的肺功能中的重要性尚不清楚。

目的

确定在不同种族的哮喘患者中,调节普通人群肺功能的基因是否与肺功能异常相关。

方法

对 5 个哮喘人群(N=1441)中的单核苷酸多态性(SNP)进行检测,以评估其与肺功能的相关性,并在人群间进行荟萃分析。然后,对具有最高显著性的 SNP 进行支气管扩张剂可逆性和乙酰甲胆碱支气管高反应性的相关性检测。对一致复制的 SNP 进行联合分析,以预测哮喘患者的肺功能。

结果

4q31 上的 Hedgehog 相互作用蛋白(HHIP)与所有 5 个人群的肺功能相关(rs1512288:预测 FEV1 百分比[ppFEV1]和预测用力肺活量百分比[ppFVC]的全人群荟萃分析 P 值分别为 9.62E-05 和 3.23E-05)。HHIP 中的 SNP 也与可逆性相关(P<0.05),但与乙酰甲胆碱支气管高反应性无关。由于非裔美国人的连锁不平衡存在差异,因此确定了与 HHIP 最相关的 SNP。HHIP、家族性序列相似性 13 成员 A(FAM13A)和 patched 同源物 1(PTCH1)等正常肺功能基因的一个子集,共同预测了白人和非裔美国人哮喘患者的肺功能异常,这是严重程度的一个衡量标准。

结论

包括 HHIP 在内的一组基因,在普通人群中调节肺功能,与非西班牙裔白人和非裔美国人哮喘患者的肺功能异常相关。