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本文引用的文献

1
Identification of FGF7 as a novel susceptibility locus for chronic obstructive pulmonary disease.鉴定 FGF7 为慢性阻塞性肺疾病的一个新的易感基因位点。
Thorax. 2011 Dec;66(12):1085-90. doi: 10.1136/thoraxjnl-2011-200017. Epub 2011 Sep 15.
2
Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.全基因组关联研究鉴定出与甲状腺体积和甲状腺肿风险相关的四个遗传位点。
Am J Hum Genet. 2011 May 13;88(5):664-73. doi: 10.1016/j.ajhg.2011.04.015.
3
Keratinocyte growth factor gene transduction ameliorates pulmonary fibrosis induced by bleomycin in mice.角质细胞生长因子基因转导改善博莱霉素诱导的小鼠肺纤维化。
Am J Respir Cell Mol Biol. 2011 Sep;45(3):489-97. doi: 10.1165/rcmb.2010-0092OC. Epub 2010 Dec 3.
4
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.
5
The COPD genetic association compendium: a comprehensive online database of COPD genetic associations.COPD 遗传关联综合数据库:一个 COPD 遗传关联的综合在线数据库。
Hum Mol Genet. 2010 Feb 1;19(3):526-34. doi: 10.1093/hmg/ddp519. Epub 2009 Nov 20.
6
A genome-wide association study of pulmonary function measures in the Framingham Heart Study.弗雷明汉心脏研究中肺功能指标的全基因组关联研究。
PLoS Genet. 2009 Mar;5(3):e1000429. doi: 10.1371/journal.pgen.1000429. Epub 2009 Mar 20.
7
A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci.一项慢性阻塞性肺疾病(COPD)的全基因组关联研究:两个主要易感基因座的鉴定。
PLoS Genet. 2009 Mar;5(3):e1000421. doi: 10.1371/journal.pgen.1000421. Epub 2009 Mar 20.
8
Prevalence of chronic obstructive pulmonary disease in China: a large, population-based survey.中国慢性阻塞性肺疾病的患病率:一项基于人群的大型调查。
Am J Respir Crit Care Med. 2007 Oct 15;176(8):753-60. doi: 10.1164/rccm.200612-1749OC. Epub 2007 Jun 15.
9
Impaired FGF signaling contributes to cleft lip and palate.成纤维细胞生长因子(FGF)信号传导受损会导致唇腭裂。
Proc Natl Acad Sci U S A. 2007 Mar 13;104(11):4512-7. doi: 10.1073/pnas.0607956104. Epub 2007 Mar 6.
10
Keratinocyte growth factor gene transduction ameliorates acute lung injury and mortality in mice.角质形成细胞生长因子基因转导可改善小鼠急性肺损伤并降低死亡率。
Hum Gene Ther. 2007 Feb;18(2):130-41. doi: 10.1089/hum.2006.137.

成纤维细胞生长因子7与慢性阻塞性肺疾病风险之间的关联。

Association between fibroblast growth factor 7 and the risk of chronic obstructive pulmonary disease.

作者信息

Xu Si-cheng, Kuang Jiang-ying, Liu Jin, Ma Chun-lan, Feng Yu-lin, Su Zhi-guang

机构信息

Molecular Medicine Research Center, West China Hospital, and State Key Laboratory of Biotherapy, Sichuan University, Chengdu 610041, China.

出版信息

Acta Pharmacol Sin. 2012 Aug;33(8):998-1003. doi: 10.1038/aps.2012.69. Epub 2012 Jul 16.

DOI:10.1038/aps.2012.69
PMID:22796760
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4011325/
Abstract

AIM

Fibroblast growth factor 7 (FGF7) is involved in a number of physiological and pathological processes, including lung disease. However, relatively little is known about the effect of FGF7 gene polymorphisms on chronic obstructive pulmonary disease (COPD) susceptibility. This study aimed to investigate the association between FGF7 polymorphisms with COPD susceptibility in a Chinese Han population.

METHODS

We conducted a case-control study of 279 COPD patients and 367 age- and gender-distribution-matched control subjects. The tagging SNPs rs10519225 and rs7170426 in FGF7 were genotyped by SNaPshot. The associations of each SNP genotype and haplotype constructed by these loci with COPD were analyzed.

RESULTS

A multivariate analysis showed that rs10519225 was significantly associated with an increased risk of COPD (P=0.011, OR=1.535, FDR q=0.022), whereas no association was found for rs7170426. Linkage disequilibrium (LD) analysis showed that these loci were in weak LD, with an r(2) of 0.033 and a D' of 0.232 (95% CI: 0.150-0.520). The haplotype constructed by allele G at rs10519225 and allele A at rs7170426 was associated with a decreased susceptibility to COPD (P=0.012, OR=0.751, FDR q=0.048).

CONCLUSION

These findings suggest that FGF7 may be one susceptibility factor for COPD.

摘要

目的

成纤维细胞生长因子7(FGF7)参与包括肺部疾病在内的多种生理和病理过程。然而,关于FGF7基因多态性对慢性阻塞性肺疾病(COPD)易感性的影响,人们了解相对较少。本研究旨在探讨中国汉族人群中FGF7基因多态性与COPD易感性之间的关联。

方法

我们对279例COPD患者和367例年龄及性别分布匹配的对照者进行了病例对照研究。通过SNaPshot对FGF7中的标签单核苷酸多态性(SNP)rs10519225和rs7170426进行基因分型。分析了每个SNP基因型以及由这些位点构建的单倍型与COPD的关联。

结果

多因素分析显示,rs10519225与COPD风险增加显著相关(P = 0.011,比值比[OR]=1.535,错误发现率[FDR] q = 0.022),而rs7170426未发现关联。连锁不平衡(LD)分析表明,这些位点处于弱LD状态,r²为0.033,D'为0.232(95%置信区间:0.150 - 0.520)。由rs10519225处的等位基因G和rs7170426处的等位基因A构建的单倍型与COPD易感性降低相关(P = 0.012,OR = 0.751,FDR q = 0.048)。

结论

这些发现提示FGF7可能是COPD的一个易感因素。