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Association of surfactant protein B gene polymorphisms (C/A-18, C/T1580, intron 4 and A/G9306) and haplotypes with bronchopulmonary dysplasia in chinese han population.中国汉族人群中表面活性蛋白B基因多态性(C/A-18、C/T1580、内含子4和A/G9306)及单倍型与支气管肺发育不良的相关性
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本文引用的文献

1
Haplotypes of surfactant protein C are associated with common paediatric lung diseases.表面活性蛋白C的单倍型与常见儿科肺部疾病相关。
Pediatr Allergy Immunol. 2006 Dec;17(8):572-7. doi: 10.1111/j.1399-3038.2006.00467.x.
2
Surfactant protein levels in bronchoalveolar lavage after segmental allergen challenge in patients with asthma.哮喘患者节段性变应原激发后支气管肺泡灌洗中的表面活性物质蛋白水平。
Allergy. 2006 May;61(5):598-604. doi: 10.1111/j.1398-9995.2006.01062.x.
3
Severe respiratory syncytial virus bronchiolitis in infancy and asthma and allergy at age 13.婴儿期严重呼吸道合胞病毒细支气管炎与13岁时的哮喘和过敏
Am J Respir Crit Care Med. 2005 Jan 15;171(2):137-41. doi: 10.1164/rccm.200406-730OC. Epub 2004 Oct 29.
4
Prospective population-based study of viral lower respiratory tract infections in children under 3 years of age (the PRI.DE study).3岁以下儿童病毒性下呼吸道感染的前瞻性人群研究(PRI.DE研究)
Eur J Pediatr. 2004 Dec;163(12):709-16. doi: 10.1007/s00431-004-1523-9.
5
Maximum-likelihood estimation of haplotype frequencies in nuclear families.核心家庭中单体型频率的最大似然估计。
Genet Epidemiol. 2004 Jul;27(1):21-32. doi: 10.1002/gepi.10323.
6
Association study of the IL13 variant Arg110Gln in atopic diseases and juvenile idiopathic arthritis.
J Allergy Clin Immunol. 2003 Oct;112(4):735-9. doi: 10.1016/s0091-6749(03)01887-6.
7
Surfactant protein B intron 4 variation in German patients with COPD and acute respiratory failure.德国慢性阻塞性肺疾病(COPD)和急性呼吸衰竭患者的表面活性蛋白B内含子4变异
Dis Markers. 2002;18(3):129-36. doi: 10.1155/2002/194075.
8
Faster haplotype frequency estimation using unrelated subjects.利用无关个体更快地估计单倍型频率。
Hum Hered. 2002;53(1):36-41. doi: 10.1159/000048602.
9
Surfactant protein (SP) B associations and interactions with SP-A in white and black subjects with respiratory distress syndrome.患有呼吸窘迫综合征的白种人和黑种人中表面活性物质蛋白(SP)B与SP - A的关联及相互作用。
Pediatr Int. 2001 Dec;43(6):567-76. doi: 10.1046/j.1442-200x.2001.01474.x.
10
Surfactant regulation of host defense function in the lung: a question of balance.肺中表面活性剂对宿主防御功能的调节:平衡问题。
Pediatr Pathol Mol Med. 2001 Jul-Aug;20(4):269-92.

表面活性蛋白B基因多态性与严重呼吸道合胞病毒感染相关,但与哮喘无关。

Surfactant protein B polymorphisms are associated with severe respiratory syncytial virus infection, but not with asthma.

作者信息

Puthothu Beena, Forster Johannes, Heinze Jessica, Heinzmann Andrea, Krueger Marcus

机构信息

University Children's Hospital, University of Freiburg, Freiburg, Germany.

出版信息

BMC Pulm Med. 2007 May 11;7:6. doi: 10.1186/1471-2466-7-6.

DOI:10.1186/1471-2466-7-6
PMID:17498296
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1877814/
Abstract

BACKGROUND

Surfactant proteins (SP) are important for the innate host defence and essential for a physiological lung function. Several linkage and association studies have investigated the genes coding for different surfactant proteins in the context of pulmonary diseases such as chronic obstructive pulmonary disease or respiratory distress syndrome of preterm infants. In this study we tested whether SP-B was in association with two further pulmonary diseases in children, i. e. severe infections caused by respiratory syncytial virus and bronchial asthma.

METHODS

We chose to study five polymorphisms in SP-B: rs2077079 in the promoter region; rs1130866 leading to the amino acid exchange T131I; rs2040349 in intron 8; rs3024801 leading to L176F and rs3024809 resulting in R272H. Statistical analyses made use of the Armitage's trend test for single polymorphisms and FAMHAP and FASTEHPLUS for haplotype analyses.

RESULTS

The polymorphisms rs3024801 and rs3024809 were not present in our study populations. The three other polymorphisms were common and in tight linkage disequilibrium with each other. They did not show association with bronchial asthma or severe RSV infection in the analyses of single polymorphisms. However, haplotypes analyses revealed association of SP-B with severe RSV infection (p = 0.034).

CONCLUSION

Thus our results indicate a possible involvement of SP-B in the genetic predisposition to severe RSV infections in the German population. In order to determine which of the three polymorphisms constituting the haplotypes is responsible for the association, further case control studies on large populations are necessary. Furthermore, functional analysis need to be conducted.

摘要

背景

表面活性物质蛋白(SP)对宿主天然防御至关重要,对肺的生理功能必不可少。多项连锁和关联研究在慢性阻塞性肺疾病或早产儿呼吸窘迫综合征等肺部疾病背景下,对编码不同表面活性物质蛋白的基因进行了研究。在本研究中,我们测试了SP-B是否与儿童的另外两种肺部疾病相关,即呼吸道合胞病毒引起的严重感染和支气管哮喘。

方法

我们选择研究SP-B中的五个多态性:启动子区域的rs2077079;导致氨基酸交换T131I的rs1130866;内含子8中的rs2040349;导致L176F的rs3024801和导致R272H的rs3024809。统计分析使用针对单个多态性的阿米蒂奇趋势检验以及用于单倍型分析的FAMHAP和FASTEHPLUS。

结果

多态性rs3024801和rs3024809在我们的研究人群中不存在。其他三个多态性很常见且彼此处于紧密连锁不平衡状态。在单个多态性分析中,它们未显示与支气管哮喘或严重呼吸道合胞病毒感染相关。然而,单倍型分析显示SP-B与严重呼吸道合胞病毒感染相关(p = 0.034)。

结论

因此,我们的结果表明SP-B可能参与德国人群中严重呼吸道合胞病毒感染的遗传易感性。为了确定构成单倍型的三个多态性中的哪一个与该关联有关,有必要对大量人群进行进一步的病例对照研究。此外,需要进行功能分析。