Puthothu Beena, Forster Johannes, Heinze Jessica, Heinzmann Andrea, Krueger Marcus
University Children's Hospital, University of Freiburg, Freiburg, Germany.
BMC Pulm Med. 2007 May 11;7:6. doi: 10.1186/1471-2466-7-6.
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.
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.
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).
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.
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。
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。
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)。
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。