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表面活性蛋白基因A和D的单倍型作为呼吸窘迫综合征发生发展的易感因素。

Haplotypes of the surfactant protein genes A and D as susceptibility factors for the development of respiratory distress syndrome.

作者信息

Thomas Neal J, Fan Ruzong, Diangelo Susan, Hess Joseph C, Floros Joanna

机构信息

Department of Pediatrics, Penn State Children's Hospita, Pennsylvania State University College of Medicine, Hershey, Pennsylvania 17033, USA.

出版信息

Acta Paediatr. 2007 Jul;96(7):985-9. doi: 10.1111/j.1651-2227.2007.00319.x. Epub 2007 May 24.

Abstract

AIMS

Polymorphisms of genes are transmitted together in haplotypes, which can be used in the study of the development of complex diseases such as respiratory distress syndrome (RDS). The surfactant proteins (SPs) play important roles in lung function, and genetic variants of these proteins have been linked with lung diseases, including RDS. To determine whether haplotypes of SP-A and SP-D are transmitted disproportionately from parents to offspring with RDS, we hypothesized that previously unstudied genetic haplotypes of these SP genes are associated with the development of RDS.

METHODS

DNA was collected from 132 families of neonates with RDS. Genotyping was performed, and haplotype transmission from parent to offspring was determined by transmission disequilibrium test.

RESULTS

The two-marker SP-D/SP-A haplotype DA160_A/SP-A2 1A(1) is protective against the development of RDS (p = 0.035). Four three- and four-marker haplotypes containing one or both loci from the significant two-marker haplotype are also protective against the development of RDS.

CONCLUSIONS

These data identify protective haplotypes against RDS and support findings related to SP genetic differences in children who develop RDS. Study of haplotypes in complex diseases with both genetic and environmental risk factors may lead to better understanding of these types of diseases.

摘要

目的

基因多态性以单倍型形式共同传递,可用于研究诸如呼吸窘迫综合征(RDS)等复杂疾病的发病机制。表面活性物质蛋白(SPs)在肺功能中起重要作用,这些蛋白的基因变异与包括RDS在内的肺部疾病有关。为了确定SP - A和SP - D的单倍型从父母向患有RDS的后代传递是否不成比例,我们推测这些SP基因以前未被研究的遗传单倍型与RDS的发病有关。

方法

收集了132个患有RDS的新生儿家庭的DNA。进行基因分型,并通过传递不平衡检验确定从父母到后代的单倍型传递情况。

结果

双标记SP - D/SP - A单倍型DA160_A/SP - A2 1A(1)对RDS的发生具有保护作用(p = 0.035)。包含来自显著双标记单倍型的一个或两个位点的四种三标记和四标记单倍型也对RDS的发生具有保护作用。

结论

这些数据确定了针对RDS的保护性单倍型,并支持了与患RDS儿童的SP基因差异相关的研究结果。对具有遗传和环境风险因素的复杂疾病中的单倍型进行研究,可能有助于更好地理解这类疾病。

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