Transmission of Surfactant Protein Variants and Haplotypes in Children Hospitalized With Respiratory Syncytial Virus

被引:42
作者
Thomas, Neal J. [1 ,2 ]
Diangelo, Susan [1 ]
Hess, Joseph C. [1 ]
Fan, Ruzong [4 ]
Ball, Margaret W. [5 ]
Geskey, Joseph M. [1 ]
Willson, Douglas F. [5 ]
Floros, Joanna [1 ,3 ]
机构
[1] Penn State Univ, Coll Med, Dept Pediat, Hershey, PA 17033 USA
[2] Penn State Univ, Coll Med, Dept Publ Hlth Sci, Hershey, PA 17033 USA
[3] Penn State Univ, Coll Med, Dept Obstet & Gynecol, Hershey, PA 17033 USA
[4] Texas A&M Univ, Dept Stat, College Stn, TX 77843 USA
[5] Univ Virginia, Dept Pediat, Charlottesville, VA 22908 USA
基金
美国国家卫生研究院;
关键词
A GENE LOCUS; ACUTE BRONCHIOLITIS; DISTRESS-SYNDROME; TEST TDT; ASSOCIATION; INFECTION; INFANTS; RISK; DISEQUILIBRIUM; PHAGOCYTOSIS;
D O I
10.1203/PDR.0b013e3181a1d768
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Severity of lung injury with respiratory syncytial virus (RSV) infection is variable and may be related to genetic variations. This preliminary report describes a prospective, family-based association study of children hospitalized secondary to RSV, aimed to determine whether intragenic and other haplotypes of surfactant proteins (SP)-A and SP-D are transmitted disproportionately from parents to offspring with RSV disease. Genomic DNA was genotyped for several SP-A and SP-D single nucleotide polymorphisms (SNPs). Transmission disequilibrium test analysis was used to determine transmission of variants and haplotypes from parents to affected offspring. Three hundred seventy-five individuals were studied, including 148 children with active RSV disease and one or both parents. The SP-A2 intragenic haplotype 1A(2) was found to be protective (p = 0.013). The SP-D SNP DA160_A may possibly be an "at-risk" marker (p = 0.0058). Additional two- and three-marker haplotypes were associated with severe RSV disease with two being protective (DA11+T/DA160_G and DA160_G/SP-A2 1A(0)/SP-A1 6A(2)). We conclude that there may be associations between SP-A and SP-D and RSV disease. Further study is required to determine whether these variants can be used to target a high-risk patient population in clinical trials aimed at reducing either the symptoms of acute infection or long-term pulmonary sequelae. (Pediatr Res 66: 70-73, 2009)
引用
收藏
页码:70 / 73
页数:4
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