Association of asthma with a functional promoter polymorphism in the IL16 gene

被引:35
作者
Burkart, KM
Barton, SJ
Holloway, JW
Yang, IA
Cakebread, JA
Cruikshank, W
Little, F
Jin, XY
Farrier, LA
Clough, JB
Keith, TP
Holgate, S
Center, DM
O'Connor, GT
机构
[1] Boston Univ, Sch Med, Ctr Pulm, Dept Med, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Genet Program, Dept Med, Boston, MA 02118 USA
[3] Boston Univ, Sch Med, Dept Neurol, Boston, MA 02118 USA
[4] Boston Univ, Sch Med, Dept Genet & Genom, Boston, MA 02118 USA
[5] Boston Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[6] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA USA
[7] Univ Southampton, Human Genet Res Div, Sch Med, Southampton, Hants, England
[8] Univ Southampton, Resp Cell & Mol Biol Infect Inflammat & Repair Di, Sch Med, Southampton, Hants, England
[9] Oscient Pharmaceut, Dept Human Genet, Waltham, MA USA
基金
英国医学研究理事会;
关键词
asthma; IL-16; genetic epidemiology; family-based association test; atopy; single nucleotide polymorphism;
D O I
10.1016/j.jaci.2005.10.011
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: IL-16, a multifunctional cytokine with increased expression in the airways of asthmatic subjects, inhibits allergic airway inflammation in animal models. A T -> C single nucleotide polymorphism (SNP) at the -295 position in the promoter region of the IL16 gene has been described. Objective: We sought to examine the functional significance of this promoter SNP and its relationship to asthma. Methods: We examined the effect of the -295 SNP on promoter activity in cell-line (HBE4-E6/E7) transfection experiments. We investigated the association of the IL16 -295 genotype with asthma among 341 affected sib-pair white families and 184 unrelated nonasthmatic control subjects. We analyzed the association between the IL16 genotype and asthma using family-based association test and case-control analyses. Results: In in vitro transfection experiments the T allele in the -295 position was associated with substantially reduced promoter activity compared with the C allele. In the family study the more common T allele at the -295 position was significantly associated with all asthma phenotypes (P = .002 to P = .015). In the case-control analysis asthmatic subjects were more likely than unrelated nonasthmatic control subjects to have the -295 TT genotype, but this did not reach statistical significance (odds ratio, 1.36; 95% CI, 0.92-2.02). Conclusions: The T allele at the -295 position in the IL16 promoter region is associated with reduced promoter activity relative to the C allele and with asthma in this white population. Further investigation is needed to delineate the mechanisms underlying these findings and the relationship of the IL16 -295 genotype to asthma in other populations.
引用
收藏
页码:86 / 91
页数:6
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