Hedgehog-interacting protein is a COPD susceptibility gene: the Rotterdam Study

被引:61
|
作者
van Durme, Y. M. T. A. [1 ,2 ,3 ]
Eijgelsheim, M. [3 ]
Joos, G. F. [1 ,2 ]
Hofman, A. [3 ,6 ]
Uitterlinden, A. G. [3 ,4 ,6 ]
Brusselle, G. G. [1 ,2 ,3 ]
Stricker, B. H. Ch. [3 ,4 ,5 ,6 ,7 ]
机构
[1] Univ Ghent, Dept Resp Med, B-9000 Ghent, Belgium
[2] Ghent Univ Hosp, B-9000 Ghent, Belgium
[3] Erasmus Univ, Med Ctr, Dept Epidemiol, NL-3000 DR Rotterdam, Netherlands
[4] Erasmus Univ, Med Ctr, Dept Internal Med, NL-3000 DR Rotterdam, Netherlands
[5] Erasmus Univ, Med Ctr, Dept Netherlands Genom, NL-3000 DR Rotterdam, Netherlands
[6] Netherlands Consortium Healthy Ageing, Netherlands Genom Initiat Sponsored, Rotterdam, Netherlands
[7] Inspectorate Healthcare, The Hague, Netherlands
关键词
Chronic obstructive pulmonary disease; epidemiology of chronic obstructive pulmonary disease; genetics; Hedgehog-interacting protein; OBSTRUCTIVE PULMONARY-DISEASE; SONIC HEDGEHOG; RISK; EPIDEMIOLOGY; PREVALENCE; PATHWAY; BURDEN; GENDER; LOCI;
D O I
10.1183/09031936.00129509
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
The Hedgehog signalling pathway plays an important role in lung morphogenesis and cellular responses to lung injury. A genome- wide association study has demonstrated that two single nucleotide polymorphisms (SNPs) near the Hedgehog- interacting protein (Hip) gene, SNP identifiers rs1828591 and rs13118928, are associated with risk of chronic obstructive pulmonary disease (COPD). The aim of the present study was to validate the observed association between genetic variation near the Hip gene and COPD, and to investigate whether risk estimates were modified by smoking behaviour. The association between the Hip gene SNPs and COPD was investigated in the Rotterdam Study by logistic regression analyses, adjusted for several covariates. In addition, an association meta- analysis was performed that included data from the genome-wide association study on COPD. Both SNPs were significantly associated with risk of COPD (OR 0.80; 95% CI 0.72-0.91). Homozygosity for the minor G allele resulted in a decreased risk of COPD of similar to 40% (95% CI 0.47-.78). There was a significant interaction with the number of pack-years of smoking (p=0.004). The meta- analysis yielded an odds ratio for COPD of 0.80 per additional G allele (p=3.4x10(-9)). Genetic variation near the Hip gene was significantly associated with risk of COPD, depending on the number of pack-years of smoking.
引用
收藏
页码:89 / 95
页数:7
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