Zhu Guohua, Whyte Moira K B, Vestbo Jorgen, Carlsen Karin, Carlsen Kai-Håkon, Lenney Warren, Silverman Michael, Helms Peter, Pillai Sreekumar G
Genetics, GlaxoSmithKline, Research Triangle Park, NC 27709, USA.
Eur J Hum Genet. 2008 Sep;16(9):1083-90. doi: 10.1038/ejhg.2008.67. Epub 2008 Apr 2.
The interleukin 18 receptor (IL18R1) gene is a strong candidate gene for asthma. It has been implicated in the pathophysiology of asthma and maps to an asthma susceptibility locus on chromosome 2q12. The possibility of association between polymorphisms in IL18R1 and asthma was examined by genotyping seven SNPs in 294, 342 and 100 families from Denmark, United Kingdom and Norway and conducting family-based association analyses for asthma, atopic asthma and bronchial hyper-reactivity (BHR) phenotypes. Three SNPs in IL18R1 were associated with asthma (0.01131 < or = P < or = 0.01377), five with atopic asthma (0.00066 < or = P < or = 0.00405) and two with BHR (0.01450 < or = P < or = 0.03203) in the Danish population; two SNPs were associated with atopic asthma (0.00397 < or = P < or = 0.01481) and four with BHR (0.00435 < or = P < or = 0.03544) in the UK population; four SNPs showed associations with asthma (0.00015 < or = P < or = 0.03062), two with atopic asthma (0.01269 < or = P < or = 0.04042) and three with BHR (0.00259 < or = P < or = 0.01401) in the Norwegian population; five SNPs showed associations with asthma (0.00005 < or = P < or = 0.03744), five with atopic asthma (0.00001 < or = P < or = 0.04491) and three with BHR (0.03568 < or = P < or = 0.04778) in the combined population. Three intronic SNPs (rs1420099, rs1362348 and rs1974675) showed replicated association for at least one asthma-related phenotype. These results demonstrate significant association between polymorphisms in IL18R1 and asthma.
白细胞介素18受体(IL18R1)基因是哮喘的一个强有力的候选基因。它与哮喘的病理生理学有关,定位于2号染色体q12上的一个哮喘易感位点。通过对来自丹麦、英国和挪威的294个、342个和100个家庭中的7个单核苷酸多态性(SNP)进行基因分型,并对哮喘、特应性哮喘和支气管高反应性(BHR)表型进行基于家系的关联分析,研究了IL18R1基因多态性与哮喘之间的关联可能性。在丹麦人群中,IL18R1基因的3个SNP与哮喘相关(0.01131≤P≤0.01377),5个与特应性哮喘相关(0.00066≤P≤0.00405),2个与BHR相关(0.01450≤P≤0.03203);在英国人群中,2个SNP与特应性哮喘相关(0.00397≤P≤0.01481),4个与BHR相关(0.00435≤P≤0.03544);在挪威人群中,4个SNP与哮喘相关(0.00015≤P≤0.03062),2个与特应性哮喘相关(0.01269≤P≤0.04042),3个与BHR相关(0.00259≤P≤0.01401);在合并人群中,5个SNP与哮喘相关(0.00005≤P≤0.03744),5个与特应性哮喘相关(0.00001≤P≤0.04491),3个与BHR相关(0.03568≤P≤0.04778)。3个内含子SNP(rs1420099、rs1362348和rs1974675)至少与一种哮喘相关表型存在重复关联。这些结果表明IL18R1基因多态性与哮喘之间存在显著关联。