Asan Institute for Life Science, Asan Medical Center, Seoul, South Korea.
Hum Immunol. 2012 Sep;73(9):954-9. doi: 10.1016/j.humimm.2012.06.009. Epub 2012 Jun 23.
In 2007, a genome-wide association study identified associations between variants involved in the regulation of ORMDL3 expression and asthma. These observations were subsequently replicated in case-control studies in several ethnic groups. We investigated the possible contribution of GSDMB/ORMDL3 variants to asthma susceptibility and intermediate asthma phenotypes in Korean children. The polymorphisms rs7216389, rs4794820, rs4065275, and rs11650680 were genotyped using the TaqMan assay in 931 asthmatics and 480 normal controls in a case-control study, and in 1907 elementary school children in a general population study. Each subject also underwent peripheral blood analysis of immunoglobulin E levels, eosinophil cationic protein (ECP) levels, and eosinophil percentage. Pulmonary function testing (FEV(1) and MMEF) and a methacholine provocation test (PC(20)) were also performed. The case-control study revealed a significant association between a linkage disequilibrium block, including rs7216389, rs4794820, and rs4065275, and susceptibility to asthma and atopic asthma. The CT and TT genotypes of rs11650680 were associated with lower logECP levels than the CC genotype in asthmatics, while the GA and AA genotypes of rs4794820 were associated with higher logPC(20) values than the GG genotype in atopic asthmatics. The haplotype (CAA) of rs7216389, rs4794820 and rs4065275 was associated with a lower risk of asthma susceptibility and a higher logPC(20). In the general population study, rs11650680 was significantly associated with a diagnosis of asthma. Moreover, the GA and AA genotypes of rs4794820 were associated with higher logPC(20) values and lower eosinophil percentages than the GG genotype in subjects who had been diagnosed with asthma, or showed bronchial hyperresponsiveness (PC(20)≤16). The GSDMB/ORMDL3 gene block, which includes rs7216389, rs4065275, rs4794820, and rs11650680, may be associated with asthma susceptibility in Korean children because it promotes eosinophilic inflammation, which induces bronchial hyperresponsiveness.
2007 年,一项全基因组关联研究确定了参与调控 ORMDL3 表达的变异体与哮喘之间的关联。这些观察结果随后在几个种族的病例对照研究中得到了复制。我们研究了 GSDMB/ORMDL3 变异体对韩国儿童哮喘易感性和中间哮喘表型的可能贡献。在病例对照研究中,931 名哮喘患者和 480 名正常对照者使用 TaqMan 测定法对 rs7216389、rs4794820、rs4065275 和 rs11650680 多态性进行了基因分型,在一般人群研究中,对 1907 名小学生进行了基因分型。每个受试者还接受了外周血免疫球蛋白 E 水平、嗜酸性粒细胞阳离子蛋白(ECP)水平和嗜酸性粒细胞百分比的分析。还进行了肺功能测试(FEV1 和 MMEF)和乙酰甲胆碱激发试验(PC20)。病例对照研究显示,包括 rs7216389、rs4794820 和 rs4065275 在内的连锁不平衡块与哮喘易感性和特应性哮喘之间存在显著关联。rs11650680 的 CT 和 TT 基因型与哮喘患者中 ECP 水平的 log 降低有关,而 rs4794820 的 GA 和 AA 基因型与特应性哮喘患者中 PC20 值的 log 升高有关。rs7216389、rs4794820 和 rs4065275 的单倍型(CAA)与哮喘易感性降低和 PC20 的 log 升高有关。在一般人群研究中,rs11650680 与哮喘的诊断显著相关。此外,在被诊断为哮喘或表现出支气管高反应性(PC20≤16)的受试者中,rs4794820 的 GA 和 AA 基因型与较低的嗜酸性粒细胞百分比和较高的 PC20 值有关。包含 rs7216389、rs4065275、rs4794820 和 rs11650680 的 GSDMB/ORMDL3 基因块可能与韩国儿童的哮喘易感性有关,因为它促进嗜酸性粒细胞炎症,从而诱导支气管高反应性。