首页> 外文期刊>The Journal of Allergy and Clinical Immunology >A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.
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A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.

机译:全基因组全基因分析与过敏性鼻炎和草过敏相关的遗传变异及其与出生顺序的相互作用。

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BACKGROUND: Hay fever or seasonal allergic rhinitis (AR) is a chronic disorder associated with IgE sensitization to grass. The underlying genetic variants have not been studied comprehensively. There is overwhelming evidence that those who have older siblings have less AR, although the mechanism for this remains unclear. OBJECTIVE: We sought to identify common genetic variant associations with prevalent AR and grass sensitization using existing genome-wide association study (GWAS) data and to determine whether genetic variants modify the protective effect of older siblings. METHOD: Approximately 2.2 million genotyped or imputed single nucleotide polymorphisms were investigated in 4 large European adult cohorts for AR (3,933 self-reported cases vs 8,965 control subjects) and grass sensitization (2,315 cases vs 10,032 control subjects). RESULTS: Three loci reached genome-wide significance for either phenotype. The HLA variant rs7775228, which cis-regulates HLA-DRB4, was strongly associated with grass sensitization and weakly with AR (P(grass) = 1.6 x 10(-9); P(AR) = 8.0 x 10(-3)). Variants in a locus near chromosome 11 open reading frame 30 (C11orf30) and leucine-rich repeat containing 32 (LRRC32), which was previously associated with atopic dermatitis and eczema, were also strongly associated with both phenotypes (rs2155219; P(grass) = 9.4 x 10(-9); P(AR) = 3.8 x 10(-8)). The third genome-wide significant variant was rs17513503 (P(grass) = 1.2 x 10(-8); PAR = 7.4 x 10(-7)) which was located near transmembrane protein 232 (TMEM232) and solute carrier family 25, member 46 (SLC25A46). Twelve further loci with suggestive associations were also identified. Using a candidate gene approach, where we considered variants within 164 genes previously thought to be important, we found variants in 3 further genes that may be of interest: thymic stromal lymphopoietin (TSLP), Toll-like receptor 6 (TLR6) and nucleotide-binding oligomerization domain containing 1 (NOD1/CARD4). We found no evidence for variants that modified the effect of birth order on either phenotype. CONCLUSIONS: This relatively large meta-analysis of GWASs identified few loci associated with AR and grass sensitization. No birth order interaction was identified in the current analyses.
机译:背景:花粉症或季节性变应性鼻炎(AR)是与IgE对草过敏相关的慢性疾病。潜在的遗传变异尚未得到全面研究。有大量证据表明,兄弟姐妹年龄较大的人AR较少,尽管其机制尚不清楚。目的:我们试图利用现有的全基因组关联研究(GWAS)数据,确定常见的遗传变异与普遍的AR和草过敏有关,并确定遗传变异是否改变了较老同胞的保护作用。方法:在欧洲的4个大型成人队列中,研究了大约220万个基因分型或估算的单核苷酸多态性(3,933例自我报告的病例与8,965例对照对象)和草敏症(2,315例对10,032例对照对象)。结果:这三个表位达到了全基因组意义。顺式调节HLA-DRB4的HLA变体rs7775228与草敏化密切相关,而与AR弱相关(P(草)= 1.6 x 10(-9); P(AR)= 8.0 x 10(-3)) 。 11号染色体开放阅读框30(C11orf30)和富含亮氨酸的重复序列32(LRRC32)附近的基因座变异以前与特应性皮炎和湿疹有关,也与这两种表型密切相关(rs2155219; P(草)= 9.4 x 10(-9); P(AR)= 3.8 x 10(-8))。第三个基因组范围内的重要变异体是rs17513503(P(草)= 1.2 x 10(-8); PAR = 7.4 x 10(-7)),其位于跨膜蛋白232(TMEM232)和溶质载体家族25的附近46(SLC25A46)。还确定了十二个具有暗示关联的基因座。使用候选基因方法,我们认为先前认为重要的164个基因中的变异,我们在3个其他可能感兴趣的基因中发现了变异:胸腺基质淋巴细胞生成素(TSLP),Toll样受体6(TLR6)和核苷酸包含1的低聚结合域(NOD1 / CARD4)。我们没有发现改变出生顺序对任一表型的影响的变体的证据。结论:GWASs的这项相对较大的荟萃分析确定了与AR和草敏化有关的基因座。在目前的分析中,没有发现出生顺序的相互作用。

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