Plaza-Serón María Del Carmen, Blanca-López Natalia, Pérez-Sánchez Natalia, Doña Inmaculada, Acosta-Herrera Marialbert, Pino-Yanes María, Flores Carlos, Cornejo-García José Antonio, Perkins James R, Molina Ana, Torres Maria José, Blanca Miguel, Canto María Gabriela, Ayuso Pedro
Allergy Service, Infanta Leonor Hospital, Instituto de Salud Carlos III, Madrid, Spain.
Int Arch Allergy Immunol. 2016;169(4):249-55. doi: 10.1159/000444797. Epub 2016 May 31.
Nonsteroidal anti-inflammatory drugs (NSAIDs) are the most frequent agents involved in hypersensitivity drug reactions, with NSAID-induced urticaria and/or angioedema (NIUA) being the most common entity. Mast cells are key players in NIUA and are activated by thymic stromal lymphopoietin (TSLP). This cytokine functions through recognition by its receptor, composed of IL7Rα (interleukin-7 receptor alpha) and TSLPR (TSLP receptor). These genes have been previously associated with other inflammatory diseases.
We assessed the genetic association between single nucleotide polymorphisms (SNPs) in TSLP, IL7R and TSLPR and NIUA in Spanish individuals, using genotyped and imputed data. A total of 369 unrelated NIUA patients and 580 NSAID-tolerant control subjects were included, and 6 SNPs in TSLP, 6 in IL7R and 3 in TSLPR were genotyped. Further variants were imputed using Mach and the 1,000 Genomes Project (Phase 3) data. Association testing and statistical analyses were performed with Mach2dat and R.
A total of 139 SNPs were tested for association following quality control. Two SNPs in TSLP (rs1816678 and rs764917) showed a nominal association (p = 0.033 and 0.024, respectively) with NIUA, although these results were not statistically significant after correcting for multiple comparisons.
Although TSLP, IL7R and TSLPR are important genes involved in the development of the inflammatory response, we found no significant genetic association with NIUA in our population for common SNPs in these genes.
非甾体抗炎药(NSAIDs)是引起药物超敏反应最常见的药物,其中NSAID诱导的荨麻疹和/或血管性水肿(NIUA)最为常见。肥大细胞是NIUA的关键参与者,并由胸腺基质淋巴细胞生成素(TSLP)激活。这种细胞因子通过其受体发挥作用,该受体由IL7Rα(白细胞介素-7受体α)和TSLPR(TSLP受体)组成。这些基因先前已与其他炎症性疾病相关联。
我们使用基因分型和推算数据评估了西班牙人群中TSLP、IL7R和TSLPR单核苷酸多态性(SNP)与NIUA之间的遗传关联。共纳入369例无亲缘关系的NIUA患者和580例对NSAID耐受的对照受试者,对TSLP中的6个SNP、IL7R中的6个SNP和TSLPR中的3个SNP进行基因分型。使用Mach和千人基因组计划(第3阶段)数据推算其他变异。使用Mach2dat和R进行关联测试和统计分析。
在质量控制后,共对139个SNP进行了关联测试。TSLP中的两个SNP(rs1816678和rs764917)与NIUA显示出名义上的关联(p分别为0.033和0.024),尽管在进行多重比较校正后这些结果无统计学意义。
尽管TSLP、IL7R和TSLPR是参与炎症反应发展的重要基因,但我们在人群中未发现这些基因的常见SNP与NIUA有显著的遗传关联。