Jurado-Escobar Raquel, Doña Inmaculada, Triano-Cornejo José, Perkins James R, Pérez-Sánchez Natalia, Testera-Montes Almudena, Labella Marina, Bartra Joan, Laguna José J, Estravís Miguel, Agúndez José A G, Torres María J, Cornejo-García José A
Allergy Research Group, Instituto De Investigación Biomédica De Málaga-IBIMA, Malaga, Spain.
Departamento De Medicina, Universidad De Málaga, Malaga, Spain.
Front Pharmacol. 2021 Apr 30;12:667824. doi: 10.3389/fphar.2021.667824. eCollection 2021.
Nonsteroidal anti-inflammatory drugs (NSAIDs) are among the main triggers of drug hypersensitivity reactions, probably due to their high consumption worldwide. The most frequent type of NSAID hypersensitivity is NSAID cross-hypersensitivity, in which patients react to NSAIDs from different chemical groups in the absence of a specific immunological response. The underlying mechanism of NSAID cross-hypersensitivity has been linked to cyclooxygenase (COX)-1 inhibition causing an imbalance in the arachidonic acid pathway. Despite NSAID-induced acute urticaria/angioedema (NIUA) being the most frequent clinical phenotype, most studies have focused on NSAID-exacerbated respiratory disease. As NSAID cross-hypersensitivity reactions are idiosyncratic, only appearing in some subjects, it is believed that individual susceptibility is under the influence of genetic factors. Although associations with polymorphisms in genes from the AA pathway have been described, no previous study has evaluated the potential role of cytosolic phospholipase A2 (cPLA2) variants. This enzyme catalyzes the initial hydrolysis of membrane phospholipids to release AA, which can be subsequently metabolized into eicosanoids. Here, we analyzed for the first time the overall genetic variation in the cPLA2 gene (PLA2G4A) in NIUA patients. For this purpose, a set of tagging single nucleotide polymorphisms (tagSNPs) in PLA2G4A were selected using data from Europeans subjects in the 1,000 Genomes Project, and genotyped with the iPlex Sequenom MassArray technology. Two independent populations, each comprising NIUA patients and NSAID-tolerant controls, were recruited in Spain, for the purposes of discovery and replication, comprising a total of 1,128 individuals. Fifty-eight tagSNPs were successfully genotyped in the discovery cohort, of which four were significantly associated with NIUA after Bonferroni correction (rs2049963, rs2064471, rs12088010, and rs12746200). These polymorphisms were then genotyped in the replication cohort: rs2049963 was associated with increased risk for NIUA after Bonferroni correction under the dominant and additive models, whereas rs12088010 and rs12746200 were protective under these two inheritance models. Our results suggest a role for PLA2G4A polymorphisms in NIUA. However, further studies are required to replicate our findings, elucidate the mechanistic role, and evaluate the participation of PLA2G4A variants in other phenotypes induced by NSAID cross-hypersensitivity.
非甾体抗炎药(NSAIDs)是药物超敏反应的主要诱因之一,这可能是由于其在全球范围内的高消费量。最常见的NSAID超敏反应类型是NSAID交叉超敏反应,即患者在没有特异性免疫反应的情况下对不同化学组的NSAIDs产生反应。NSAID交叉超敏反应的潜在机制与环氧化酶(COX)-1抑制导致花生四烯酸途径失衡有关。尽管NSAID诱导的急性荨麻疹/血管性水肿(NIUA)是最常见的临床表型,但大多数研究都集中在NSAID加重的呼吸道疾病上。由于NSAID交叉超敏反应是特异质性的,仅在某些个体中出现,因此认为个体易感性受遗传因素影响。尽管已经描述了与花生四烯酸途径基因多态性的关联,但之前没有研究评估过胞质磷脂酶A2(cPLA2)变体的潜在作用。这种酶催化膜磷脂的初始水解以释放花生四烯酸,随后花生四烯酸可被代谢为类二十烷酸。在此,我们首次分析了NIUA患者中cPLA2基因(PLA2G4A)的总体遗传变异。为此,利用千人基因组计划中欧洲受试者的数据,在PLA2G4A中选择了一组标签单核苷酸多态性(tagSNPs),并采用iPlex Sequenom MassArray技术进行基因分型。在西班牙招募了两个独立的人群,每个群体都包括NIUA患者和对NSAIDs耐受的对照,用于发现和验证,总共1128人。在发现队列中成功对58个tagSNPs进行了基因分型,其中4个在Bonferroni校正后与NIUA显著相关(rs2049963、rs2064471、rs12088010和rs12746200)。然后在验证队列中对这些多态性进行基因分型:在显性和加性模型下,Bonferroni校正后rs2049963与NIUA风险增加相关,而rs12088010和rs12746200在这两种遗传模型下具有保护作用。我们的结果表明PLA2G4A多态性在NIUA中起作用。然而,需要进一步的研究来重复我们的发现,阐明其机制作用,并评估PLA2G4A变体在NSAID交叉超敏反应诱导的其他表型中的参与情况。