Esposito Susanna, Ierardi Valentina, Daleno Cristina, Scala Alessia, Terranova Leonardo, Tagliabue Claudia, Rios Walter Peves, Pelucchi Claudio, Principi Nicola
Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Via Commenda 9, 20122 Milan, Italy.
BMC Pulm Med. 2014 Oct 18;14:162. doi: 10.1186/1471-2466-14-162.
Wheezing during early life is a very common disorder, but the reasons underlying the different wheezing phenotypes are still unclear. The aims of this study were to analyse the potential correlations between the risk of developing recurrent wheezing and the presence of specific polymorphisms of some genes regulating immune system function, and to study the relative importance of the associations of different viruses and genetic polymorphisms in causing recurrent episodes.
The study involved 119 otherwise healthy infants admitted to hospital for a first episode of wheezing (74 of whom subsequently experienced recurrent episodes) and 119 age- and sex-matched subjects without any history of respiratory problem randomly selected from those attending our outpatient clinic during the study period. All of the study subjects were followed up for two years, and 47 single nucleotide polymorphisms (SNPs) in 33 candidate genes were genotyped on whole blood using an ABI PRISM 7900 HT Fast Real-time instrument.
IL8-rs4073AT, VEGFA-rs833058CT, MBL2-rs1800450CT and IKBKB-rs3747811AT were associated with a significantly increased risk of developing wheezing (p = 0.02, p = 0.03, p = 0.05 and p = 0.0018), whereas CTLA4-rs3087243AG and NFKBIB-rs3136641TT were associated with a significantly reduced risk (p = 0.05 and p = 0.04). IL8-rs4073AT, VEGFA-rs2146323AA and NFKBIA-rs2233419AG were associated with a significantly increased risk of developing recurrent wheezing (p = 0.04, p = 0.04 and p = 0.03), whereas TLR3-rs3775291TC was associated with a significantly reduced risk (p = 0.03). Interestingly, the study of gene-environment interactions showed that rhinovirus was significantly associated with recurrent wheezing in the presence of IL4Ra-rs1801275GG and G (odds ratio [OR] 6.03, 95% confidence interval [CI]: 1.21-30.10, p = 0.03) and MAP3K1-rs702689AA (OR 4.09, 95% CI: 1.14-14.61, p = 0.03).
This study shows a clear relationship between the risk of wheezing and polymorphisms of some genes involved in the immune response. Although further studies are needed to confirm the results, these findings may be useful for the early identification of children at the highest risk of developing recurrent episodes and possibly subsequent asthma.
生命早期喘息是一种非常常见的病症,但不同喘息表型背后的原因仍不清楚。本研究的目的是分析复发性喘息风险与一些调节免疫系统功能的基因特定多态性之间的潜在相关性,并研究不同病毒与基因多态性在引起复发发作中的相对重要性。
本研究纳入了119名因首次喘息发作而入院的健康婴儿(其中74名随后经历了复发发作),以及119名在研究期间从我院门诊随机选取的年龄和性别匹配、无任何呼吸问题病史的受试者。所有研究对象均随访两年,使用ABI PRISM 7900 HT Fast Real-time仪器对全血中的33个候选基因中的47个单核苷酸多态性(SNP)进行基因分型。
IL8-rs4073AT、VEGFA-rs833058CT、MBL2-rs1800450CT和IKBKB-rs3747811AT与喘息发生风险显著增加相关(p = 0.02、p = 0.03、p = 0.05和p = 0.0018),而CTLA4-rs3087243AG和NFKBIB-rs3136641TT与风险显著降低相关(p = 0.05和p = 0.04)。IL8-rs4073AT、VEGFA-rs2146323AA和NFKBIA-rs2233419AG与复发性喘息发生风险显著增加相关(p = 0.04、p = 0.04和p = 0.03),而TLR3-rs3775291TC与风险显著降低相关(p = 0.03)。有趣的是,基因-环境相互作用研究表明,在存在IL4Ra-rs1801275GG和G时,鼻病毒与复发性喘息显著相关(比值比[OR] 6.03,95%置信区间[CI]:1.21 - 30.10,p = 0.03),以及与MAP3K1-rs702689AA相关(OR 4.09,95% CI:1.14 - 14.61,p = 0.03)。
本研究表明喘息风险与一些参与免疫反应的基因多态性之间存在明确关系。尽管需要进一步研究来证实结果,但这些发现可能有助于早期识别发生复发发作及可能随后发生哮喘风险最高的儿童。