Tampere University Hospital, Tampere, Finland.
Centre for Child Health Research, Tampere University and University Hospital, Tampere, Finland.
Sci Rep. 2017 Jun 7;7(1):2956. doi: 10.1038/s41598-017-03429-x.
Toll-like receptors (TLRs) recognise microbes that contribute to the severity of bronchiolitis and the subsequent risk of asthma. We evaluated whether post-bronchiolitis asthma was associated with polymorphisms in the TLR3 rs3775291, TLR4 rs4986790, TLR7 rs179008, TLR8 rs2407992, TLR9 rs187084, and TLR10 rs4129009 genes. The gene polymorphisms were studied at the age of 6.4 years (mean) in 135 children hospitalised for bronchiolitis in infancy. The outcome measure was current or previous asthma. Current asthma was more common (30%) in children with the variant AG or GG genotype in the TLR10 rs4129009 gene versus those who were homozygous for the major allele A (11%) (p = 0.03). The adjusted odds ratio (aOR) was 4.30 (95% CI 1.30-14.29). Asthma ever was more common (34.6%) in girls with the TLR7 variant AT or TT genotype versus those who were homozygous for the major allele A (12.5%) (p = 0.03). The adjusted OR was 3.93 (95% CI 1.06-14.58). Corresponding associations were not seen in boys. There were no significant associations between TLR3, TLR4, TLR8, or TLR9 polymorphisms and post-bronchiolitis asthma. Polymorphism in the TLR10 gene increases and in the TLR7 gene may increase the risk of asthma in preschool-aged children after infant bronchiolitis.
Toll 样受体 (TLRs) 识别导致细支气管炎严重程度和随后哮喘风险的微生物。我们评估了细支气管炎后哮喘是否与 TLR3 rs3775291、TLR4 rs4986790、TLR7 rs179008、TLR8 rs2407992、TLR9 rs187084 和 TLR10 rs4129009 基因的多态性有关。在婴儿时期因细支气管炎住院的 135 名儿童 6.4 岁(平均年龄)时研究了基因多态性。结果测量是当前或以前的哮喘。TLR10 rs4129009 基因中变异型 AG 或 GG 基因型的儿童中当前哮喘更为常见(30%),而主要等位基因 A 纯合子的儿童为 11%(p=0.03)。调整后的优势比(aOR)为 4.30(95%CI 1.30-14.29)。TLR7 变异型 AT 或 TT 基因型的女孩中,哮喘曾经更为常见(34.6%),而主要等位基因 A 纯合子的女孩为 12.5%(p=0.03)。调整后的 OR 为 3.93(95%CI 1.06-14.58)。在男孩中没有观察到相应的关联。TLR3、TLR4、TLR8 或 TLR9 多态性与细支气管炎后哮喘之间没有显著关联。TLR10 基因的多态性增加,TLR7 基因的多态性可能增加婴幼儿细支气管炎后学龄前儿童患哮喘的风险。