Department of Pediatrics, Zhejiang Chinese Medicine and Western Medicine Integrated Hospital/Hangzhou Red Cross Hospital, Hangzhou, Zhejiang, China.
Department of Pediatrics, Hangzhou Children's Hospital, Hangzhou, Zhejiang, China.
Genet Test Mol Biomarkers. 2020 Dec;24(12):761-770. doi: 10.1089/gtmb.2020.0122. Epub 2020 Dec 2.
To study the relationships between single nucleotide polymorphisms (SNPs) in the intron of the tumor necrosis factor α () gene and the susceptibility and severity of disease associated with adenovirus infection in children. Four polymorphic loci of the gene (rs3093661, rs1800610, rs3093662, and rs3093664) were characterized allelically and genotypically in 320 children with adenovirus-associated pneumonia (AP) and compared with 320 healthy controls. Enzyme-linked immunosorbent assays (ELISAs) were used to detect the plasma TNFα protein levels in all subjects. The gene rs3093661 locus A allele, the rs1800610 locus A allele, the rs3093662 locus G allele, and the rs3093664 locus G allele were identified as susceptibility alleles for development of AP, and they were also positively correlated with the severity of AP. In children who had the GGAA haplotype, AP susceptibility was significantly reduced (0.28-fold) (95% confidence interval, CI: 0.20-0.40, < 0.001). Conversely, among the subjects with the AGGG haplotype, their AP susceptibility risk was significantly increased (2.76-fold) (95% CI: 1.77-4.29, < 0.001); and in the subjects with the AP GGGG haplotype their AP susceptibility risk was significantly increased (2.49-fold) (95% CI: 1.67-3.72, < 0.001). The rs3093661, rs1800610, rs3093662, and rs3093664 SNPs were significantly correlated with plasma TNFα levels ( < 0.05). The gene rs3093661, rs1800610, rs3093662, and rs3093664 loci are associated with AP susceptibility and severity. This relationship might be due to the effect on TNFα levels found in the plasma. Clinical Trial Registration number: LL20190723.
研究肿瘤坏死因子 α(TNF-α)基因内含子中单核苷酸多态性(SNPs)与儿童腺病毒感染相关疾病的易感性和严重程度的关系。对 320 例腺病毒相关性肺炎(AP)患儿和 320 例健康对照者的 TNF-α 基因 4 个多态性位点(rs3093661、rs1800610、rs3093662 和 rs3093664)进行了等位基因和基因型特征分析。所有受试者均采用酶联免疫吸附试验(ELISA)检测血浆 TNFα 蛋白水平。TNF-α 基因 rs3093661 位点 A 等位基因、rs1800610 位点 A 等位基因、rs3093662 位点 G 等位基因和 rs3093664 位点 G 等位基因被确定为发生 AP 的易感等位基因,且与 AP 的严重程度呈正相关。在 GGAA 单倍型的患儿中,AP 的易感性显著降低(0.28 倍)(95%置信区间,CI:0.20-0.40,<0.001)。相反,在具有 AGGG 单倍型的受试者中,其 AP 的易感性风险显著增加(2.76 倍)(95%CI:1.77-4.29,<0.001);而具有 APGGG 单倍型的患儿,其 AP 的易感性风险显著增加(2.49 倍)(95%CI:1.67-3.72,<0.001)。TNF-α 基因 rs3093661、rs1800610、rs3093662 和 rs3093664 单核苷酸多态性与血浆 TNFα 水平显著相关(<0.05)。TNF-α 基因 rs3093661、rs1800610、rs3093662 和 rs3093664 位点与 AP 的易感性和严重程度有关。这种关系可能是由于血浆中 TNFα 水平的影响。临床试验注册号:LL20190723。