Toll 样受体 2 (rs5743708) 基因多态性对小儿肺炎的影响:风险和严重程度。

Samar M Abd El-Hamid, Alshaymaa A Abd Elalim, Eatemad N A Mansour, Shimaa Moustafa, Eman M Moazen, W. Abdo, Amal K A Abou Elnour, A. A. Elsheikh
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摘要

小儿肺炎是一种影响儿童的常见呼吸道感染,被认为是全球,尤其是中低收入国家儿童死亡和发病的主要原因。Toll 样受体 2 (TLR2) 是一种重要的受体,参与识别细菌病原体和激活免疫反应。TLR2 的遗传变异可部分解释感染易感性的个体差异。本研究旨在调查 TLR2(rs5743708)变异对小儿肺炎感染风险和严重程度的可能影响。研究对象包括 100 名确诊为肺炎的儿科患者和 100 名年龄和性别匹配的正常对照组。研究人员利用实时聚合酶链反应(PCR)对参与者进行了TLR2(rs5743708)变异基因分型。分析结果显示,与野生同型基因型患者相比,TLR2 (rs5743708) (G/A) 基因型儿童患肺炎的风险高出 2.52 倍(OR:2.52;95% CI:1.32-4.79;p = 0.005)。此外,我们还观察到,TLR2 (rs5743708) (A) 等位基因与儿童感染肺炎的更大风险有关(OR:1.612;95% CI:1.07-2.43;p = 0.023),但对感染严重程度没有显著影响。总之,TLR2(rs5743708)突变型(G/A)基因型和(A)等位基因的儿童患肺炎的风险明显更高,但他们感染严重程度的风险并不高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Toll-like receptor 2 (rs5743708) gene polymorphism in pediatric pneumonia: risk and severity.
Pediatric pneumonia is a common respiratory infection that affects children and is thought to be a major source of mortality and morbidity worldwide, particularly in low- and middle-income nations. Toll-like receptor2 (TLR2) is an important receptor involved in the recognition of bacterial pathogens and the activation of the immune response. Genetic variability in TLR2 may partially explain individual differences in susceptibility to infections. The purpose of this study was to investigate the possible contribution of the TLR2 (rs5743708) variant to the risk and severity of pediatric pneumonia infection. The study included 100 pediatric patients diagnosed with pneumonia and 100 normal controls who were age and gender matched. Real-time polymerase chain reaction (PCR) was used to genotype participants for the TLR2 (rs5743708) variant. The analysis revealed that children with the TLR2 (rs5743708) (G/A) genotype showed a 2.52-fold greater risk of having pneumonia (OR: 2.52; 95% CI: 1.32-4.79; p = 0.005) in comparison with patients who have wild homozygous genotypes. Furthermore, we observed that the TLR2 (rs5743708) (A) allele is connected to a greater risk of pneumonia infection in children (OR: 1.612; 95% CI: 1.07-2.43; p = 0.023) but did not significantly influence infection severity. In conclusion, children with the TLR2 (rs5743708) mutant (G/A) genotype and (A) allele had a significantly higher risk of having pneumonia, but they were not at high risk for the severity of the infection.
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