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首页> 外文期刊>Journal of Thoracic Disease >Relation between inflammatory cytokine levels in serum and bronchoalveolar lavage fluid and gene polymorphism in young adult patients with bronchiectasis
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Relation between inflammatory cytokine levels in serum and bronchoalveolar lavage fluid and gene polymorphism in young adult patients with bronchiectasis

机译:青年成人支气管扩张患者血清和支气管肺泡灌洗液中炎症细胞因子水平与基因多态性的关系

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摘要

Aim: Bronchiectasis develops as a result of genetic and environmental factors and its etiopathogenesis is not still clear. Recent studies have revealed that inflammatory cytokines, which are formed as a result of chronic infection and inflammation, play a role in the pathogenesis of bronchiectasis. For this purpose, the level of inflammatory cytokines in bronchiectasis and the presence or absence of a genetic predisposition with the gene polymorphism of these cytokines was investigated. Material and methods: A total of 60 patients, 40 study cases and 20 controls, which were monitored with the diagnosis of bronchiectasis were included in the study. In these individuals, cytokine levels [interleukin (IL)-6, IL-8, IL-10, and tumor necrosis factor (TNF)-α] in serum and bronchoalveolar lavage (BAL) fluid, along with the routine blood tests, were determined. Furthermore, the polymorphism in IL-6, IL-8, IL-10, and TNF-α cytokine genes and its frequency were studied in the obtained DNA by the automatic sequence analysis method and the results were compared. Findings: It was found that in serum and BAL fluid of the patient group, the IL-8 level was high, whereas the IL-10 level was low (P0.05). No significant difference was detected in the other cytokines (P>0.05). It was found that in cytokine gene polymorphisms IL-8 -251 A/T, IL-10 -592 A/C, and IL-10 -819 T/C genotypes are associated with increased risk of bronchiectasis. It was detected that the IL-8 -251 A/T genotype increased the risk of having the disease by 4.19 fold. (OR =4.19, 95% CI =1.24-14.17, P=0.021). The IL-10 -592 C/A genotype increased the risk of having the disease by 5.71 fold (OR = 5.71, 95% CI = 1.35-24.06, P=0.017) and the IL-10 -819 T/C genotype increased the risk of having the disease by 5.06 fold (OR =5.06, 95% CI =1.20-21.27, P=0.048). No significant correlation was found between the other polymorphisms and bronchiectasis. Conclusions: The IL-8, IL-10 levels and the gene polymorphism of these cytokines differ. In addition to detecting higher levels of pro-inflammatory IL-8 and lower levels of anti-inflammatory IL-10, detection of gene polymorphism related to these two cytokines in bronchiectasis gives rise to the thought that cytokines may have role in a predisposition to bronchiectasis. However, as the number of patients is small, precise remarks could not be made on this subject. There is need for further studies include a larger number of patients.
机译:目的:支气管扩张是由于遗传和环境因素导致的,其病因尚未明确。最近的研究表明,由慢性感染和炎症形成的炎性细胞因子在支气管扩张的发病机理中起作用。为了这个目的,研究了支气管扩张中炎性细胞因子的水平以及这些细胞因子的基因多态性是否存在遗传易感性。材料与方法:本研究共纳入了60例患者,40例研究病例和20例对照,这些患者均以支气管扩张的诊断进行了监测。在这些个体中,血清和支气管肺泡灌洗液(BAL)液中的细胞因子水平[白介素(IL)-6,IL-8,IL-10和肿瘤坏死因子(TNF)-α]以及常规的血液检查结果为决心。此外,通过自动序列分析方法研究了获得的DNA中IL-6,IL-8,IL-10和TNF-α细胞因子基因的多态性及其频率。结果:发现患者组的血清和BAL液中IL-8水平较高,而IL-10水平较低(P <0.05)。其他细胞因子差异均无统计学意义(P> 0.05)。发现在细胞因子基因多态性中,IL-8 -251 A / T,IL-10 -592 A / C和IL-10 -819 T / C基因型与支气管扩张风险增加有关。检测到IL-8 -251 A / T基因型使患该疾病的风险增加了4.19倍。 (OR = 4.19,95%CI = 1.24-14.17,P = 0.021)。 IL-10 -592 C / A基因型使患病的风险增加了5.71倍(OR = 5.71,95%CI = 1.35-24.06,P = 0.017),IL-10 -819 T / C基因型使患病的风险增加了。患病风险增加5.06倍(OR = 5.06,95%CI = 1.20-21.27,P = 0.048)。其他多态性与支气管扩张之间未发现显着相关性。结论:这些细胞因子的IL-8,IL-10水平和基因多态性存在差异。除了检测较高水平的促炎性IL-8和较低水平的抗炎性IL-10外,检测与支气管扩张中这两种细胞因子相关的基因多态性还引发了这样的想法:细胞因子可能在支气管扩张的易感性中起作用。但是,由于患者人数很少,因此无法对此主题进行精确描述。需要进一步的研究,包括更多的患者。

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