BIOMARKERS OF INFLAMMATION AT BRONCHIAL ASTHMA IN CHILDREN WITH ALTERNATIVE DEBUT OF THE DISEASE

O. Koloskova, Т. Bilous, О.P. Korotun, F. Herman, V. Bilous, S. I. Seliverstov
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引用次数: 1

Abstract

Objectives - to analyze the activity of the inflammatory process in the airways of childrenwith bronchial asthma depending on different onset of the disease.Material and methods. Keeping to the principles of bioethics a comprehensiveretrospective examination of 319 children suffering from BA was performed. In 257children (clinical group I) bronchial asthma developed against a background of chronicobstructive bronchitis. The second clinical group included 43 children, in whom asthmadebuted after community-acquired pneumonia. The third (III) clinical group consistedof 19 children in whom asthma was first verified after inpatient treatment for asthmaticstatus.Results. According to the severity of bronchial asthma, it was found that the representativesof the III clinical group, compared with other patients, significantly more often had a severecourse of the disease. For patients of the I clinical group in the debut it is characterizedby increased eosinophils and decreased neutrophil counts in sputum, for patients ofgroup II - increased eosinophils and epitheliocytes, but a decrease in lymphocytes, andfor children of clinical group III - low eosinophils sputum with a simultaneous increasein neutrophils. In particular, a statistically significant increase in the content of VEGF,a decrease in the content of cationic proteins, MMP-9, and interleukins-6, and -13 inthe sputum indicates the predominance of neoangiogenesis in children of clinical groupIII. Instead, in the representatives of the II clinical group the remodeling processes weremainly caused by the inflammatory process with the release of intracellular eosinophiliccationic proteins.Conclusion. These data indicate the discrete nature of the type and severity of theinflammatory process of the respiratory tract in the dynamics of observation in childrenof clinical comparison groups, which suggests the presence of certain phenotypicdifferences due to the alternative onset of the disease, which in its turn was determinedby different triggers. Such deviations of the inflammatory process indicate that patientswith asthma require a personalized approach to differentiated diagnostic monitoring andtargeted anti-inflammatory treatment, taking into account the peculiarities of the onsetof the disease.
儿童支气管哮喘的炎症生物标志物与疾病的替代首发
目的-分析支气管哮喘患儿气道炎症过程的活动性,这取决于疾病的不同发作。材料和方法。遵循生命伦理学的原则,对319名患有BA的儿童进行了全面的回顾性检查。257例儿童(临床ⅰ组)支气管哮喘发病背景为慢性阻塞性支气管炎。第二个临床组包括43名儿童,他们在社区获得性肺炎后首次出现哮喘。第三(III)临床组包括19名儿童,其中哮喘是在住院治疗后首次证实的。根据支气管哮喘的严重程度,我们发现具有代表性的临床III组,与其他患者相比,明显更常出现严重的病程。临床第一组患者的特点是痰中嗜酸性粒细胞增多,中性粒细胞减少;临床第二组患者的特点是痰中嗜酸性粒细胞和上皮细胞增多,但淋巴细胞减少;临床第三组患儿的特点是痰中嗜酸性粒细胞减少,同时嗜中性粒细胞增多。特别是痰中VEGF含量显著升高,阳离子蛋白、MMP-9、白细胞介素-6、-13含量降低,具有统计学意义,说明临床piii组患儿新生血管生成占优势。相反,在II临床组的代表中,重塑过程主要是由细胞内嗜酸性蛋白释放的炎症过程引起的。这些数据表明,在临床对照组儿童的动态观察中,呼吸道炎症过程的类型和严重程度具有离散性,这表明由于疾病的不同发病而存在一定的表型差异,而疾病的发病又由不同的触发因素决定。这种炎症过程的偏差表明,考虑到疾病发病的特殊性,哮喘患者需要个性化的方法来区分诊断监测和靶向抗炎治疗。
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