The von Willebrand factor as a marker of partially controlled asthma severity in children

Q4 Medicine
N.I. Makieieva, V.V. Andrushchenko
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引用次数: 0

Abstract

Asthma is one of the most common chronic non-communicable diseases among adults and children. Recent studies have paid special attention to endothelial dysfunction in the mechanism of development and progression of asthma, on the one hand, and the occurrence of long-term consequences of endothelial damage, on the other hand. Endothelial dysfunction in the modern sense is not only a pathology of the vascular wall but also a deep, complexly organized system of disorders and compensatory and adaptive reactions that originates at the molecular genetic level. Purpose - to improve the knowledge of assessing the levels of von Willebrand factor (VWF) as a marker of endothelial dysfunction in the blood of children with partially controlled asthma. Materials and methods. 94 children participated in the study. Patients were divided into 4 groups: the Group 1 - children with mild persistent asthma (n=59), the Group 2 - moderately severe persistent asthma (n=10), the Group 3 - severe persistent asthma (n=12), and the Group 4 - control group (n=13). The study of VWF was carried out by a standard enzyme-linked immunosorbent assay (ELISA) using the Human VWF ELISA Kit. Data were analyzed using Statsoft Statistica version 8 (Tulsa, OK) and MedCalc statistical software version 17.2. Results. It was found that children with asthma had significantly increased levels of VWF in the blood serum compared to the control group. The highest levels of serum VWF were found in patients with severe asthma. Conclusions. Elevated levels of VWF indicate the presence of endothelial dysfunction. Increased levels of VWF depending on the severity of asthma indicate more severe endothelial damage in children with severe asthma. The research was carried out in accordance with the principles of the Declaration of Helsinki. The research protocol was approved by the Local Ethics Committee of the institution mentioned in the work. Informed consent of parents or their guardians was obtained for conducting research. No conflict of interests was declared by the authors.
血管性血友病因子作为儿童部分控制哮喘严重程度的标志
哮喘是成人和儿童中最常见的慢性非传染性疾病之一。近年来的研究特别关注内皮功能障碍在哮喘发生进展中的机制,以及内皮损伤的长期后果的发生。现代意义上的内皮功能障碍不仅是血管壁的一种病理,而且是一种深层的、复杂的组织紊乱系统,以及起源于分子遗传水平的代偿和适应性反应。目的:提高对部分控制哮喘儿童血液中血管性血友病因子(VWF)作为内皮功能障碍标志物水平评估的认识。材料和方法。94名儿童参与了这项研究。患者分为4组:1组-轻度持续性哮喘患儿(n=59), 2组-中重度持续性哮喘患儿(n=10), 3组-重度持续性哮喘患儿(n=12), 4组-对照组(n=13)。VWF的研究采用标准酶联免疫吸附试验(ELISA),使用Human VWF ELISA Kit。数据分析使用Statsoft Statistica version 8 (Tulsa, OK)和MedCalc统计软件version 17.2。结果。结果发现,与对照组相比,哮喘患儿血清中VWF水平显著升高。血清VWF水平最高的是严重哮喘患者。结论。VWF水平升高表明存在内皮功能障碍。VWF水平的升高取决于哮喘的严重程度,表明严重哮喘患儿内皮损伤更严重。这项研究是按照《赫尔辛基宣言》的原则进行的。研究方案经工作中提到的机构当地伦理委员会批准。在进行研究时获得了父母或其监护人的知情同意。作者未声明存在利益冲突。
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来源期刊
Suchasna pediatriia Ukrayina
Suchasna pediatriia Ukrayina Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.40
自引率
0.00%
发文量
50
审稿时长
8 weeks
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