Possibilities of using determination of allelic polymorphism of interleukin-6 G174C and tumour necrosis factor-α G308A genes for the prediction of cardiovascular disorders in children with juvenile idiopathic arthritis

IF 0.1 Q4 PEDIATRICS
A. Artsymovych, O. Oshlianska, O. Okhotnikova, Z. Rossokha, O. Popova, N. Medvedeva, Victoriia Vershigora, I. Chaikovsky, O. Kryvova
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引用次数: 0

Abstract

Objectives: Juvenile idiopathic arthritis is a chronic disease that affects the synovial membrane of the joints, but can also lead to secondary lesions of the cardiovascular system. The most important mechanism of myocardial damage is associated with the effect of proinflammatory cytokines. The aim of the study was to propose a method of early detection of cardiovascular system changes and lesions in patients with juvenile idiopathic arthritis based on the determination of allelic polymorphism combined with electrocardiography data. Materials and methods: 102 patients with juvenile idiopathic arthritis underwent a general clinical examination. The overall activity of juvenile idiopathic arthritis was assessed using the Juvenile Arthritis Disease Activity Score. In addition, the patients underwent an electrocardiographic evaluation using the software and hardware complex “Cardioplus P,” which is a portable electrocardiograph providing “signal-averaged” electrocardiography performing the recognition and measurement of amplitude-time parameters, and calculation of secondary electrocardiography parameters. The genotypes of patients were additionally determined by alleles of the TNF-α (G308A) and IL6 (G174C) genes by polymerase chain reaction. Results: The overall number of mutations affects the course of the disease, with two or more mutations being associated with a more aggressive course of the disease, a more pronounced degree of inflammation, and a higher frequency of extra-articular lesions. The complex indicator of the functional state of the myocardium according to the electrocardiography data differed significantly (p = 0.00001) in clusters. Conclusion: Patients with juvenile idiopathic arthritis with two or more mutations in different genes of proinflammatory cytokines have a higher activity of the inflammatory process and a higher frequency of cardiovascular changes according to 4th generation electrocardiography. The determination of polymorphism may be useful in evaluating the risk of development of cardiovascular system abnormalities.
利用白细胞介素-6 G174C和肿瘤坏死因子-α G308A基因等位基因多态性测定预测幼年特发性关节炎儿童心血管疾病的可能性
目的:青少年特发性关节炎是一种影响关节滑膜的慢性疾病,但也可导致心血管系统的继发性病变。心肌损伤最重要的机制与促炎细胞因子的作用有关。本研究的目的是提出一种基于等位基因多态性测定结合心电图数据早期检测幼年特发性关节炎患者心血管系统改变和病变的方法。材料与方法:对102例青少年特发性关节炎患者进行了常规临床检查。使用幼年关节炎疾病活动度评分评估幼年特发性关节炎的总体活动度。此外,患者进行了心电图评估,使用软件和硬件复杂的“Cardioplus P”,这是一种便携式心电图仪,提供“信号平均”心电图,执行振幅-时间参数的识别和测量,并计算二次心电图参数。采用聚合酶链反应检测肿瘤坏死因子-α (G308A)和白细胞介素6 (G174C)基因的等位基因。结果:突变的总数影响疾病的进程,两个或更多的突变与更严重的疾病进程、更明显的炎症程度和更高频率的关节外病变相关。心肌功能状态综合指标与心电图数据的差异有统计学意义(p = 0.00001)。结论:第四代心电图显示,两种或两种以上促炎细胞因子不同基因突变的幼年特发性关节炎患者炎症过程活性更高,心血管改变频率更高。多态性的测定可能有助于评估心血管系统异常发展的风险。
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来源期刊
CiteScore
0.50
自引率
0.00%
发文量
33
审稿时长
20 weeks
期刊介绍: PEDIATRIA I MEDYCYNA RODZINNA is a peer-reviewed scientific journal publishing original articles that constitute significant contributions to the advancements of paediatrics and family medicine. In addition, PEDIATRIA I MEDYCYNA RODZINNA, publishes information from the medical associations, reports and materials from international congresses, letters to the Editor, information on new medical products as well as abstracts and discussions on papers published in other scientific journals, reviews of books and other publications.
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