Structural features of the heart in children with arrhythmic syndrome due to nonspecific connective tissue disorder

Q4 Medicine
G. I. Nechaeva, A. N. Dakuko, E. N. Loginova, I. V. Bogatyrev
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Abstract

Introduction. Connective tissue is highly organized system, its disorders are characterized by a pronounced polymorphism of morphological and clinical manifestations. The cardiovascular pathology in patients with nonspecific connective tissue disorder attracts attention due to the high risk of complications: rhythm and conduction disorders, infective endocarditis, vascular thromboembolism and sudden cardiac death. Therefore, it’s very important to use up-to-date equipment and methods of early diagnosis of a high risk of fatal events in young. Aim. To investigate the structural features of the heart and their relationship with the process of myocardial remodeling in children with arrhythmic syndrome and nonspecific connective tissue disorder. Materials and methods. Sixty-five children were examined, 40 of them had arrhythmic syndrome in combination with nonspecific connective tissue disorder, and 25 had only minimal manifestations of nonspecific connective tissue disorder without arrhythmic syndrome. Such up-to-date methods as assessment of myocardial remodeling and longitudinal strain, natriuretic peptide assessment were included in the diagnostic algorithm. Results and discussion. The study showed a variety of phenotypic and visceral markers of nonspecific connective tissue disorder in children with arrhythmic syndrome. Arrhythmic syndrome was manifested by monotopic and heterotopic heart rhythm disorders, and structural changes of the heart: mitral valve prolapse and myocardial wall thinning were correlated with a more frequent increase in natriuretic peptide. Speckle-tracking echocardiography showed a significant decrease in longitudinal myocardial strain with predominance of myocardial strain in the anterior basal segment in children with arrhythmic syndrome. Conclusion. Our study showed a variety of phenotypic and visceral markers of undifferentiated connective tissue dysplasia in children with arrhythmic syndrome. The data obtained require further mathematical analysis and the establishment of a possible relationship between the external manifestations of the disease and cardiac rhythm and conduction disturbances.
非特异性结缔组织紊乱所致心律失常综合征患儿心脏结构特征
介绍。结缔组织是一个高度组织化的系统,其疾病具有明显的形态学和临床表现的多态性。非特异性结缔组织疾病患者的心血管病理引起了人们的关注,因为其并发症的风险很高:节律和传导障碍、感染性心内膜炎、血管血栓栓塞和心源性猝死。因此,使用最新的设备和方法对年轻人高风险的致命事件进行早期诊断非常重要。的目标。目的探讨心律失常综合征合并非特异性结缔组织疾病患儿心脏结构特征及其与心肌重构过程的关系。材料和方法。65名儿童接受了检查,其中40名患有心律失常综合征合并非特异性结缔组织疾病,25名只有轻微的非特异性结缔组织疾病表现,无心律失常综合征。诊断方法包括心肌重构和纵应变评估、利钠肽评估等最新方法。结果和讨论。该研究显示了心律失常综合征儿童非特异性结缔组织疾病的多种表型和内脏标志物。心律失常综合征表现为单位和异位心律失常,心脏结构改变:二尖瓣脱垂和心肌壁变薄与利钠肽升高更为频繁相关。斑点跟踪超声心动图显示,心律不齐综合征患儿纵向心肌应变明显减少,且以前基段心肌应变为主。结论。我们的研究显示了心律失常综合征儿童未分化结缔组织发育不良的各种表型和内脏标记物。获得的数据需要进一步的数学分析,并建立疾病的外部表现与心律和传导障碍之间的可能关系。
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来源期刊
Meditsinskiy Sovet
Meditsinskiy Sovet Medicine-Medicine (all)
CiteScore
0.70
自引率
0.00%
发文量
418
审稿时长
6 weeks
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