慢性心力衰竭患者游离循环DNA水平、射血分数和脑利钠肽水平的关系:前瞻性观察研究

Q4 Medicine KardioSomatika Pub Date : 2023-11-06 DOI:10.17816/cs456434
Elena V. Kolesnikova, Olga V. Myachina, Alexander N. Pashkov
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 MATERIALS AND METHODS: The study involved 67 patients of both sexes with a diagnosis of CHF, verified by clinical and functional methods. 23 people without established chronic diseases formed the control group. At the stage of inclusion in the study, all patients underwent: physical examination, general blood test, biochemical blood test with determination of lipid profile, glucose, creatinine, NT-proBNP and cfDNA levels, as well as electrocardiography (ECG), electrocardiography (ECHO-CG), radiography of organs chest, ultrasound of the abdominal organs, 6-minute walk test. The level of cfDNA was determined using the method of P.P. Laktionov, S.N. Tamkovich, E.Yu. Rykova (2005). Repeated blood sampling with assessment of cfDNA and NT-proBNP levels was carried out in the group of patients with reduced ejection fraction 57 months from the start of treatment/correction of previous therapy.
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引用次数: 0

摘要

背景:慢性心力衰竭(CHF)是心血管疾病中最严重的问题之一,需要准确的诊断和治疗。寻找新的CHF实验室标志物可以提高诊断的准确性和识别患者病情的严重程度。 目的:研究伴有射血分数(EF)的CHF患者血浆中游离循环DNA (cfDNA)水平与脑利钠肽(NT-proBNP)水平的关系,探讨这些实验室标志物之间的关系,并在药物治疗背景下评价所研究参数的变化动态。材料和方法:本研究纳入67例诊断为CHF的男女患者,经临床和功能方法验证。无慢性疾病的23人作为对照组。在纳入研究阶段,所有患者均接受:体格检查、血液常规检查、血液生化检查(包括血脂、血糖、肌酐、NT-proBNP和cfDNA水平),以及心电图(ECG)、心电图(回声心动图)、脏器胸部x线片、腹部脏器超声、6分钟步行试验。采用P.P. Laktionov, S.N. Tamkovich, e.o yu的方法测定cfDNA水平。Rykova(2005)。在开始治疗/纠正先前治疗的57个月后,对射血分数降低的患者进行反复采血,评估cfDNA和NT-proBNP水平。结果:研究显示不同EF患者血浆cfDNA水平(小于40%、4049%、50%或更高)存在显著差异。同时,cfDNA指标与EF、NT-proBNP水平与EF呈反比关系,即心肌收缩力的逐渐下降伴随着血液中所研究的标志物水平的联合升高,反映了患者病情的严重程度。此外,已证实药物治疗对EF 40%患者组cfDNA和NT-proBNP水平有积极作用。 结论:所鉴定的模式使得血浆中cfDNA水平可以作为CHF的潜在生物标志物,并可用于患者的动态监测。
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Relationship between free circulating DNA levels, ejection fraction and brain natriuretic peptide levels in patients with chronic heart failure: prospective observational study
BACKGROUND: Chronic heart failure (CHF) is one of the most serious problems in cardiovascular diseases, requiring accurate diagnosis and treatment. The search for new laboratory markers of CHF can improve the accuracy of diagnosis and identify the severity of the patients condition. AIM: Our aim was to study the relationship between the levels of free-circulating DNA (cfDNA) and brain natriuretic peptide (NT-proBNP) in the blood plasma of patients suffering from CHF with ejection fraction (EF), to investigate the relationship between these laboratory markers, and to evaluate the dynamics of changes in the studied parameters against the background of drug therapy. MATERIALS AND METHODS: The study involved 67 patients of both sexes with a diagnosis of CHF, verified by clinical and functional methods. 23 people without established chronic diseases formed the control group. At the stage of inclusion in the study, all patients underwent: physical examination, general blood test, biochemical blood test with determination of lipid profile, glucose, creatinine, NT-proBNP and cfDNA levels, as well as electrocardiography (ECG), electrocardiography (ECHO-CG), radiography of organs chest, ultrasound of the abdominal organs, 6-minute walk test. The level of cfDNA was determined using the method of P.P. Laktionov, S.N. Tamkovich, E.Yu. Rykova (2005). Repeated blood sampling with assessment of cfDNA and NT-proBNP levels was carried out in the group of patients with reduced ejection fraction 57 months from the start of treatment/correction of previous therapy. RESULTS: The study revealed significant differences in the levels of cfDNA in the blood plasma in patients with different EF (less than 40%, 4049%, 50% or more). At the same time, an inverse relationship was established between cfDNA indicators and EF, as well as between the level of NT-proBNP and EF, that is, a progressive decrease in myocardial contractility is accompanied by a combined increase in the levels of the studied markers in the blood, reflecting the severity of the patients condition. In addition, the positive effect of drug therapy on cfDNA and NT-proBNP levels in the group of patients with EF 40% has been proven. CONCLUSION: The identified patterns make it possible to consider the level of cfDNA in blood plasma as a potential biomarker of CHF, and also to use it for dynamic monitoring of patients.
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CiteScore
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11
审稿时长
6 weeks
期刊最新文献
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