Plasma branched-chain amino acid concentrations in individuals without cardiovascular diseases versus patients diagnosed with hypertension and coronary artery disease

IF 0.3 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
M. Kozhevnikova, E. O. Korobkova, A. V. Krivova, A. Kukharenko, N. Moskaleva, K. Shestakova, N. Mesonzhnik, A. Ageev, A. A. Boldin, A. Brito, S. Appolonova, E. Privalova, Y. Belenkov
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引用次数: 0

Abstract

Aim. Branched-chain amino acids (BCAAs) have been postulated as potential indicators of cardiovascular risk. The objective of this study was to explore the relationship between plasma BCAAs and different stages of cardiovascular disorders.Material and methods. In our cross-sectional study, plasma BCAAs (valine, leucine and isoleucine) in individuals without cardiovascular diseases (CVDs) (nonCVD group, total n=27, with n=16 healthy, but with metabolic disorders) were compared to patients diagnosed with CVDs [CVD group, total n=109, being n=61 hypertension (n=31 with signs of beginning of myocardial remodeling) and n=48 patients with coronary artery disease (CAD)].Results. The plasma concentration of BCAAs was significantly higher in the group of patients with cardiovascular disease compared with the healthy group (p<0.05 for all amino acids tested): valine concentration was 238.7 [219.6; 267.0] μM in the non-CVD group and 261.2 [233.8; 298.7] μM in the CVD group; leucine concentration was 134.8 [122.4; 153.2] μM and 146.8 [129.0; 166.6] μM, respectively; and isoleucine 72.7 [65.3; 84.4] μM and 81.7 [68.0; 96.2] μM, respectively. Leucine and isoleucine concentration levels were minimal in the healthy participant subgroup and maximal in the IBS patient subgroup. No statistically significant differences in BCAAs concentrations were found in the subgroups without CAD. Significant increases in concentrations were observed in the subgroups of patients with CAD as follows: valine concentration was 256.3 [219.0; 297.9] μM in hypertension group and 261.7 [236.5; 307.5] μM in CAD group; leucine concentration was 141.8 [123.5; 166.6] μM and 154.1 [134.7; 172.7] μM, respectively, and isoleucine 72.8 [65.7; 94.0] μM and 85.7 [74.9; 101.7] μM, respectively. BCAAs profiles in all participants with metabolic disorders had “good” diagnostic accuracy with area under the receiver operating characteristics curve being 0.72, 0.70 and 0.70 for valine, leucine and isoleucine, respectively.Conclusion. BCAAs concentrations are elevated with higher severity of the cardiovascular disorder and exhibit potential as early independent indicators of coronary artery disease.
无心血管疾病个体与诊断为高血压和冠状动脉疾病患者的血浆支链氨基酸浓度
的目标。支链氨基酸(BCAAs)被认为是心血管风险的潜在指标。本研究的目的是探讨血浆支链氨基酸与不同阶段心血管疾病的关系。材料和方法。在我们的横断面研究中,将无心血管疾病(CVD)个体(非CVD组,总n=27,健康但有代谢障碍的n=16)的血浆BCAAs(缬氨酸、亮氨酸和异亮氨酸)与诊断为CVD的患者(CVD组,总n=109,其中n=61高血压(n=31有心肌重构开始的体征)和n=48有冠状动脉疾病(CAD)的患者)进行比较。结果。心血管疾病患者血浆BCAAs浓度显著高于健康组(各氨基酸检测值p<0.05):缬氨酸浓度为238.7 [219.6;非cvd组267.0]m, 261.2 [233.8] m;298.7] μM在CVD组;亮氨酸浓度为134.8 [122.4;153.2] μM和146.8 [129.0;166.6] μM;异亮氨酸72.7 [65.3;84.4] μM和81.7 [68.0];96.2] μM。亮氨酸和异亮氨酸浓度水平在健康参与者亚组中最低,在肠易激综合征患者亚组中最高。在没有CAD的亚组中,BCAAs浓度无统计学差异。在CAD患者亚组中观察到的浓度显著升高如下:缬氨酸浓度为256.3 [219.0;高血压组297.9 μM, 261.7 μM [236.5];307.5] μM CAD组;亮氨酸浓度为141.8 [123.5;166.6] μM和154.1 [134.7];172.7] μM,异亮氨酸72.8 [65.7;94.0] μM和85.7 [74.9];101.7] μM。所有代谢紊乱患者的BCAAs谱具有“良好”的诊断准确性,缬氨酸、亮氨酸和异亮氨酸的受试者工作特征曲线下面积分别为0.72、0.70和0.70。BCAAs浓度随着心血管疾病严重程度的升高而升高,并表现出作为冠状动脉疾病早期独立指标的潜力。
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来源期刊
Rational Pharmacotherapy in Cardiology
Rational Pharmacotherapy in Cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
1.00
自引率
50.00%
发文量
79
审稿时长
6 weeks
期刊介绍: The primary goals of the Journal are consolidation of information on scientific and practical achievements in pharmacotherapy and prevention of cardiovascular diseases and continuing education of cardiologists and internists. The scientific concept of the edition suggests the publication of information on current achievements in cardiology, the results of national and international clinical trials. The Journal publishes original articles on the results of clinical trials designed to study the effectiveness and safety of drugs, analysis of clinical practice and its compliance with national and international recommendations, expert s’ opinions on a wide range of cardiology issues, associated conditions and clinical pharmacology. There is a heading “Preventive cardiology and public health” in the Journal to stimulate research interest in this highly demanded area. Memories of the outstanding people in medicine including cardiology, which are of great interest to historians of medicine, are published in "Our Mentors” heading.
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