Prognostic value of humoral markers in patients with anthracycline-related cardiac dysfunction

IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL
E. V. Grakova, K. V. Kopeva, S. N. Shilov, E. T. Bobyleva, E. N. Berezikova, V. V. Kalyuzhin, A. T. Teplyakov
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引用次数: 0

Abstract

Aim. To carry out a 12-month study on the prognostic role of humoral markers responsible for the main mechanisms of initiation of cardiotoxic myocardial damage (endothelin-1, soluble Fas-L, N-terminal pro-brain natriuretic peptide (NT-proBNP), tumor necrosis factor-α, interleukin (IL)-1β, matrix metalloproteinase (MMP)-2 and MMP9, soluble form of the ST2 protein (sST2), a tissue inhibitor of metalloproteinase-1, and tetranectin) in assessing the risk of progression of anthracycline-related left ventricular dysfunction. Materials and methods. The study included a total of 114 women aged 48.0 (46.0; 52.0) years without concomitant cardiovascular diseases and risk factors who received chemotherapy with anthracyclines in the past. The levels of serum biomarkers were determined using the enzyme immunoassay. Transthoracic echocardiography was performed at baseline and at 12 months of follow-up. Results. After 12 months of follow-up, all patients were retrospectively divided into 2 groups: group 1 (n = 54) included patients with an unfavorable course of anthracycline-related cardiac dysfunction (ARCD), group 2 (n = 60) encompassed patients with a favorable course of the disease. According to the ROC analysis, MMP-2 ≥ ≥ 338.8 pg / ml (sensitivity 57%, specificity 78%; AUC = 0.629; p = 0.025), MMP-9 ≥ 22.18 pg / ml (sensitivity 89%, specificity 87%; AUC = 0.886; p < 0.001), sST2 ≥ 32.4 ng / ml (sensitivity 64%, specificity 70.5%; AUC = 0.691; p = 0.002), and tetranectin ≤ 15.4 pg / ml (sensitivity 69%, specificity 72%; AUC = 0.764; p < 0.001) were identified as predictors of an adverse course of ARCD. When comparing ROC curves, it was found that the concentration of MMP-9 (p = 0.002) was the most significant predictor of the progression of ARCD. Conclusion. MMP-2 and -9, soluble ST2, and tetranectin can be considered as non-invasive markers for assessing the risk of ARCD progression. At the same time, an increased level of MMP-9 is the most significant predictor of ARCD progression.
体液标志物在蒽环类药物相关性心功能障碍患者中的预后价值
的目标。目的:开展一项为期12个月的研究,研究与心毒性心肌损伤起始主要机制有关的血浆标志物(内皮素-1、可溶性Fas-L、n端前脑利钠肽(NT-proBNP)、肿瘤坏死因子-α、白细胞介素(IL)-1β、基质金属蛋白酶(MMP)-2和MMP9、可溶性ST2蛋白(sST2)、金属蛋白酶-1的组织抑制剂)的预后作用。评估蒽环类药物相关左心室功能障碍进展的风险。材料和方法。该研究共纳入114名年龄为48.0岁(46.0;52.0)岁,既往接受蒽环类药物化疗,无合并心血管疾病及危险因素。采用酶免疫分析法测定血清生物标志物水平。在基线和随访12个月时进行经胸超声心动图检查。结果。随访12个月后,所有患者回顾性分为2组:1组(n = 54)包括病程不良的蒽环类药物相关性心功能障碍(ARCD)患者,2组(n = 60)包括病程良好的患者。根据ROC分析,MMP-2≥≥338.8 pg / ml(敏感性57%,特异性78%;Auc = 0.629;p = 0.025), MMP-9≥22.18 pg / ml(敏感性89%,特异性87%;Auc = 0.886;p & lt;0.001), sST2≥32.4 ng / ml(敏感性64%,特异性70.5%;Auc = 0.691;P = 0.002),四联素≤15.4 pg / ml(敏感性69%,特异性72%;Auc = 0.764;p & lt;0.001)被认为是ARCD不良病程的预测因子。比较ROC曲线发现,MMP-9的浓度(p = 0.002)是ARCD进展的最显著预测因子。结论。MMP-2和-9、可溶性ST2和tetranectin可被视为评估ARCD进展风险的非侵入性标志物。同时,MMP-9水平升高是ARCD进展的最重要预测因子。
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来源期刊
Byulleten Sibirskoy Meditsiny
Byulleten Sibirskoy Meditsiny MEDICINE, GENERAL & INTERNAL-
CiteScore
0.70
自引率
50.00%
发文量
102
审稿时长
8 weeks
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