SERPINA3对蒽环类药物治疗和心血管功能障碍的动态反应。

IF 3.2 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Hanne M Boen, Lobke L Pype, Konstantinos Papadimitriou, Sevilay Altintas, Laure-Anne Teuwen, Sébastien Anguille, Kirsten Saevels, Anke Verlinden, Leen Delrue, Ward A Heggermont, Matthias Bosman, Pieter-Jan Guns, Hein Heidbuchel, Caroline M Van De Heyning, Emeline M Van Craenenbroeck, Constantijn Franssen
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引用次数: 0

摘要

背景:SERPINA3最近被认为是心力衰竭的潜在预后生物标志物。在患有癌症治疗相关性心功能障碍(CTRCD)的癌症幸存者人群中,与年龄匹配的对照组相比,循环SERPINA3升高。我们旨在评估接受蒽环类化疗(AnC)的癌症患者循环SERPINA3水平的纵向动态及其与CTRCD的关系。方法:在这项单中心队列研究中,前瞻性纳入了55例计划行AnC的癌症患者。在化疗前、化疗结束后、化疗结束后3个月和12个月进行心脏评价(超声心动图、高敏心肌肌钙蛋白I和NT-proBNP),并评估血浆SERPINA3水平。结果:55例患者中42例(76.4%)在治疗结束后1年内发生CTRCD。32例CTRCD患者为轻度,10例为中度,定义为心脏生物标志物或GLS和LVEF下降的变化。结论:循环SERPINA3水平在癌症患者群体中呈现动态变化,AnC后整体下降。然而,在中度CTRCD患者中,SERPINA3水平仍然升高。SERPINA3动态作为CTRCD生物标志物的潜力值得在更大的队列中验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dynamics of SERPINA3 in response to anthracycline treatment and cardiovascular dysfunction.

Dynamics of SERPINA3 in response to anthracycline treatment and cardiovascular dysfunction.

Dynamics of SERPINA3 in response to anthracycline treatment and cardiovascular dysfunction.

Dynamics of SERPINA3 in response to anthracycline treatment and cardiovascular dysfunction.

Background: SERPINA3 recently emerged as potential prognostic biomarker in heart failure. In a population of cancer survivors with cancer therapy-related cardiac dysfunction (CTRCD) circulating SERPINA3 was elevated compared to age-matched controls. We aimed to assess the longitudinal dynamics of circulating SERPINA3 levels in patients with cancer treated with anthracycline chemotherapy (AnC) and its relation to CTRCD.

Methods: In this single centre cohort study, 55 patients with cancer scheduled for AnC were prospectively enrolled. Cardiac evaluation (echocardiography, high-sensitive cardiac troponin I and NT-proBNP) was performed and SERPINA3 levels in plasma were assessed at 4 timepoints: before chemotherapy, directly after the end of chemotherapy, three months and twelve months after the end of chemotherapy.

Results: Forty-two out of 55 patients (76.4%) developed CTRCD within 1 year after end of treatment. CTRCD was mild in 32 and moderate in 10 patients, defined as a change in cardiac biomarkers or GLS and LVEF decline < 50% respectively. Overall, median SERPINA3 levels decreased from baseline to three months after AnC (215.7 [62.0-984.0] to 176.9 [94.7-678.0] µg/ml, p = 0.031). This decrease was most prominent in patients without CTRCD (30.8% decrease, p = 0.007), followed by mild CTRCD (9.0% decrease, p = 0.022), while patients with moderate CTRCD did not show a reduction in SERPINA3 (5.1% increase, p = 0.987). SERPINA3 values at three months after AnC were positively correlated with NT-proBNP (r = 0.47, p = 0.002). Several malignancy, treatment and patient characteristics were associated with higher SERPINA3 values.

Conclusion: Circulating SERPINA3 levels show dynamic changes in a population of patients with cancer, with an overall decrease following AnC. However, in patients that developed moderate CTRCD, SERPINA3 levels remained elevated. The potential of SERPINA3 dynamics as a biomarker for CTRCD, deserves validation in larger cohorts.

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来源期刊
Cardio-oncology
Cardio-oncology Medicine-Cardiology and Cardiovascular Medicine
CiteScore
5.00
自引率
3.00%
发文量
17
审稿时长
7 weeks
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