Faculty of Health Science, University of Sydney, Lidcombe, NSW, Australia.
Eur Heart J Cardiovasc Imaging. 2013 Mar;14(3):228-34. doi: 10.1093/ehjci/jes139. Epub 2012 Jul 10.
The benefits from anthracycline chemotherapy are undermined by potentially life-threatening cardiotoxicity. Transthoracic echocardiography is the most commonly used method for monitoring cardiotoxicity, and centres on the measurement of left ventricular systolic function. The aim of this study was to utilize two-dimensional speckle tracking echocardiography (2DSTE) at baseline and immediately after anthracycline chemotherapy to investigate whether patients with significant changes in systolic function after anthracycline therapy would also develop alterations in diastolic parameters.
Fifty-two women with histologically confirmed breast cancer were prospectively recruited. Echocardiograms were performed 1 week prior to and 1 week following chemotherapy (always before adjuvant trastuzumab or thoracic radiotherapy). Conventional Doppler, tissue velocity imaging (TVI), and 2DSTE were used to measure diastolic function. 2DSTE measurements included longitudinal diastolic strain, early (E-Sr), and late (A-Sr) myocardial strain rate. 2DSTE and left ventricular ejection fraction (LVEF) were used to measure longitudinal systolic function. Altered LV diastolic function (including E-Sr) was observed in the entire cohort after chemotherapy, with a differential reduction in participants with a post therapy LVEF <55%. Pre-chemotherapy systolic strain was found to predict reduced E-Sr post therapy (P = 0.04). Univariate predictors of E-Sr were LVEF post therapy (P = 0.049) and systolic strain post-therapy (P = 0.01). In a multivariate analysis, systolic strain after chemotherapy was the strongest independent predictor (P = 0.001).
Altered LV diastolic function was observed immediately after the administration of therapeutic doses of anthracycline chemotherapy. Furthermore, our analysis indicates that the changes in diastolic function are associated with reduced systolic function.
蒽环类化疗的益处因潜在危及生命的心脏毒性而受到损害。经胸超声心动图是监测心脏毒性最常用的方法,主要集中在左心室收缩功能的测量上。本研究的目的是利用二维斑点追踪超声心动图(2DSTE)在基线和蒽环类化疗后即刻测量,以调查在蒽环类治疗后收缩功能有显著变化的患者是否也会出现舒张参数的改变。
前瞻性招募了 52 名经组织学证实的乳腺癌女性患者。在化疗前 1 周和化疗后 1 周进行超声心动图检查(始终在辅助曲妥珠单抗或胸部放疗之前)。常规多普勒、组织速度成像(TVI)和 2DSTE 用于测量舒张功能。2DSTE 测量包括纵向舒张应变、早期(E-Sr)和晚期(A-Sr)心肌应变率。2DSTE 和左心室射血分数(LVEF)用于测量纵向收缩功能。整个队列在化疗后均观察到 LV 舒张功能改变(包括 E-Sr),在治疗后 LVEF <55%的参与者中差异更为明显。化疗前收缩应变被发现可预测治疗后 E-Sr 降低(P = 0.04)。E-Sr 的单变量预测因子包括治疗后 LVEF(P = 0.049)和治疗后收缩应变(P = 0.01)。在多变量分析中,化疗后收缩应变是最强的独立预测因子(P = 0.001)。
在给予治疗剂量的蒽环类化疗后,立即观察到 LV 舒张功能改变。此外,我们的分析表明舒张功能的变化与收缩功能降低有关。