Pattoneri Paolo, Pelà Giovanna, Montanari Enrico, Pesci Ilaria, Moruzzi Paolo, Montanari Alberto
Operative Unit of Cardiology, Hospital of Fidenza/San Secondo, Azienda USL di Parma, Parma, Italy.
Department of Clinical Sciences, University of Parma, Parma, Italy.
Heart Asia. 2012 Jan 1;4(1):91-4. doi: 10.1136/heartasia-2012-010117. eCollection 2012.
The authors sought to investigate the ability of the Doppler-derived myocardial performance index (MPI) to predict cardiotoxicity in multiple sclerosis (MS) patients under mitoxantrone therapy.
The aauthors prospectively evaluated 28 MS patients (mean age 41±9 years, 12 males and 16 females) treated with low-dose mitoxantrone (basal mean cumulative dose 30±14 mg/m(2), end of follow-up mean dose 41±17 mg/m(2)). All patients underwent two-dimensional and Doppler-echocardiography at baseline and after a mean follow-up of 22±8 months. MPI was estimated using mitral inflow and left ventricular (LV) outflow pattern. Comparing data at baseline and at the end of follow-up, significant decrease in ejection fraction (EF) was observed (60±5 vs 56±4, p<0.03). The MPI was 0.52±0.1 at baseline and 0.60±0.1 at the end of follow-up (p<0.04). Such difference was mainly due to a isovolumic relaxation time prolongation (80±12 at baseline and 98±30 at the end of follow-up, p<0.05). The area under the receiver operating characteristic curve, analysed for an MPI cut-point value of 0.57, in identifying a significant reduction of LVEF ≤50% was of 0.94±0.065 with sensitivity and specificity of 97.5% and 90%, respectively.
In conclusion, it can be speculated that a higher basal value of MPI could represent a subclinical LV cardiotoxicity, identifying a future decrease of EF and a progression to congestive heart failure in MS patients under mitoxantrone therapy.
作者试图研究多普勒衍生的心肌性能指数(MPI)预测接受米托蒽醌治疗的多发性硬化症(MS)患者心脏毒性的能力。
作者前瞻性评估了28例接受低剂量米托蒽醌治疗的MS患者(平均年龄41±9岁,男性12例,女性16例)(基础平均累积剂量30±14mg/m²,随访结束时平均剂量41±17mg/m²)。所有患者在基线时和平均随访22±8个月后接受二维和多普勒超声心动图检查。使用二尖瓣流入和左心室(LV)流出模式估计MPI。比较基线和随访结束时的数据,观察到射血分数(EF)显著降低(60±5对56±4,p<0.03)。MPI在基线时为0.52±0.1,随访结束时为0.60±0.1(p<0.04)。这种差异主要是由于等容舒张时间延长(基线时为80±12,随访结束时为98±30,p<0.05)。对于MPI切点值为0.57分析的受试者工作特征曲线下面积,在识别LVEF≤50%的显著降低方面为0.94±0.065,敏感性和特异性分别为97.5%和90%。
总之,可以推测较高的MPI基础值可能代表亚临床左心室心脏毒性,识别接受米托蒽醌治疗的MS患者未来EF的降低和充血性心力衰竭的进展。