Migrino Raymond Q, Aggarwal Deepika, Konorev Eugene, Brahmbhatt Tejas, Bright Megan, Kalyanaraman Balaraman
Cardiovascular Division, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Ultrasound Med Biol. 2008 Feb;34(2):208-14. doi: 10.1016/j.ultrasmedbio.2007.07.018. Epub 2007 Oct 23.
Doxorubicin is one of the most effective chemotherapeutic agents; however, it causes dose-dependent cardiomyopathy that may lead to heart failure. Conventional measures of ventricular function, such as fractional shortening, are insensitive in detecting early doxorubicin cardiomyopathy. We tested whether novel two-dimensional radial strain echocardiography (2DSE) can detect early doxorubicin injury following chronic administration in a rat model. 14 male Sprague Dawley rats (240 to 260 g) received doxorubicin 2.5 mg/k i.v. per wk for 10 (n=4) or 12 wk (n=10); 17 controls received saline (10 wk, n=7 and 12 wk, n=10). Serial 2DSE from 0 to 12 wk was done at the mid left ventricle using Vivid 7 echo (General Electric, Waukesha, WI, USA). With Q analysis software, radial strain was obtained. From the two-dimensional (2D) image, anatomical M-mode through the anterior/inferior walls was used to measure fractional shortening. Fibrosis (Masson's trichrome) and caspase-3 activity were measured from excised hearts. Radial strain was lower in the doxorubicin group (12 wk: 26.7+/-3 versus 38.3+/-2.6%, p=0.006), with significant difference by 8 wk whereas fractional shortening was lower with doxorubicin only after 12 wk (30.2+/-1.7 versus 37.6+/-1.4%, p=0.02). Doxorubicin group had lower cardiac mass (0.85+/-0.09 versus 1.14+/-0.04 g, p=0.001), higher caspase-3 activity (1.95+/-0.2 fold increase over control, p<0.0001) and fibrosis (3.9 +/- 0.7 versus 0.7+/-0.1%, p=0.005). Radial strain was related directly to cardiac mass (r=0.61, p=0.0007) and inversely to caspase-3 activity (r= -0.5, p=0.005). 2-dimensional radial strain echocardiography is useful in the early detection of doxorubicin cardiac injury and the reduction in radial strain is associated with histologic markers of doxorubicin cardiomyopathy.
阿霉素是最有效的化疗药物之一;然而,它会引发剂量依赖性心肌病,进而可能导致心力衰竭。传统的心室功能测量方法,如缩短分数,在检测早期阿霉素心肌病方面并不敏感。我们测试了新型二维径向应变超声心动图(2DSE)能否在大鼠模型中检测慢性给药后的早期阿霉素损伤。14只雄性斯普拉格-道利大鼠(体重240至260克)每周静脉注射阿霉素2.5毫克/千克,持续10周(n = 4)或12周(n = 10);17只对照大鼠接受生理盐水注射(10周,n = 7;12周,n = 10)。使用Vivid 7超声(美国威斯康星州沃基沙的通用电气公司)在左心室中部从0至12周进行连续二维超声心动图检查。通过Q分析软件获取径向应变。从二维(2D)图像中,利用穿过前壁/下壁的解剖M型超声来测量缩短分数。从切除的心脏中测量纤维化(Masson三色染色法)和半胱天冬酶-3活性。阿霉素组的径向应变较低(12周时:26.7±3% 对 38.3±2.6%,p = 0.006),在8周时就有显著差异,而缩短分数仅在12周后阿霉素组才降低(30.2±1.7% 对 37.6±1.4%,p = 0.02)。阿霉素组的心脏重量较低(0.85±0.09克 对 1.14±0.04克,p = 0.001),半胱天冬酶-3活性较高(比对照组增加1.95±0.2倍,p < 0.0001)以及纤维化程度较高(3.9±0.7% 对 0.7±0.1%,p = 0.005)。径向应变与心脏重量直接相关(r = 0.61,p = 0.0007),与半胱天冬酶-3活性呈负相关(r = -0.5,p = 0.005)。二维径向应变超声心动图有助于早期检测阿霉素引起的心脏损伤,径向应变的降低与阿霉素心肌病的组织学标志物相关。