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血清N末端脑钠肽前体早期诊断蒽环类药物心脏毒性的实验研究
引用本文:赖仁纯,卢雅立,苏晓东,郭晋,蒋愈,戎铁华.血清N末端脑钠肽前体早期诊断蒽环类药物心脏毒性的实验研究[J].岭南急诊医学杂志,2012,0(4):243-245,248.
作者姓名:赖仁纯  卢雅立  苏晓东  郭晋  蒋愈  戎铁华
作者单位:1. 华南肿瘤学国家重点实验室,中山大学肿瘤防治中心
2. 麻醉科510060
3. 胸外科
基金项目:广东省卫生厅医学科学基金(B2009088)
摘    要:目的:探讨血清N末端脑钠肽前体(NT-proBNP)浓度是否可成为蒽环类药物心脏毒性的早期诊断指标.方法:新西兰雄性兔44只随机分为对照组和实验组,对照组新西兰兔静脉注射等体积的生理盐水,实验组分为4组,每次给予阿霉素2 mg/kg,每周1次,根据给药周数不同,分为1周组、2周组、4周组和8周组.经胸超声心动图测量左室射血分数(LVEF)和左室短轴缩短分数(FS)以及E峰和A峰比率,血清NT-proBNP浓度测量采用酶联免疫吸附测定法(ELISA),心肌光镜Billingham评分和电镜检查评价蒽环类药物心脏毒性.结果:8周组新西兰兔LVEF、FS以及E/A比率均下降(P<0.05),4周组新西兰兔心肌病评分高于对照组、1周组和2周组(P<0.05).八周组新西兰兔心肌病评分高于其余各组新西兰兔(P<0.05).心肌电镜检查结果证实二周组、四周组和八周组新西兰兔心肌损伤.与对照组血清NT-proBNP浓度相比,二周组、四周组和八周组新西兰兔血清NT-proBNP浓度均明显上升(P<0.05).通过相关分析提示血清NT-proBNP浓度与阿霉素累积剂量及心肌损害的程度呈正相关.结论:血清NT-proBNP浓度可能是蒽环类药物心脏毒性较早期诊断指标.

关 键 词:N末端脑钠肽前体  心脏毒性  阿霉素  蒽环类药物

Serum NT-proBNP as a Marker for Early Detection for Anthracycline-induced Cardiotoxicity in Rabbits
LAI Ren-chun,LU Ya-li,SU Xiao-dong,GUO Jin,Jiang Yu,RONG Tie-Hua.Serum NT-proBNP as a Marker for Early Detection for Anthracycline-induced Cardiotoxicity in Rabbits[J].Lingnan Journal of Emergency Medicine,2012,0(4):243-245,248.
Authors:LAI Ren-chun  LU Ya-li  SU Xiao-dong  GUO Jin  Jiang Yu  RONG Tie-Hua
Institution:1.Department of A nesthesiology, State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, 510060 2.Department of Thoracic Surgery)
Abstract:Objective:To investigate serum NT-proBNP concentrations as an early biomarker for anthracycline-induced myocardial damage in rabbits. Methods: 44 male rabbits were randomly divided into control group or one of four doxorubicin groups. Rabbits in control group received saline, while rabbits in doxorubicin group received 2 mg/kg doxorubicin weekly for one (Group 1), two (Group 2), four (Group 3) and eight(Group 4)weeks. Echocardiography was performed to measure left ventricular ejection fraction (LVEF), fractional shortening (FS), and E/A ratio. Serum NT-proBNP concentrations were quantified by a rabbit-specific enzyme-linked immunosorbent assay (ELISA). Cardiotoxicity scores were determined by light microscopy using Billingham's method and by electron microscopy. Results: Decreased LVEF, FS, and E/A ratio were detected in Group 4 (P 〈 0.05). The Billingham cardiomyopathy scores of the rabbits in Group 3 were significantly higher (P 〈 0.05) than those of rabbits in control group or Groups 1 or 2. The Billingham cardiomyopathy scores in Group 4 were the highest of all five groups (P 〈 0.05). Myocardial injury was verified by electron microscopy in rabbits from Groups 2, 3, and 4. Compared with control group, serum NT-proBNP concentrations increased in Groups 2, 3, and 4 (P 〈 0.05). A positive correlation between the serum NT- proBNP concentrations and both the dose of doxorubicin and the cardiomyopathy score was found. Conclusion: Serum NT-proBNP concentrations may be a sensitive method for assessing early cardiotoxicity induced by anthracycline.
Keywords:NT-proBNP  cardiotoxicity  Doxorubicin  Anthracycline
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