Hor Kan N, Wansapura Janaka, Markham Larry W, Mazur Wojciech, Cripe Linda H, Fleck Robert, Benson D Woodrow, Gottliebson William M
Department of Cardiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229-3039, USA.
J Am Coll Cardiol. 2009 Apr 7;53(14):1204-10. doi: 10.1016/j.jacc.2008.12.032.
This study sought to evaluate the natural history of occult cardiac dysfunction in Duchenne muscular dystrophy (DMD).
Duchenne muscular dystrophy is characterized by progressive cardiac dysfunction and myocardial fibrosis late in the disease process. We hypothesized that left ventricular myocardial peak circumferential strain (epsilon(cc)) would decrease in DMD before global systolic functional abnormalities regardless of age or ventricular ejection fraction (EF).
We evaluated cardiac magnetic resonance image (MRI) data from 70 DMD patients and 16 aged-matched control subjects. Standard imaging data included steady-state free precession short-axis cine stack images, cine myocardial tagged images, and myocardial delayed enhancement (MDE) (an indicator of myocardial fibrosis) sequences. Analysis was performed with QMASS (Medis Medical Imaging Systems, Leiden, the Netherlands) and HARP (Diagnosoft, Palo Alto, California) software. The DMD patient data were subdivided by age (<10 or >10 years), EF (>55% or <55%), and the presence or absence of MDE.
The DMD patients with normal EF had reduced epsilon(cc) at an early age (<10 years) compared with control subjects (p < 0.01). The DMD patients age >10 years with normal EF had further decline in epsilon(cc) compared with younger DMD patients (p < 0.01). There was further decline in epsilon(cc) with age in patients with reduced EF (p < 0.01) without MDE. The oldest patients, with both reduced EF and positive MDE, exhibited the lowest epsilon(cc). None of the patients had ventricular hypertrophy.
Myocardial strain abnormalities are prevalent in young DMD patients despite normal EF, and these strain values continue to decline with advancing age. Strain analysis in combination with standard MRI and MDE imaging provides a means to stratify DMD cardiomyopathy.
本研究旨在评估杜氏肌营养不良症(DMD)隐匿性心脏功能障碍的自然病史。
杜氏肌营养不良症的特征是在疾病后期出现进行性心脏功能障碍和心肌纤维化。我们假设,无论年龄或心室射血分数(EF)如何,在全球收缩功能异常之前,DMD患者的左心室心肌峰值圆周应变(ε(cc))会降低。
我们评估了70例DMD患者和16例年龄匹配的对照受试者的心脏磁共振成像(MRI)数据。标准成像数据包括稳态自由进动短轴电影堆栈图像、电影心肌标记图像和心肌延迟强化(MDE)(心肌纤维化指标)序列。使用QMASS(Medis Medical Imaging Systems,荷兰莱顿)和HARP(Diagnosoft,加利福尼亚州帕洛阿尔托)软件进行分析。DMD患者数据按年龄(<10岁或>10岁)、EF(>55%或<55%)以及是否存在MDE进行细分。
与对照受试者相比,EF正常的DMD患者在早年(<10岁)时ε(cc)降低(p<0.01)。与年轻的DMD患者相比,年龄>10岁且EF正常的DMD患者的ε(cc)进一步下降(p<0.01)。EF降低且无MDE的患者中,ε(cc)随年龄进一步下降(p<0.01)。年龄最大且EF降低和MDE阳性的患者表现出最低的ε(cc)。所有患者均无心室肥厚。
尽管EF正常,但年轻DMD患者中普遍存在心肌应变异常,且这些应变值随年龄增长持续下降。应变分析与标准MRI和MDE成像相结合为DMD心肌病分层提供了一种方法。