Department of Cardiology, Erasme Hospital, Université Libre de Bruxelles, 808 Route de Lennik, Brussels, Belgium.
Eur Heart J Cardiovasc Imaging. 2012 Apr;13(4):346-52. doi: 10.1093/ejechocard/jer267. Epub 2011 Nov 28.
Myocardial involvement in Friedreich's ataxia (FRDA) is characterized by iron deposits, diffuse fibrosis, and focal necrosis. We hypothesized that subclinical left ventricular (LV) dysfunction may occur in 'FRDA patients who have normal LV ejection fraction (LVEF) and mass.
Twenty patients homozygous for the GAA expansion in the frataxin gene (mean age: 35 ± 16 years) and twenty age- and sex-matched controls (mean age: 34 ± 15 years) were studied using conventional echocardiography and speckle-tracking imaging. The two groups did not differ in terms of the LVEF (68 ± 6 vs. 67 ± 6%, in patients and controls, respectively) or LV mass (91 ± 20 vs. 82 ± 17 g/m(2)). Global systolic longitudinal (-15.3 ± 2.1 vs. -17.5 ± 1.6%, P = 0.001) and circumferential (-19.5 ± 2.9 vs. -21.4 ± 2.6%, P = 0.034) strain, and peak LV twist (9.2 ± 3.3 vs. 11.7 ± 2.3°, P = 0.008) were significantly reduced in patients compared with controls. Indexed stroke volume was also significantly lower in patients (36 ± 5 vs. 43 ± 8 mL/m(2), P = 0.0012) and this decreased LV pump performance was associated with a concentric remodelling pattern (relative wall thickness: 0.47 ± 0.08 vs. 0.35 ± 0.05, P < 0.001).
There is evidence of morphological and functional abnormalities in FRDA patients with normal LVEF and mass.
弗里德赖希共济失调(FRDA)的心肌受累表现为铁沉积、弥漫性纤维化和局灶性坏死。我们假设,在左心室射血分数(LVEF)和质量正常的 FRDA 患者中可能存在亚临床左心室(LV)功能障碍。
使用常规超声心动图和斑点追踪成像技术研究了 20 名 FRDA 基因 GAA 扩增纯合子患者(平均年龄:35 ± 16 岁)和 20 名年龄和性别匹配的对照组(平均年龄:34 ± 15 岁)。两组的 LVEF(分别为 68 ± 6%和 67 ± 6%)或 LV 质量(分别为 91 ± 20 g/m2和 82 ± 17 g/m2)均无差异。与对照组相比,患者的整体收缩纵向应变(-15.3 ± 2.1%对-17.5 ± 1.6%,P = 0.001)和环向应变(-19.5 ± 2.9%对-21.4 ± 2.6%,P = 0.034)以及 LV 扭转峰值(9.2 ± 3.3°对 11.7 ± 2.3°,P = 0.008)明显降低。患者的指数化每搏量也明显降低(36 ± 5 vs. 43 ± 8 mL/m2,P = 0.0012),这种降低的 LV 泵功能与向心性重构模式相关(相对壁厚度:0.47 ± 0.08 对 0.35 ± 0.05,P < 0.001)。
在 LVEF 和质量正常的 FRDA 患者中,存在形态和功能异常的证据。