Mavrogeni Sophie, Giannakopoulou Aikaterini, Papavasiliou Antigoni, Markousis-Mavrogenis George, Pons Roser, Karanasios Evangelos, Noutsias Michel, Kolovou Genovefa, Papadopoulos George
Onassis Cardiac Surgery Center, 50 Esperou Street, 175-61 P.Faliro, Athens, Greece.
Aghia Sophia Children's Hospital, Athens, Greece.
BMC Cardiovasc Disord. 2017 Jul 24;17(1):197. doi: 10.1186/s12872-017-0627-x.
To evaluate cardiovascular function in boys with Duchenne (DMD) and Becker (BMD) muscular dystrophy, using cardiac magnetic resonance (CMR).
This is a single point cross sectional study of twenty-four boys with genetically ascertained DMD, and 10 with BMD, aged 10.5 ± 1.5 years (range 9-13), were prospectively evaluated by a 1.5 T system and compared with those of age-sex matched controls. The DMD patients were divided in 2 groups. Group A (N = 12) were under treatment with both deflazacort and perindopril, while Group B (n = 12) were under treatment with deflazacort, only. BMD patients did not take any medication. Biventricular function was assessed using a standard SSFP sequence. Late gadolinium enhancement (LGE) was assessed from T1 images taken 15 min after injection of 0.2 mg/Kg gadolinium DTPA using a 3D-T1-TFE sequence.
Group A and BMDs were asymptomatic with normal ECG, 24 h ECG recording and echocardiogram. Group B were asymptomatic but 6/12 had abnormal ECG and mildly impaired LVEF. Their 24 h ECG recording revealed supraventricular and ventricular extrasystoles (all at 12-13 yrs). LV indices in Group A and BMD did not differ from those of controls. However, LV indices in Group B were significantly impaired compared with controls, Group A and BMDs (p < 0.001). An epicardial LGE area = 3 ± 0.5% of LV mass was identified in the posterolateral wall of LV only in 6/12 patients of Group B, but in not in any BMD or Group A.
Children with either BMD or DMD under treatment with both deflazacort and perindopril present preserved LV function and lack of LGE. However, further large scale multicenter studies are warranted to confirm these data, including further CMR mapping approaches.
使用心脏磁共振成像(CMR)评估杜氏(DMD)和贝克氏(BMD)肌营养不良男孩的心血管功能。
这是一项单点横断面研究,对24名经基因确诊的DMD男孩和10名BMD男孩进行前瞻性评估,这些男孩年龄为10.5±1.5岁(范围9 - 13岁),通过1.5T系统进行评估,并与年龄和性别匹配的对照组进行比较。DMD患者分为两组。A组(N = 12)接受地夫可特和培哚普利治疗,而B组(n = 12)仅接受地夫可特治疗。BMD患者未服用任何药物。使用标准稳态自由进动序列评估双心室功能。使用三维T1加权快速场回波序列,在注射0.2mg/kg钆喷酸葡胺15分钟后采集T1图像,评估延迟钆增强(LGE)。
A组和BMD组患者无症状,心电图、24小时心电图记录和超声心动图均正常。B组患者无症状,但12例中有6例心电图异常,左心室射血分数轻度受损。他们的24小时心电图记录显示有室上性和室性期前收缩(均在12 - 13岁时出现)。A组和BMD组的左心室指标与对照组无差异。然而,B组的左心室指标与对照组、A组和BMD组相比显著受损(p < 0.001)。仅在B组的12例患者中有6例在左心室后外侧壁发现心外膜LGE面积为左心室质量的3±0.5%,而BMD组和A组均未发现。
接受地夫可特和培哚普利治疗的BMD或DMD儿童左心室功能保留且无LGE。然而,需要进一步的大规模多中心研究来证实这些数据,包括进一步的CMR成像方法。