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贝克型肌营养不良症中的亚临床心肌病。

Subclinical cardiomyopathy in Becker muscular dystrophy.

作者信息

Steare S E, Dubowitz V, Benatar A

机构信息

Department of Medicine (Cardiology), Hammersmith Hospital, London.

出版信息

Br Heart J. 1992 Sep;68(3):304-8. doi: 10.1136/hrt.68.9.304.

Abstract

OBJECTIVE

To investigate the prevalence, age distribution, and spectrum of cardiac involvement in a cohort of patients with Becker muscular dystrophy.

DESIGN

A prospective non-invasive study with clinical, electrocardiographic, and echocardiographic assessment.

PATIENTS

19 patients (age range 16-41 years) with Becker muscular dystrophy attending the Muscle Clinic at Hammersmith Hospital and 22 healthy controls (age range 22-36 years).

RESULTS

17 patients (89%) were symptom free; two had exertional dyspnoea. Three had a past history of acute pericarditis. The electrocardiogram was abnormal in 14 patients (74%). Intraventricular conduction delay or right bundle branch block was present in eight (42%). Three (16%) had tall R waves (R/S > 1) in lead V1 in the absence of right bundle branch block and eight (42%) had Q waves in the lateral and inferolateral leads. The PQ interval was significantly shorter in patients with Becker muscular dystrophy (p < 0.01). Echocardiography showed left ventricular dilatation in seven patients (37%) and 12 (63%) had subnormal systolic function caused by global hypokinesia (fractional shortening < 27%). Six of these patients were under the age of 22 years. Patients with Becker muscular dystrophy had significant reduction of both fractional shortening and corrected mean velocity of circumferential shortening compared with controls. No correlation was found between fractional shortening and age. The third filling fraction was significantly reduced in patients with Becker muscular dystrophy (p < 0.05), although other indices of diastolic function (isovolumic relaxation time and E/A ratios) were not significantly different.

CONCLUSIONS

Though most patients with Becker muscular dystrophy were symptom free, a high percentage had evidence of a subclinical cardiomyopathy. Electrocardiography showed that the inferolateral and posterior segments of the left ventricle tended to be affected and may show evidence for conduction tissue disease. Echocardiography showed that most patients had left ventricular dilation and global hypokinesia. The severity of left ventricular disease was unrelated to age; some younger patients had severe left ventricular dysfunction. All patients with Becker muscular dystrophy should have echocardiographic assessment of left ventricular function.

摘要

目的

调查一组贝克型肌营养不良患者心脏受累的患病率、年龄分布及范围。

设计

一项采用临床、心电图及超声心动图评估的前瞻性非侵入性研究。

患者

19例年龄在16至41岁之间的贝克型肌营养不良患者,就诊于哈默史密斯医院的肌肉诊所,以及22名健康对照者(年龄在22至36岁之间)。

结果

17例患者(89%)无症状;2例有劳力性呼吸困难。3例有急性心包炎病史。14例患者(74%)心电图异常。8例(42%)存在室内传导延迟或右束支传导阻滞。3例(16%)在无右束支传导阻滞的情况下V1导联R波高大(R/S>1),8例(42%)在侧壁和下侧壁导联有Q波。贝克型肌营养不良患者的PQ间期显著缩短(p<0.01)。超声心动图显示7例患者(37%)左心室扩张,12例(63%)因整体运动减弱(缩短分数<27%)出现收缩功能低于正常。其中6例患者年龄在22岁以下。与对照组相比,贝克型肌营养不良患者的缩短分数和校正平均圆周缩短速度均显著降低。未发现缩短分数与年龄之间存在相关性。贝克型肌营养不良患者的第三心音充盈分数显著降低(p<0.05),尽管舒张功能的其他指标(等容舒张时间和E/A比值)无显著差异。

结论

虽然大多数贝克型肌营养不良患者无症状,但很大比例有亚临床心肌病的证据。心电图显示左心室下侧壁和后壁段易受累,可能有传导组织疾病的证据。超声心动图显示大多数患者有左心室扩张和整体运动减弱。左心室疾病的严重程度与年龄无关;一些年轻患者有严重的左心室功能障碍。所有贝克型肌营养不良患者均应接受左心室功能的超声心动图评估。

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