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施泰纳特病的舒张功能

Diastolic Function in Steinert's Disease.

作者信息

Fayssoil Abdallah, Nardi Olivier, Annane Djillali, Orlikowski David

机构信息

Critical Care Unit, Raymond Poincaré Hospital, University of Versailles SQY , Garches, France.

出版信息

Neurol Int. 2014 Mar 31;6(1):5140. doi: 10.4081/ni.2014.5140. eCollection 2014 Jan 17.

Abstract

Myotonic dystrophy type 1 (MD) is the most common autosomal dominant muscular dystrophy in adults. Cardiac involvement is mainly characterized by conduction abnormalities and arrhythmias. We sought to assess diastolic function in MD patients. Echocardiography-Doppler was performed in Steinert's patients and in a control group completed by tissue Doppler imaging (TDI). Twenty-six patients with Steinert's disease were included in the study and were compared to a control group. Mean age was similar in the 2 groups (45.1 years ±10.9 in Steinert's patients vs 42.1 years ±11 in control group p 0.4). 6 /26 patients with Steinert's disease disclosed a left ventricular (LV) ejection fraction <50%. Mean left atrial (LA) diameter was statistically different between Steinert's patients and patients in group control (27.8 mm ±8.5 vs 19.7 mm ±4; P=0.0018). Mean peak E/A mitral ratio was 1.29±0.45 in Steinert's patients vs 1.36±0.4 in control group (P=0.6). We found an increase of the mitral E deceleration time in Steinert's patients in comparison with patients in control group (219 ms ±53 vs 176 ms ±29; P=0.013). Mean peak lateral early diastolic velocity Ea was similar in the 2 groups (12.3 cm/s ±3 vs 13.1 cm/s ±3.8; P=0.50). Mean peak septal early diastolic velocity was similar in the 2 groups (11.2 cm/s ±2 vs 10.4±2; P=0.51). We found an increase of the LA diameter and an increase of the mitral deceleration time in Steinert's patients that suggest diastolic abnormalities.

摘要

1型强直性肌营养不良(MD)是成人中最常见的常染色体显性遗传性肌营养不良。心脏受累主要表现为传导异常和心律失常。我们试图评估MD患者的舒张功能。对斯坦纳特病患者进行了超声心动图 - 多普勒检查,并通过组织多普勒成像(TDI)完成了一个对照组。本研究纳入了26例斯坦纳特病患者,并与一个对照组进行比较。两组的平均年龄相似(斯坦纳特病患者为45.1岁±10.9,对照组为42.1岁±11,P = 0.4)。26例斯坦纳特病患者中有6例左心室(LV)射血分数<50%。斯坦纳特病患者与对照组患者的平均左心房(LA)直径在统计学上存在差异(27.8 mm±8.5 vs 19.7 mm±4;P = 0.0018)。斯坦纳特病患者二尖瓣E/A峰比值平均为1.29±0.45,对照组为1.36±0.4(P = 0.6)。与对照组患者相比,我们发现斯坦纳特病患者二尖瓣E减速时间增加(219 ms±53 vs 176 ms±29;P = 0.013)。两组的平均侧壁舒张早期峰值速度Ea相似(12.3 cm/s±3 vs 13.1 cm/s±3.8;P = 0.50)。两组的平均室间隔舒张早期峰值速度相似(11.2 cm/s±2 vs 10.4±2;P = 0.51)。我们发现斯坦纳特病患者的LA直径增加以及二尖瓣减速时间增加,提示舒张功能异常。

相似文献

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本文引用的文献

6
Myotonic dystrophy and the heart.强直性肌营养不良症与心脏
Heart. 2002 Dec;88(6):665-70. doi: 10.1136/heart.88.6.665.
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Cardiac disease in myotonic dystrophy.强直性肌营养不良症中的心脏疾病
Cardiovasc Res. 1997 Jan;33(1):13-22. doi: 10.1016/s0008-6363(96)00163-0.

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