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Mulibrey纳米症患儿的心脏功能障碍

Cardiac dysfunction in children with mulibrey nanism.

作者信息

Eerola A, Pihkala J I, Karlberg N, Lipsanen-Nyman M, Jokinen E

机构信息

Department of Pediatrics, University Hospital of Kuopio, Kuopio, Finland.

出版信息

Pediatr Cardiol. 2007 May-Jun;28(3):155-62. doi: 10.1007/s00246-006-0007-2. Epub 2007 Mar 20.

Abstract

Mulibrey nanism is an autosomal recessive disease with severe growth failure and multiple organ involvement. Heart manifestations include constrictive pericarditis and restrictive cardiomyopathy. The purpose of this study was to evaluate left ventricular (LV) diastolic and systolic function in children with mulibrey nanism utilizing two- and three- dimensional (2-D and 3-D) echocardiography and measurement of serum levels of natriuretic peptides. Of the 30 children diagnosed with mulibrey nanism in Finland, 26 participated. The control group comprised 26 children. In 2-D echocardiography, the interventricular septum and LV posterior wall were thicker in patients. The left atrium/aorta ratio measured a median 1.8 (range, 1.4-2.5) in patients and 1.3 (range, 1.0-1.7) in controls (p < 0.001). Patients differed from controls in several indices of diastolic LV function. In 3-D echocardiography, LV end diastolic volume measured a median of 51.9 ml/m(2) (range, 33.3-73.4) in patients and 59.7 ml/m(2) (range, 37.6-87.6) in controls (p = 0.040), and serum levels of N-terminal proatriopeptide and N-terminal pro-brain natriuretic peptide measured, respectively, a median of 0.54 nmol/L (range, 0.04-4.7) and 289 ng/L (range, 18-9170) in patients and 0.28 nmol/L (range, 0.09-0.72; p < 0.001) and 54 ng/L (range, 26-139; p < 0.001) in controls. They correlated with several indices of diastolic LV function. In a significant proportion of children with mulibrey nanism, myocardial function is impaired. Significant correlations appeared between indices of LV function, size of the left atrium, and levels of natriuretic peptides, showing that measurement of serum levels of natriuretic peptides is a useful follow-up method despite its dependence on loading conditions.

摘要

穆利布雷侏儒症是一种常染色体隐性疾病,伴有严重生长发育迟缓及多器官受累。心脏表现包括缩窄性心包炎和限制型心肌病。本研究旨在利用二维和三维超声心动图以及测量利钠肽血清水平来评估穆利布雷侏儒症患儿的左心室舒张和收缩功能。在芬兰确诊的30例穆利布雷侏儒症患儿中,26例参与了研究。对照组包括26名儿童。在二维超声心动图检查中,患者的室间隔和左心室后壁更厚。患者的左心房/主动脉比值中位数为1.8(范围1.4 - 2.5),对照组为1.3(范围1.0 - 1.7)(p < 0.001)。患者与对照组在左心室舒张功能的几个指标上存在差异。在三维超声心动图检查中,患者的左心室舒张末期容积中位数为51.9 ml/m²(范围33.3 - 73.4),对照组为59.7 ml/m²(范围37.6 - 87.6)(p = 0.040),患者的N末端前心钠素和N末端脑钠肽血清水平中位数分别为0.54 nmol/L(范围0.04 - 4.7)和289 ng/L(范围18 - 9170),对照组分别为0.28 nmol/L(范围0.09 - 0.72;p < 0.001)和54 ng/L(范围26 - 139;p < 0.001)。它们与左心室舒张功能的几个指标相关。在相当一部分穆利布雷侏儒症患儿中,心肌功能受损。左心室功能指标、左心房大小和利钠肽水平之间存在显著相关性,表明尽管血清利钠肽水平测量依赖于负荷状态,但它仍是一种有用的随访方法。

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