Cardiac function evaluation in children with spinal muscular atrophy: A case-control study.

IF 1 4区 医学 Q3 PEDIATRICS
Xiufang He, Xuandi Li, Mengzhen Yan, Huimin Peng, Lili Zhang, Yujian Liang, Wen Tang, Shujuan Li
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引用次数: 0

Abstract

Background: Spinal muscular atrophy (SMA) is an autosomal recessive disorder characterized by degeneration of lower motor neurons, resulting in progressive muscle weakness and atrophy. However, little is known regarding the cardiac function of children with SMA.

Methods: We recruited SMA patients younger than 18 years of age from January 1, 2022, to April 1, 2022, in the First Affiliated Hospital of Sun Yat-sen University. All patients underwent a comprehensive cardiac evaluation before treatment, including history taking, physical examination, blood tests of cardiac biomarkers, assessment of echocardiography and electrocardiogram. Age/gender-matched healthy volunteers were recruited as controls.

Results: A total of 36 SMA patients (26 with SMA type 2 and 10 with SMA type 3) and 40 controls were enrolled in the study. No patient was clinically diagnosed with heart failure. Blood tests showed elevated values of creatine kinase isoenzyme M and isoenzyme B (CK-MB) mass and high-sensitivity cardiac troponin T (hs-cTnT) in spinal muscular atrophy (SMA) patients. Regarding echocardiographic parameters, SMA children were detected with lower global left and right ventricular longitudinal strain, abnormal diastolic filling velocities of trans-mitral and trans-tricuspid flow. The results revealed no clinical heart dysfunction in SMA patients, but subclinical ventricular dysfunction was seen in SMA children including the diastolic function and myocardial performance. Some patients presented with elevated heart rate and abnormal echogenicity of aortic valve or wall. Among these SMA patients, seven patients (19.4%) had scoliosis. The Cobb's angles showed a significant negative correlation with LVEDd/BSA, but no correlation with other parameters, suggesting that mild scoliosis did not lead to significant cardiac dysfunction.

Conclusions: Our findings warrant increased attention to the cardiac status and highlight the need to investigate cardiac interventions in SMA children.

脊髓性肌肉萎缩症患儿的心功能评估:病例对照研究
背景:脊髓性肌萎缩症(SMA)是一种常染色体隐性遗传疾病,其特征是下运动神经元变性,导致进行性肌肉无力和萎缩。然而,人们对 SMA 儿童的心脏功能知之甚少:我们从 2022 年 1 月 1 日至 2022 年 4 月 1 日在中山大学附属第一医院招募了年龄小于 18 岁的 SMA 患者。所有患者在治疗前均接受了全面的心脏评估,包括病史采集、体格检查、心脏生物标志物血液检测、超声心动图和心电图评估。对照组为年龄/性别匹配的健康志愿者:共有 36 名 SMA 患者(26 名 SMA 2 型患者和 10 名 SMA 3 型患者)和 40 名对照组参加了研究。没有患者被临床诊断为心力衰竭。血液化验结果显示,脊髓性肌萎缩症(SMA)患者肌酸激酶同工酶 M 和同工酶 B(CK-MB)质量和高敏心肌肌钙蛋白 T(hs-cTnT)值升高。在超声心动图参数方面,SMA 患儿的左心室和右心室整体纵向应变较低,经瓣膜和经三尖瓣血流的舒张期充盈速度异常。结果显示,SMA 患者没有临床心脏功能障碍,但在 SMA 儿童中发现了亚临床心室功能障碍,包括舒张功能和心肌表现。部分患者出现心率增快、主动脉瓣或主动脉壁回声异常。在这些 SMA 患者中,7 名患者(19.4%)有脊柱侧弯。Cobb角与LVEDd/BSA呈显著负相关,但与其他参数无相关性,这表明轻度脊柱侧弯不会导致明显的心功能不全:我们的研究结果表明,应更加关注SMA患儿的心脏状况,并强调研究心脏干预措施的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pediatrics International
Pediatrics International 医学-小儿科
CiteScore
2.00
自引率
7.10%
发文量
519
审稿时长
12 months
期刊介绍: Publishing articles of scientific excellence in pediatrics and child health delivery, Pediatrics International aims to encourage those involved in the research, practice and delivery of child health to share their experiences, ideas and achievements. Formerly Acta Paediatrica Japonica, the change in name in 1999 to Pediatrics International, reflects the Journal''s international status both in readership and contributions (approximately 45% of articles published are from non-Japanese authors). The Editors continue their strong commitment to the sharing of scientific information for the benefit of children everywhere. Pediatrics International opens the door to all authors throughout the world. Manuscripts are judged by two experts solely upon the basis of their contribution of original data, original ideas and their presentation.
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