Merico Antonio, Cavinato Marianna
Department of Neurophysiology, San Camillo Foundation, Institute of Care and Research , Venice , Italy.
Amyotroph Lateral Scler. 2011 Sep;12(5):363-7. doi: 10.3109/17482968.2011.584628. Epub 2011 May 30.
Our objective was to assess the autonomic function of ALS patients with and without bulbar signs to characterize dysautonomia in ALS disease. Standard autonomic tests and spectral analysis of heart rate variability (HRV), reflecting changes in the sympathovagal balance, were examined in 33 ALS patients (14 with bulbar signs) and 30 controls. Results showed that in the supine position, ALS patients had significantly lower total power and absolute values of high-frequency power indicating a depressed sinus arrhythmia. Patients with bulbar signs showed more marked autonomic alterations at rest. Tilting did not induce the expected increase in low-frequency and decrease in high-frequency power of HRV in all patients. No correlation was found between autonomic tests and clinical parameters. Our findings suggest an early subclinical involvement of the autonomic system in ALS, particularly affecting parasympathetic cardiac control. Patients with prominent bulbar signs show a more severe autonomic dysfunction under resting conditions.
我们的目标是评估有和没有延髓体征的肌萎缩侧索硬化症(ALS)患者的自主神经功能,以明确ALS疾病中的自主神经功能障碍特征。对33例ALS患者(14例有延髓体征)和30名对照者进行了标准自主神经测试以及反映交感迷走神经平衡变化的心率变异性(HRV)频谱分析。结果显示,在仰卧位时,ALS患者的总功率和高频功率绝对值显著降低,表明窦性心律不齐受到抑制。有延髓体征的患者在静息时表现出更明显的自主神经改变。倾斜试验并未在所有患者中引起HRV低频功率的预期增加和高频功率的预期降低。自主神经测试与临床参数之间未发现相关性。我们的研究结果表明,自主神经系统在ALS中存在早期亚临床受累,尤其影响副交感神经对心脏的控制。有明显延髓体征的患者在静息状态下表现出更严重的自主神经功能障碍。