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Autonomic Dysfunction in Wilsons Disease: A Comprehensive Evaluation during a 3-Year Follow Up

机译:威尔逊氏病中的自主神经功能障碍:三年随访期间的综合评估

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>Objectives: Wilson's disease is reported to have autonomic dysfunction, but comprehensive evaluation of autonomic function is lacking. Additionally, little is known about the change of autonomic function of Wilson's disease during continuous therapy. We assumed that patients with Wilson's disease had both sympathetic and parasympathetic autonomic impairments, and the autonomic dysfunction might be stable across a 3-year follow-up after years of optimal treatment.>Methods: Twenty-six patients with Wilson's disease and twenty-six healthy controls were recruited. Twenty patients in the Wilson's disease group were examined again after a 3-year follow-up. All the participants were evaluated by a questionnaire on dysautonomia symptoms, 24-h blood pressure and heart rate monitoring, and cardiovascular autonomic function examination in various conditions including at rest, deep breathing, Valsalva maneuver, isometric handgrip test and passive tilting. Baroreflex sensitivity and spectral analyses were performed via trigonometric regressive spectral analysis.>Results: Patients with Wilson's disease showed autonomic dysfunction mainly in the following aspects: (1) the heart rate was higher than the controls. (2) Valsalva ratio was lower in patients with Wilson's disease compared with the controls. (3) Heart rate increase during isometric hand gripping was smaller in the Wilson's disease patients than the controls. (4) Baroreflex sensitivity was lower during nearly all the cardiovascular autonomic function examinations compared with healthy controls. When tested 3 years later, baroreflex sensitivity at rest decreased compared with baseline. (5) There were mild declines of resting DBP and low frequency component of heart rate variability during the follow-up examination compared with baseline. (6) Subgroup analysis showed that patients initially presenting with neurological symptoms had a higher night-time heart rate, lower expiration: inspiration RR interval ratio (E/I ratio), lower expiration: inspiration RR interval difference (E-I difference), less increase of heart rate and diastolic blood pressure during the handgrip test, and lower baroreflex sensitivity during deep breathing than the control group. (7) Correlation analysis showed that the severity of neurological symptoms was associated with E/I ratio, E-I difference, Valsalva ratio, heart rate change during the handgrip test, and baroreflex sensitivity during deep breathing.>Conclusions: The present study reveals cardiovascular autonomic dysfunction involving both sympathetic and parasympathetic branches in Wilson's disease patients, which is especially significant in the patients with neurological onset. Autonomic function is generally stable undergoing optimal maintenance treatment in patients with Wilson's disease. Though there might be mild changes of specific parameters.
机译:>目的:据报道,威尔逊氏病具有自主神经功能障碍,但缺乏对自主神经功能的全面评估。另外,关于连续治疗期间威尔逊氏病的自主神经功能改变的知之甚少。我们假设威尔逊氏病患者同时患有交感神经系统和副交感神经系统的自主神经功能障碍,经过多年的最佳治疗,其自主神经功能障碍在三年的随访中可能保持稳定。>方法:招募了威尔逊氏病和26位健康对照。在进行了3年的随访后,再次检查了威尔逊病组的20名患者。通过问卷调查对所有参与者进行评估,包括:自主神经功能紊乱症状,24小时血压和心率监测以及各种条件下的心血管自主功能检查,包括休息,深呼吸,Valsalva动作,等距握力测试和被动倾斜。通过三角回归光谱分析进行压力反射敏感性和光谱分析。>结果:威尔逊氏病患者的自主神经功能障碍主要表现在以下几个方面:(1)心率高于对照组。 (2)与对照组相比,威尔逊氏病患者的缬草比率要低。 (3)在威尔逊氏病患者中,等距握持过程中的心率增加幅度小于对照组。 (4)与健康对照组相比,几乎所有心血管自主功能检查期间的压力反射敏感性均较低。 3年后进行测试时,与基线相比,静止时的压力反射敏感性降低。 (5)与基线相比,随访期间静息DBP轻度下降,心率变异性的低频成分略有下降。 (6)亚组分析显示,最初出现神经系统症状的患者夜间心率较高,呼气:吸气RR间隔比(E / I比)较低,呼气:吸气RR间隔差(EI差),增加较少握力测试期间心率和舒张压的变化,以及深呼吸时压力反射敏感性低于对照组。 (7)相关性分析表明,神经系统症状的严重程度与E / I比,EI差异,Valsalva比,手握测试期间的心率变化以及深呼吸时的压力反射敏感性有关。>结论:本研究揭示了在威尔逊病患者中涉及交感神经和副交感神经的心血管自主神经功能障碍,在神经系统疾病患者中尤为明显。经过威尔逊氏病患者的最佳维持治疗,其自主神经功能通常是稳定的。虽然特定参数可能会有轻微变化。

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