Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria.
Department of Neuroradiology, Innsbruck Medical University, Innsbruck, Austria.
Clin Auton Res. 2018 Jun;28(3):341-346. doi: 10.1007/s10286-018-0504-4. Epub 2018 Feb 12.
To assess whether autonomic failure belongs to the clinical spectrum of spinocerebellar ataxia type 2 (SCA2), an autosomal dominant genetic disorder showing progressive cerebellar and brainstem dysfunction.
We evaluated cardiovascular autonomic function in 8 patients with SCA2 and 16 age- and gender-matched healthy controls. Other autonomic domains were examined through standardized questionnaires and by testing the skin sympathetic reflex.
Patients with SCA2 showed normal responses to cardiovascular autonomic function tests, with the exception of lower baroreflex sensitivity upon standing compared to controls. In questionnaires, 7 out of 8 patients reported bladder disturbances, while 3 out of 6 tested patients had no skin sympathetic reflex.
We did not observe clinically overt cardiovascular autonomic failure in patients with SCA2. Other autonomic domains (i.e., bladder and sudomotor function) may be affected in the disease.
评估自主神经衰竭是否属于脊髓小脑共济失调 2 型(SCA2)的临床谱系,SCA2 是一种常染色体显性遗传疾病,表现为进行性小脑和脑干功能障碍。
我们评估了 8 例 SCA2 患者和 16 名年龄和性别匹配的健康对照者的心血管自主神经功能。通过标准化问卷和皮肤交感反射测试来检查其他自主神经域。
SCA2 患者的心血管自主神经功能测试结果正常,除了与对照组相比站立时下的血压反射敏感性较低。在问卷调查中,8 例患者中有 7 例报告了膀胱功能障碍,而在 6 例接受测试的患者中,有 3 例没有皮肤交感反射。
我们没有观察到 SCA2 患者出现明显的心血管自主神经衰竭。疾病可能会影响其他自主神经域(即膀胱和汗腺功能)。