Kiuru S, Matikainen E, Kupari M, Haltia M, Palo J
Department of Neurology, University of Helsinki, Finland.
J Neurol Sci. 1994 Oct;126(1):40-8. doi: 10.1016/0022-510x(94)90092-2.
Familial amyloidosis, Finnish type (FAF), is a gelsolin-related inherited systemic amyloidosis. We report autonomic nervous system and cardiac findings in a study of 30 FAF patients (18 females, 12 males aged 27-74 years; mean 53.9 years). Cardiovascular reflex tests showed a significant decrease in heart rate variation in FAF patients compared with healthy controls. Orthostatic hypotension was found in 9 of 28 FAF patients, but only in 3 of 69 controls. Signs of amyloid cardiopathy were rare at clinical examination and in radio-, echocardio- and electrocardiographic examinations. Histological and immunohistochemical studies revealed amyloid deposition and immunoreactivity against the gelsolin-related FAF amyloid subunit in autonomic nervous system structures and in cardiac tissue in 3 autopsied FAF patients. The results show that minor autonomic nervous system dysfunction can be found in FAF, while clinically significant amyloid cardiopathy or autonomic neuropathy is not characteristic of this type of amyloidosis.
芬兰型家族性淀粉样变性(FAF)是一种与凝溶胶蛋白相关的遗传性全身性淀粉样变性。我们报告了对30例FAF患者(18例女性,12例男性,年龄27 - 74岁;平均53.9岁)的自主神经系统和心脏检查结果。心血管反射测试显示,与健康对照相比,FAF患者的心率变异性显著降低。28例FAF患者中有9例出现直立性低血压,而69例对照中只有3例出现。在临床检查以及放射、超声心动图和心电图检查中,淀粉样心肌病的体征罕见。组织学和免疫组化研究显示,3例接受尸检的FAF患者的自主神经系统结构和心脏组织中存在淀粉样沉积以及针对与凝溶胶蛋白相关的FAF淀粉样亚单位的免疫反应性。结果表明,FAF患者可出现轻微的自主神经系统功能障碍,而临床上显著的淀粉样心肌病或自主神经病变并非这种类型淀粉样变性的特征。