Lugaresi Elio, Provini Federica
Department of Neurological Sciences, University of Bologna, Italy.
Rev Neurol Dis. 2007 Summer;4(3):145-52.
This review summarizes the pioneering steps culminating in the identification of a novel disease, fatal familial insomnia (FFI), a hereditary prion disease. Together with Morvan's chorea and delirium tremens, FFI is characterized by an inability to sleep associated with motor and autonomic overactivation. We named this pattern agrypnia excitata, a syndrome caused by a dysfunction in thalamolimbic circuits. This review highlights the strategic role of the limbic thalamus in the central autonomic network running from the limbic cortex to the lower brainstem and regulating sleep and wakefulness.
本综述总结了一系列开创性的研究步骤,最终确定了一种新型疾病——致死性家族性失眠症(FFI),这是一种遗传性朊病毒病。与莫旺氏舞蹈症和震颤谵妄一样,FFI的特征是无法入睡,并伴有运动和自主神经功能亢进。我们将这种模式命名为激越性失眠,这是一种由丘脑边缘回路功能障碍引起的综合征。本综述强调了边缘丘脑在从边缘皮质到脑干下部的中枢自主神经网络中的战略作用,该网络调节睡眠和觉醒。