Meier Andreas, Mollenhauer Brit, Cohrs Stefan, Rodenbeck Andrea, Jordan Wolfgang, Meller Johannes, Otto Markus
Department of Psychiatry and Psychotherapy, Sleep Disorders Center, Georg-August-University, von-Siebold-Strasse 5, 37075 Goettingen, Germany.
Brain Res. 2005 Nov 30;1063(2):201-3. doi: 10.1016/j.brainres.2005.09.028. Epub 2005 Nov 2.
A significant atrophy and loss of hypocretin neurons in the brains of human patients with Huntington's disease (HD) and in R6/2 mice have been reported. We included 10 patients with HD and 12 patients with chorea-like hyperkinetic movement disorders (non-HD). All patients of the HD group and eleven patients of the non-HD group showed normal hypocretin-1 levels. Thus, hypocretin-1 may not serve as an additional diagnostic marker for HD.
据报道,患有亨廷顿舞蹈症(HD)的人类患者大脑及R6/2小鼠体内的下丘脑分泌素神经元出现了显著萎缩和缺失。我们纳入了10名HD患者和12名患有舞蹈症样运动障碍(非HD)的患者。HD组的所有患者以及非HD组的11名患者下丘脑分泌素-1水平均正常。因此,下丘脑分泌素-1可能无法作为HD的额外诊断标志物。