Fagan E R, Taylor M J
Division of Neurology, Hospital for Sick Children, University of Toronto, Ontario, Canada.
Can J Neurol Sci. 1987 Nov;14(4):617-21.
Recent studies have reported that in abetalipoproteinaemia patients high dose vitamin E therapy may arrest or improve the neurological syndrome. Five patients with abetalipoproteinaemia have been followed since 1982, when all were started on high dose vitamin E therapy. Auditory brainstem responses (ABR), visual evoked potentials (VEP), and sensory evoked potentials (SEP) were recorded every six to twelve months. The vitamin E levels stayed below normal range in all patients; the neurological status remained relatively stable in most of the patients over the four years. The ABRs were consistently normal in all patients over the period of study. The VEPs improved in one patient with introduction of vitamin E therapy, and remained stable in the others, one of whom always had abnormal VEPs. The cortical SEPs were abnormal in all but the least affected patient and fluctuated in the two patients who also demonstrated some deterioration in neurological status. These results suggest that serial assessments combining neurological and neurophysiological studies provide important information in the follow-up of patients with abetalipoproteinaemia and that the SEP is the evoked potential best suited for the detection of the neurological changes in this disorder.
近期研究报告称,对于无β脂蛋白血症患者,高剂量维生素E疗法可能会阻止或改善神经综合征。自1982年起,对5例无β脂蛋白血症患者进行了随访,当时所有患者均开始接受高剂量维生素E治疗。每6至12个月记录一次听觉脑干反应(ABR)、视觉诱发电位(VEP)和感觉诱发电位(SEP)。所有患者的维生素E水平均低于正常范围;在四年期间,大多数患者的神经状态保持相对稳定。在研究期间,所有患者的ABR始终正常。一名患者在开始维生素E治疗后VEP有所改善,其他患者的VEP保持稳定,其中一名患者的VEP始终异常。除了受影响最小的患者外,所有患者的皮质SEP均异常,并且在神经状态也出现一些恶化的两名患者中,SEP有所波动。这些结果表明,结合神经学和神经生理学研究的系列评估为无β脂蛋白血症患者的随访提供了重要信息,并且SEP是最适合检测该疾病神经变化的诱发电位。