金刚烷胺作为一种潜在的治疗Marchiafava-Bignami病的方法:病例报告和可能的机制

IF 0.9 Q4 CLINICAL NEUROLOGY
Leenil C Noel, Martin A. Myers, Tigran Kesayan
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引用次数: 1

摘要

一些报告描述了金刚烷胺用于治疗marchiafawa - bignami病(MBD)的症状;然而,金刚烷胺在治疗MBD症状中的作用尚不清楚。在这里,我们描述了2例MBD患者,他们接受金刚烷胺治疗,并假设了一个潜在的机制,负责临床获益。案例1。一名38岁女性,饮酒过量,表现为躁动、语言障碍和最低限度的意识状态。MRI显示脾和膝病变。在诊断为MBD后,她接受了静脉注射硫胺素、多种维生素和100毫克金刚烷胺的治疗,每天两次,持续2周。3周后恢复至接近基线水平。例2。54岁女性,多年重度饮酒,表现为突发性腹泻、失算、行为失调、虚弱和尿失禁。MRI显示胼胝体前部大病变。在MBD最初康复两年后,她注意到,饮用“能量饮料”导致她残留的行为、疲劳和语言症状短暂、几乎完全消失。100毫克的金刚烷胺,每天两次的试验。在明显改善后,进一步增加至200毫克,每天3次,可显著改善语言和行为症状。结论金刚烷胺加维生素治疗MBD可能有益。金刚烷胺的多巴胺能作用可能导致多巴胺介导通路的恢复和功能改善,包括初始恢复期间的中皮层和中边缘通路,以及随后几个月的语言、行为和疲劳改善。金刚烷胺在MBD治疗中的作用有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Amantadine as a Potential Treatment for Marchiafava–Bignami Disease: Case Reports and a Possible Mechanism
Introduction Several reports have described the use of amantadine for managing symptoms in Marchiafava–Bignami disease (MBD); however, amantadine's role for the treatment of MBD symptoms is unclear. Here, we describe 2 patients with MBD who were treated with amantadine and hypothesize a potential mechanism responsible for clinical benefit. Case 1. A 38-year-old woman with excessive wine drinking presented with agitation, impaired speech, and a minimally conscious state. MRI revealed lesions in the splenium and genu. After being diagnosed with MBD, she was treated with intravenous thiamine, multivitamins, and 100 mg of amantadine twice a day for 2 weeks. She recovered to near baseline after 3 weeks. Case 2. A 54-year-old woman with years of heavy alcohol use presented with sudden bradyphrenia, acalculia, disinhibited behavior, weakness, and urinary incontinence. MRI revealed a large anterior callosal lesion. Two years after initial recovery from MBD, she noted that consuming “energy drinks” resulted in a transient, near-complete resolution of her residual behavioral, fatigue, and language symptoms. 100 mg of amantadine twice a day was trialled. After noted improvement, a further escalation to 200 mgs 3 times a day resulted in significant improvement in language and behavioral symptoms. Conclusion Amantadine in addition to vitamins may be beneficial in the treatment of MBD. It is possible that the dopaminergic effect of amantadine leads to improved recovery and function in dopamine-mediated pathways, including mesocortical and mesolimbic pathways during initial recovery, as well as improved speech, behavior, and fatigue in the following months. The role of amantadine in the treatment of MBD warrants further study.
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