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Amantadine As a Potential Treatment for Marchiafava-Bignami Disease: Case Reports and a Possible Mechanism

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Publisher Wiley
Specialty Neurology
Date 2022 Apr 21
PMID 35444836
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Abstract

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. . 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. . 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.

Citing Articles

Clinical analysis of Marchiafava-Bignami disease.

Liu C, Wang H, Xie B, Tian S, Ding Y BMC Neurol. 2024; 24(1):389.

PMID: 39402444 PMC: 11472522. DOI: 10.1186/s12883-024-03901-y.


Marchiafava-Bignami disease: Case presentation and radiological imaging.

Waack A, Nandwani S, Ranabothu M, Ranabothu A, Vattipally V Radiol Case Rep. 2023; 18(11):3922-3925.

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References
1.
Heinrich A, Runge U, Khaw A . Clinicoradiologic subtypes of Marchiafava-Bignami disease. J Neurol. 2004; 251(9):1050-9. DOI: 10.1007/s00415-004-0566-1. View

2.
Gass A, Birtsch G, Olster M, Schwartz A, Hennerici M . Marchiafava-Bignami disease: reversibility of neuroimaging abnormality. J Comput Assist Tomogr. 1998; 22(3):503-4. DOI: 10.1097/00004728-199805000-00026. View

3.
Logan C, Asadi H, Kok H, Looby S, Brennan P, OHare A . Neuroimaging of chronic alcohol misuse. J Med Imaging Radiat Oncol. 2016; 61(4):435-440. DOI: 10.1111/1754-9485.12572. View

4.
Kornhuber J, Weller M, Schoppmeyer K, Riederer P . Amantadine and memantine are NMDA receptor antagonists with neuroprotective properties. J Neural Transm Suppl. 1994; 43:91-104. View

5.
Staszewski J, Macek K, Stepien A . [Reversible demyelinisation of corpus callosum in the course of Marchiafava-Bignami disease]. Neurol Neurochir Pol. 2006; 40(2):156-61. View