Memantine for the patients with mild cognitive impairment in Parkinson’s disease: a pharmacological fMRI study

Author:

Kawashima Shoji,Shimizu Yoko,Horiba Mitsuya,Ueki Yoshino,Akanabe Ryohei,Kan Hirohito,Kasai Haruaki,Kunitomo Hiroshi,Tanaka Satoshi,Toyota Takenari,Kawashima Shoji,Mizuno Masayuki,Okita Kenji,Matsukawa Noriyuki,Matsukawa Noriyuki,

Abstract

Abstract Background Mild cognitive impairment in Parkinson’s disease (PD-MCI) is associated with an increased risk of cognitive decline. PD-MCI is characterized by impairments in executive function and visuospatial recognition. The visuospatial n-back test is useful for assessing both domains. The 0-back test reflects visuospatial recognition, while the 1-back and 2-back tests reflect working memory. Cholinesterase inhibitors are effective in the treatment of PD-MCI and dementia in PD (PDD). Although some studies have reported the efficacy of memantine for PDD, the therapeutic efficacy of memantine in patients with PD-MCI remains uncertain. Methods This study aimed to investigate the effects of memantine on brain function in patients with PD-MCI, using a randomized double-blinded crossover protocol and functional MRI (fMRI). Ten patients who completed 16 weeks of follow-up were included. They were randomly assigned to either the memantine or placebo. Patients in the memantine group received 5 mg/day of memantine in the first week. The memantine dose was increased by 5 mg/day per week, until a final dose of 20 mg/day. Patients in the placebo group received the placebo following the same regimen as memantine. After the intervention, they underwent a 4 weeks washout period. Following the crossover protocol, a second intervention was conducted after the washout period. In each intervention, fMRI and neuropsychological tests were performed at the maximum dose period. Comparing the memantine and placebo groups, we investigated difference in the brain regions using the visuospatial n-back test. Results There were no significant regions enhanced by memantine comparing with placebo at any load of n-back tests. In contrast, exploring regions reduced by memantine, we found significant reduction of activations within right lingual gyrus and left superior frontal gyrus in comparison between 2-back and 0-back test. A number of correct answers of the 2-back test and time to complete Trail Making Test-A were worse during memantine intervention. Conclusions Memantine did not improve visuospatial working memory of the patients with PD-MCI. Treatment for PD should be planned carefully considering the impact on cognitive function. Further study is needed to establish new therapeutic strategy. Trial registration UMIN000046104. Retrospectively registered. First registration date: 28 Sept 2017.

Funder

Grants-in-Aid for Scientific Research on Priority Areas

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),General Medicine

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