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Effect of Rivastigmine or Memantine Add-on Therapy Is Affected by Butyrylcholinesterase Genotype in Patients with Probable Alzheimer's Disease

Authors
Han, Hyun JeongKwon, Jay C.Kim, Jung EunKim, Shin GyeomPark, Jong-MooPark, Kyung WonPark, Key ChungPark, Kee HyungMoon, So YoungSeo, Sang WonChoi, Seong HyeCho, Soo-Jin
Issue Date
2015
Publisher
S. Karger AG
Keywords
Alzheimer's disease; Butyrylcholinesterase; Cognition; Apolipoprotein E epsilon 4
Citation
European Neurology, v.73, no.1-2, pp 23 - 28
Pages
6
Journal Title
European Neurology
Volume
73
Number
1-2
Start Page
23
End Page
28
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/11548
DOI
10.1159/000366198
ISSN
0014-3022
1421-9913
Abstract
Background: The K variant of butyrylcholinesterase (BCHE-K) exhibits a reduced acetylcholine-hydrolyzing capacity; so the clinical response to rivastigmine may differ in Alzheimer's disease (AD) patients with the BCHE-K gene. Objective: To investigate the clinical response to rivastigmine transdermal patch monotherapy or mennantine plus rivastigmine transdermal patch therapy in AD patients based on the BCHE-K gene. Methods: A total of 146 probable AD patients consented to genetic testing for butyrylcholinesterase and underwent the final efficacy evaluations. Responders were defined as patients with an equal or better score on the Alzheimer's Disease Assessment Scale-cognitive subscale (ADAS-cog) at 16 weeks compared to their baseline score. Results: BCHE-K carriers showed a lower responder rate on the ADAS-cog than non-carriers (38.2 vs. 61.7%, p = 0.02), and this trend was evident in AD patients with apolipoprotein E epsilon 4 (35 vs. 60.7%, p = 0.001). The presence of the BCHE-K allele predicted a worse response on the ADAS-cog (odds ratio 0.35, 95% confidence interval 0.14-0.87), after adjusting for demographic and baseline cognitive and functional variables. Conclusion: The BCHE-K genotype may be related to a poor cognitive response to rivastigmine patch or me-mantine add-on therapy, especially in the presence of apoli-poprotei n E epsilon 4. (C) 2014 S. Karger AG, Basel
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