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托吡酯相关工作记忆损伤严重程度受血药浓度和工作记忆能力调节。

Severity of Topiramate-Related Working Memory Impairment Is Modulated by Plasma Concentration and Working Memory Capacity.

机构信息

Experimental and Clinical Pharmacology Department, University of Minnesota, Minneapolis, Minnesota, USA.

出版信息

J Clin Pharmacol. 2020 Sep;60(9):1166-1176. doi: 10.1002/jcph.1611. Epub 2020 Apr 16.

Abstract

Drug side effects that impair cognition can lead to diminished quality of life and discontinuation of therapy. Topiramate is an antiepileptic drug that elicits cognitive deficits more frequently than other antiepileptic drugs, impairing multiple cognitive domains including language, attention, and memory. Although up to 40% of individuals taking topiramate may experience cognitive deficits, we are currently unable to predict which individuals will be most severely affected before administration. The objective of this study was to show the contributions of plasma concentration and working memory capacity in determining the severity of an individual's topiramate-related cognitive impairment. Subjects were enrolled in a double-blind, placebo-controlled crossover study during which they received a single dose of either 100, 150, or 200 mg topiramate. Working memory function was assessed using a modified Sternberg working memory task with 3 memory loads administered 4 hours after dosing. After adjustment for differences in working memory capacity, each 1 μg/mL of topiramate plasma concentration was associated with a 3.6% decrease in accuracy for all memory loads. Placebo effects occurred as a function of working memory capacity, with individuals with high working memory capacity experiencing less severe placebo-related impairment compared with those with low working memory capacity. Our results demonstrate that severity of topiramate-related cognitive deficits occurs as a function of both drug exposure and baseline cognitive function. By identifying patient- and exposure-related characteristics that modulate the severity of cognitive side effects, topiramate dosing strategies may be individually tailored in the future to prevent unwanted cognitive impairment.

摘要

药物的副作用会损害认知能力,导致生活质量下降,并停止治疗。托吡酯是一种抗癫痫药物,比其他抗癫痫药物更频繁地引起认知障碍,损害包括语言、注意力和记忆在内的多个认知领域。尽管高达 40%的服用托吡酯的人可能会出现认知障碍,但我们目前无法预测哪些人在给药前会受到最严重的影响。本研究的目的是展示血浆浓度和工作记忆能力在确定个体托吡酯相关认知障碍严重程度方面的贡献。受试者参加了一项双盲、安慰剂对照交叉研究,在此期间,他们接受了单剂量的 100、150 或 200mg 托吡酯。工作记忆功能使用改良的 Sternberg 工作记忆任务进行评估,在给药后 4 小时进行 3 种记忆负荷。在调整工作记忆能力差异后,托吡酯血浆浓度每增加 1μg/ml,所有记忆负荷的准确性就会下降 3.6%。安慰剂效应是工作记忆能力的函数,具有高工作记忆能力的个体与具有低工作记忆能力的个体相比,安慰剂相关的损伤程度较轻。我们的研究结果表明,托吡酯相关认知障碍的严重程度是药物暴露和基线认知功能的共同作用。通过识别调节认知副作用严重程度的患者和暴露相关特征,未来可能会针对个体量身定制托吡酯的剂量策略,以预防不必要的认知障碍。

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