Cortical excitability during prolonged antiepileptic drug treatment and drug withdrawal

被引:39
作者
Lee, HW
Seo, HJ
Cohen, LG
Bagic, A
Theodore, WH
机构
[1] NINCDS, Human Cortical Physiol Sect, Med Neurol Branch, Bethesda, MD 20892 USA
[2] NINDS, Clin Epilepsy Sect, Bethesda, MD 20892 USA
[3] Ewha Womans Univ, Coll Med, Dept Neurol, Seoul 120750, South Korea
[4] Ewha Med Res Inst, Seoul, South Korea
关键词
conical excitability; transcranial magnetic stimulation; plasma blood levels; antiepileptic drug treatment; drug withdrawal;
D O I
10.1016/j.clinph.2004.12.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Previous reports characterized the effects of administration of single oral doses of antiepileptic drugs (AED) on cortical excitability. However, AED effects on cortical excitability, and their relationship to plasma blood levels, during chronic drug administration at therapeutic doses are not known. The objective of the study was to determine whether plasma blood levels during chronic administration at therapeutic doses would accurately predict changes in corticomotor excitability. Methods: We used transcranial magnetic stimulation (TMS) to measure cortical excitability during 5 weeks administration of carbamazepine (CBZ) and lamotrigine (LTG), and subsequent AED withdrawal in 20 healthy volunteers. Data were analyzed using ANOVA(RM) and regression analysis. Results: Resting motor thresholds (r-MT) increased with increasing total and free CBZ and LTG levels during drug administration, but not drug withdrawal. After acute AED withdrawal, r-MT elevation persisted in most individuals with CBZ despite undetectable plasma levels, compared to a rapid normalization with LTG. In contrast, acute drug withdrawal resulted in a transient decrease in r-MT in 3/10 individuals with CBZ and 2/10 with LTG. Conclusions: Plasma levels provide information on motor cortical function during active treatment phases but not during AED withdrawal. Significance: The transient decrease in r-MT associated with acute AED withdrawal could represent a physiological substrate contributing to AED withdrawal seizures. Published by Elsevier Ireland Ltd on behalf of International Federation of Clinical Neurophysiology.
引用
收藏
页码:1105 / 1112
页数:8
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