Topiramate dose effects on cognition: a randomized double-blind study

• Published in: Neurology Vol. 76; no. 2; p. 131
• Main Authors: Loring, D W, Williamson, D J, Meador, K J, Wiegand, F, Hulihan, J
• Format: Journal Article
• Language: English
• Published: United States 11.01.2011
• Subjects: Adult; Anticonvulsants - administration & dosage; Anticonvulsants - adverse effects; Body Mass Index; Body Weight - drug effects; Cognition - drug effects; Dose-Response Relationship, Drug; Double-Blind Method; Female; Fructose - administration & dosage; Fructose - adverse effects; Fructose - analogs & derivatives; Humans; Male; Middle Aged; Neuropsychological Tests; Time Factors; Treatment Outcome
• ISSN: 1526-632X
• DOI: 10.1212/WNL.0b013e318206ca02

Topiramate (TPM), a broad-spectrum antiepileptic drug, has been associated with neuropsychological impairment in patients with epilepsy and in healthy volunteers. To establish whether TPM-induced neuropsychological impairment emerges in a dose-dependent fashion and whether early cognitive response (6-week) predicts later performance (24-week). Computerized neuropsychological assessment was performed on 188 cognitively normal adults who completed a double-blind, placebo-controlled, parallel-group, 24-week, dose-ranging study which was designed primarily to assess TPM effects on weight. Target doses were 64, 96, 192, or 384 mg per day. The Computerized Neuropsychological Test Battery was administered at baseline and 6, 12, and 24 weeks. Individual cognitive change was established using reliable change index (RCI) analysis. Neuropsychological effects emerged in a dose-dependent fashion in group analyses (p < 0.0001). RCI analyses showed a dose-related effect that emerged only at the higher dosing, with 12% (64 mg), 8% (96 mg), 15% (192 mg), and 35% (384 mg) of subjects demonstrating neuropsychological decline relative to 5% declining in the placebo group. Neuropsychological change assessed at 6 weeks significantly predicted individual RCI outcome at 24 weeks. Neuropsychological impairment associated with TPM emerges in a dose-dependent fashion. Subjects more likely to demonstrate cognitive impairment after 24 weeks of treatment can be identified early on during treatment (i.e., within 6 weeks). RCI analysis provides a valuable approach to quantify individual neuropsychological risk.