A multicenter, randomized clinical study to evaluate the effect on cognitive function of topiramate compared with valproate as add-on therapy to carbamazepine in patients with partial-onset seizures

被引:159
作者
Aldenkamp, AP
Baker, G
Mulder, OG
Chadwick, D
Cooper, P
Doelman, J
Duncan, R
Gassmann-Mayer, C
de Haan, GJ
Hughson, C
Hulsman, J
Overweg, J
Pledger, G
Rentmeester, TW
Riaz, H
Wroe, S
机构
[1] Epilepsy Ctr Kempenhaeghe, Dept Neurol, NL-5590 AB Heeze, Netherlands
[2] Epilepsy Ctr Kempenhaeghe, Dept Neuropsychol, NL-5590 AB Heeze, Netherlands
[3] Walton Hosp, Dept Neurosci, Liverpool L9 1AE, Merseyside, England
[4] Stichting Epilepsie Instellingen Nederland, Dept Neurol, Heemstede, Netherlands
[5] Hope Hosp, Dept Behav Med, Salford M6 8HD, Lancs, England
[6] So Gen Hosp, Inst Neurol Sci, Dept Neurol, Glasgow G51 4TF, Lanark, Scotland
[7] RW Johnson Pharmaceut Res Inst, Raritan, NJ 08869 USA
[8] RW Johnson Pharmaceut Res Inst, Bassersdorf, Switzerland
关键词
adverse effects; topiramate; cognitive function;
D O I
10.1111/j.1528-1157.2000.tb00322.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: This study compares the cognitive effects of topiramate (TPM) with those of valproate (VPA) using efficacious doses of each drug when used as adjunctive therapy to carbamazepine (CBZ). A key question of the study is to what extent a more gradual introduction of TPM improves tolerability and prevents cognitive impairment. Methods: The study is a multicenter, randomized, observer-blinded, parallel-group clinical trial with VPA or TPM given as first-line add-on therapy to steady-state treatment with CBZ. TPM is introduced at 25 mg and increased with weekly 25-mg/d increments to a minimum dosage of 200 mg/d. The target dosage ranges from 200 to 400 mg/d for TPM and is 1800 mg/d for VPA. The study evaluates cognitive function changes from baseline to end point (after 20 weeks of treatment) and during titration (after 8 weeks of treatment). The primary outcome measure is the difference between the treatments (TPM versus VPA) in change from baseline to end point and change from baseline to titration, using a 95% confidence interval approach. Results: For the 10 baseline-to-end point comparisons, one test measuring short-term verbal memory (Rey Auditory Verbal Learning Test) yields a statistically significant difference between the treatments (p = 0.02), showing worsening for TPM and improvement of scores for VPA. The 10 baseline-to-titration comparisons also show one statistically significant difference, again for a test measuring short-term memory (Recognition of Words; p = 0.04), showing a larger change in the negative direction for TPM. None of the mood tests or the test for subjective complaints shows statistically significant differences between the treatments, although more scores are in the negative direction for TPM during titration. Conclusion: Although the pattern of changes in the negative direction seems consistent with clinical information, the differences found between the treatments are small. An important finding of our study is that, when the results are compared with those of other studies, it is clear that gradual introduction of TPM can reduce the extent of cognitive impairment (with a maximum of about 0.6 SD).
引用
收藏
页码:1167 / 1178
页数:12
相关论文
共 28 条
[1]
Cognitive effects of lamotrigine as first-line add-on in patients with localization-related (partial) epilepsy [J].
Aldenkamp, AP ;
Mulder, OG ;
Overweg, J .
JOURNAL OF EPILEPSY, 1997, 10 (03) :117-121
[2]
The Neurotoxicity Scale .2. Results of a patient-based scale assessing neurotoxicity in patients with epilepsy [J].
Aldenkamp, AP ;
Baker, GA .
EPILEPSY RESEARCH, 1997, 27 (03) :165-173
[3]
THE NEUROTOXICITY SCALE - THE VALIDITY OF A PATIENT-BASED SCALE, ASSESSING NEUROTOXICITY [J].
ALDENKAMP, AP ;
BAKER, G ;
PIETERS, MSM ;
SCHOEMAKER, HC ;
COHEN, AF ;
SCHWABE, S .
EPILEPSY RESEARCH, 1995, 20 (03) :229-239
[4]
WITHDRAWAL OF ANTIEPILEPTIC MEDICATION IN CHILDREN EFFECTS ON COGNITIVE FUNCTION - THE MULTICENTER HOLMFRID STUDY [J].
ALDENKAMP, AP ;
ALPHERTS, WCJ ;
BLENNOW, G ;
ELMQVIST, D ;
HEIJBEL, J ;
NILSSON, HL ;
SANDSTEDT, P ;
TONNBY, B ;
WAHLANDER, L ;
WOSSE, E .
NEUROLOGY, 1993, 43 (01) :41-50
[5]
ALDENKAMP AP, 1996, EPILEPSIA, V37, P82
[6]
ALDENKAMP AP, 1992, ASSESSMENT COGNITIVE, P51
[7]
COMPUTERIZED NEUROPSYCHOLOGICAL ASSESSMENT OF COGNITIVE-FUNCTIONING IN CHILDREN WITH EPILEPSY [J].
ALPHERTS, WCJ ;
ALDENKAMP, AP .
EPILEPSIA, 1990, 31 :S35-S40
[8]
Double-blind, placebo-controlled trial of topiramate as add-on therapy in patients with refractory partial seizures [J].
BenMenachem, E ;
Henriksen, O ;
Dam, M ;
Mikkelsen, M ;
Schmidt, D ;
Reid, S ;
Reife, R ;
Kramer, L ;
Pledger, G ;
Karim, R .
EPILEPSIA, 1996, 37 (06) :539-543
[9]
Cohen J., 1998, Statistical Power Analysis for the Behavioral Sciences, V2nd
[10]
MEMORY AND PSYCHOMOTOR EFFECTS OF OXCARBAZEPINE IN HEALTHY-HUMAN VOLUNTEERS [J].
CURRAN, HV ;
JAVA, R .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1993, 44 (06) :529-533