Lampl Christian, Bonelli Silvia, Ransmayr Gerhard
Pain and Headache Centre, Department of Neurology and Psychiatry, General Hospital Linz, Austria.
Headache. 2004 Feb;44(2):174-6. doi: 10.1111/j.1526-4610.2004.04036.x.
To evaluate the efficacy of topiramate in the treatment of migraine aura. Antiepileptic drugs may be useful in migraine prevention through such mechanisms as acting directly on the nociceptive system or by modulating the biochemical phenomena of aura. Topiramate acts directly on N-methyl-d-aspartate and amino-3-hydroxy-5-methylisoxazole-4-propionic acid/kainate glutamate receptors and modulates calcium ion channel activity by inhibiting high-voltage-activated L-type calcium ion channels.
Twelve patients with migraine with aura were enrolled in an open-label study and treated with topiramate for 6 months. The dose of topiramate was increased weekly by 25 mg up to a daily dose of 100 mg after 4 weeks.
In all 12 patients after 6 months of treatment, topiramate did not statistically influence aura frequency (P=.317) or duration (P=.480) compared with baseline. Mild to moderate side effects were observed, but they did not interfere with treatment. Consistent with previous observations, migraine frequency as well as headache intensity and duration improved statistically significantly.
Topiramate is not effective in preventing migraine aura.
评估托吡酯治疗偏头痛先兆的疗效。抗癫痫药物可能通过直接作用于伤害感受系统或调节先兆的生化现象等机制,对偏头痛预防有效。托吡酯直接作用于N-甲基-D-天冬氨酸和氨基-3-羟基-5-甲基异恶唑-4-丙酸/海人藻酸谷氨酸受体,并通过抑制高电压激活的L型钙离子通道来调节钙离子通道活性。
12例伴有先兆的偏头痛患者参与一项开放标签研究,接受托吡酯治疗6个月。托吡酯剂量每周增加25mg,4周后达到每日100mg的剂量。
治疗6个月后,所有12例患者中,与基线相比,托吡酯对先兆频率(P = 0.317)或持续时间(P = 0.480)无统计学影响。观察到轻度至中度副作用,但未干扰治疗。与先前观察结果一致,偏头痛频率以及头痛强度和持续时间有统计学显著改善。
托吡酯对预防偏头痛先兆无效。