Brandes Jan L, Visser W Hester, Farmer Mildred V, Schuhl Amy L, Malbecq William, Vrijens France, Lines Christopher R, Reines Scott A
Nashville Neuroscience Group, Nashville, TN, USA.
Headache. 2004 Jun;44(6):581-6. doi: 10.1111/j.1526-4610.2004.446006.x.
To evaluate the efficacy and tolerability of montelukast 20 mg in the prophylactic treatment of migraine.
A previous small open-label study in migraine patients suggested prophylactic efficacy for montelukast, an antagonist of the cysteinyl leukotriene receptor that is used in the treatment of asthma. We sought to confirm these findings in a randomized controlled trial.
This multicenter, randomized, double-blind, placebo-controlled, parallel-groups study enrolled adult migraine outpatients who experienced > or =3 and < or =8 migraine attacks per month for the last 6 months. Patients were entered into a 2-month, single-blind, placebo run-in phase. Only patients who experienced > or =3 migraine attacks in the second month were eligible to enter the subsequent 3-month, double-blind treatment phase of the study. The primary efficacy endpoint was the percentage of patients reporting at least a 50% decrease in migraine attack frequency per month during the double-blind treatment period (months 3-5) compared to baseline (run-in month 2).
A total of 93 patients were randomized to montelukast 20 mg and 84 patients to placebo at the end of the placebo run-in month 2; 76 patients on montelukast and 72 patients on placebo completed the double-blind treatment period. Over 3 months of treatment, there was no significant difference between the two groups in the percentage of patients who reported at least a 50% decrease in migraine attack frequency per month: 15.4% for montelukast versus 10.3% for placebo (P= .304). In addition, montelukast 20 mg was not significantly superior to placebo on any of the secondary endpoints. There were no differences between treatment groups for adverse events.
Montelukast 20 mg was well tolerated in migraine patients but was not an effective prophylactic for prevention of migraine.
评估20毫克孟鲁司特预防性治疗偏头痛的疗效和耐受性。
先前一项针对偏头痛患者的小型开放标签研究表明,孟鲁司特(一种用于治疗哮喘的半胱氨酰白三烯受体拮抗剂)具有预防疗效。我们试图在一项随机对照试验中证实这些发现。
这项多中心、随机、双盲、安慰剂对照、平行组研究纳入了过去6个月每月经历≥3次且≤8次偏头痛发作的成年偏头痛门诊患者。患者进入为期2个月的单盲安慰剂导入期。只有在第二个月经历≥3次偏头痛发作的患者才有资格进入后续为期3个月的双盲治疗阶段。主要疗效终点是与基线(导入期第2个月)相比,在双盲治疗期(第3 - 5个月)报告每月偏头痛发作频率至少降低50%的患者百分比。
在安慰剂导入期第2个月末,共有93例患者被随机分配至20毫克孟鲁司特组,84例患者被分配至安慰剂组;76例服用孟鲁司特和72例服用安慰剂的患者完成了双盲治疗期。在3个月的治疗期间,两组中报告每月偏头痛发作频率至少降低50%的患者百分比无显著差异:孟鲁司特组为15.4%,安慰剂组为10.3%(P = 0.304)。此外,20毫克孟鲁司特在任何次要终点上均未显著优于安慰剂。治疗组之间不良事件无差异。
20毫克孟鲁司特在偏头痛患者中耐受性良好,但并非预防偏头痛的有效药物。