Pradalier A, Bakouche P, Baudesson G, Delage A, Cornaille-Lafage G, Launay J M, Biason P
Service de Médecine Interne IV, Consultation Migraine et Céphalées, Hôpital Louis Mourier, Colombes, France.
Cephalalgia. 2001 Oct;21(8):818-22. doi: 10.1046/j.1468-2982.2001.218240.x.
Omega-3 polyunsaturated fatty acids (OPFA) have beneficial effects on inflammatory reactions and production of cytokines. They decrease the release of 5HT by platelets and possess vasorelaxant activity. This led them to be tried in the prophylactic treatment of migraine. After 4 weeks of a single-blind placebo run-in period, patients were randomized and treated in double-blind condition by placebo or OPFA 6 g a day for 16 weeks, followed by a 4-week placebo run-out period. The intention to treat population included 196 patients. Those who received all four treatment periods included 96 patients taking OPFA and 87 taking placebo. The primary efficacy analysis was the number of migraine attacks during the last 4 weeks of treatment. During this period, the mean number of attacks was 1.20 +/- 1.40 in the OPFA group and 1.26 +/- 1.11 in the placebo group (NS). The total number of attacks during the 4-month period of the study was significantly different between groups: 7.05 in the placebo group, 5.95 in the OPFA group (P = 0.036). Mean intensity, mean duration of the attacks and rescue medication use, were not significantly different between the two groups. Except for a significant difference against OPFA for eructations, the tolerance was satisfying. Despite a run-in placebo period of 1 month, a very strong placebo effect was observed in this trial: 45% reduction of the attacks between run-in and 4-month treatment period (55% in the OPFA group, P = 0.058). Finally, this large study did not confirm two previous studies based on a small number of patients.
ω-3多不饱和脂肪酸(OPFA)对炎症反应和细胞因子的产生具有有益作用。它们可减少血小板释放5-羟色胺(5HT),并具有血管舒张活性。这使得它们被尝试用于偏头痛的预防性治疗。在经过4周的单盲安慰剂导入期后,患者被随机分组,并在双盲条件下接受安慰剂或每天6克OPFA治疗16周,随后是4周的安慰剂洗脱期。意向性治疗人群包括196名患者。接受全部四个治疗期的患者中,96名服用OPFA,87名服用安慰剂。主要疗效分析是治疗最后4周内偏头痛发作的次数。在此期间,OPFA组的平均发作次数为1.20±1.40,安慰剂组为1.26±1.11(无统计学差异)。研究4个月期间两组的发作总数有显著差异:安慰剂组为7.05次,OPFA组为5.95次(P = 0.036)。两组之间发作的平均强度、平均持续时间和急救药物使用情况无显著差异。除了嗳气方面与OPFA有显著差异外,耐受性良好。尽管有1个月的安慰剂导入期,但在该试验中仍观察到非常强的安慰剂效应:导入期和4个月治疗期之间发作减少了45%(OPFA组为55%,P = 0.058)。最后,这项大型研究并未证实之前两项基于少数患者的研究结果。