Spierings Egilius L H, McAllister Peter J, Bilchik Tanya R
Cranio. 2015 Apr;33(2):115-21. doi: 10.1179/0886963414Z.00000000084. Epub 2014 Oct 16.
A review on headache and insomnia revealed that insomnia is a risk factor for increased headache frequency and headache intensity in migraineurs. The authors designed a randomized, double blind, placebo-controlled, parallel-group, pilot study in which migraineurs who also had insomnia were enrolled, to test this observation.
In the study, the authors treated 79 subjects with IHS-II migraine with and/or without aura and with DSM-IV primary insomnia for 6 weeks with 3 mg eszopiclone (Lunesta(®)) or placebo at bedtime. The treatment was preceded by a 2-week baseline period and followed by a 2-week run-out period.
Of the 79 subjects treated, 75 were evaluable, 35 in the eszopiclone group, and 40 in the placebo group. At baseline, the groups were comparable except for sleep latency. Of the three remaining sleep variables, total sleep time, nighttime awakenings, and sleep quality, the number of nighttime awakenings during the 6-week treatment period was significantly lower in the eszopiclone group than in the placebo group (P = 0.03). Of the three daytime variables, alertness, fatigue, and functioning, this was also the case for fatigue (P = 005). The headache variables, frequency, duration, and intensity, did not show a difference from placebo during the 6-week treatment period.
The study did not meet primary endpoint, that is, the difference in total sleep time during the 6-week treatment period between eszopiclone and placebo was less than 40 minutes. Therefore, it failed to answer the question as to whether insomnia is, indeed, a risk factor for increased headache frequency and headache intensity in migraineurs.
一项关于头痛与失眠的综述显示,失眠是偏头痛患者头痛频率增加和头痛强度加大的一个风险因素。作者设计了一项随机、双盲、安慰剂对照、平行组的试点研究,纳入同时患有失眠的偏头痛患者,以验证这一观察结果。
在该研究中,作者使用3毫克艾司佐匹克隆(Lunesta(®))或安慰剂,在睡前对79名患有国际头痛疾病分类(IHS-II)偏头痛伴和/或不伴先兆以及符合《精神疾病诊断与统计手册》第四版(DSM-IV)原发性失眠的受试者进行了为期6周的治疗。治疗前有一个为期2周的基线期,之后是一个为期2周的洗脱期。
在接受治疗的79名受试者中,75名可进行评估,艾司佐匹克隆组35名,安慰剂组40名。在基线时,除睡眠潜伏期外,两组具有可比性。在其余三个睡眠变量,即总睡眠时间、夜间觉醒次数和睡眠质量方面,艾司佐匹克隆组在6周治疗期内的夜间觉醒次数显著低于安慰剂组(P = 0.03)。在三个日间变量,即警觉性、疲劳感和功能方面,疲劳感也是如此(P = 0.05)。在6周治疗期内,头痛变量,即频率、持续时间和强度,与安慰剂相比没有差异。
该研究未达到主要终点,即在6周治疗期内,艾司佐匹克隆与安慰剂之间的总睡眠时间差异小于40分钟。因此,它未能回答失眠是否确实是偏头痛患者头痛频率增加和头痛强度加大的风险因素这一问题。