1 Danish Headache Centre, Department of Neurology, Rigshospitalet, Faculty of Health and Medical Sciences, University of Copenhagen, DK-2600 Glostrup, Denmark.
2 Functional Imaging Unit, Department of Clinical Physiology, Nuclear Medicine and PET, Rigshospitalet, Faculty of Health and Medical Sciences, University of Copenhagen, DK-2600 Glostrup, Denmark.
Brain. 2016 Mar;139(Pt 3):723-37. doi: 10.1093/brain/awv359. Epub 2015 Dec 16.
Migraine with aura is prevalent in high-altitude populations suggesting an association between migraine aura and hypoxia. We investigated whether experimental hypoxia triggers migraine and aura attacks in patients suffering from migraine with aura. We also investigated the metabolic and vascular response to hypoxia. In a randomized double-blind crossover study design, 15 migraine with aura patients were exposed to 180 min of normobaric hypoxia (capillary oxygen saturation 70-75%) or sham on two separate days and 14 healthy controls were exposed to hypoxia. Glutamate and lactate concentrations in the visual cortex were measured by proton magnetic resonance spectroscopy. The circumference of cranial arteries was measured by 3 T high-resolution magnetic resonance angiography. Hypoxia induced migraine-like attacks in eight patients compared to one patient after sham (P = 0.039), aura in three and possible aura in 4 of 15 patients. Hypoxia did not change glutamate concentration in the visual cortex compared to sham, but increased lactate concentration (P = 0.028) and circumference of the cranial arteries (P < 0.05). We found no difference in the metabolic or vascular responses to hypoxia between migraine patients and controls. In conclusion, hypoxia induced migraine-like attacks with and without aura and dilated the cranial arteries in patients with migraine with aura. Hypoxia-induced attacks were not associated with altered concentration of glutamate or other metabolites. The present study suggests that hypoxia may provoke migraine headache and aura symptoms in some patients. The mechanisms behind the migraine-inducing effect of hypoxia should be further investigated.
偏头痛伴先兆在高海拔人群中较为常见,提示偏头痛先兆与低氧之间存在关联。我们研究了实验性低氧是否会引发偏头痛伴先兆患者的偏头痛和先兆发作。我们还研究了低氧对代谢和血管的反应。在一项随机、双盲、交叉研究设计中,15 名偏头痛伴先兆患者在两天内分别暴露于常压低氧(毛细血管氧饱和度 70-75%)或假处理下 180 分钟,14 名健康对照者暴露于低氧下。通过质子磁共振波谱测量视觉皮层中的谷氨酸和乳酸浓度。通过 3T 高分辨率磁共振血管造影测量颅动脉周长。与假处理相比,低氧引起了 8 名患者偏头痛样发作(P = 0.039),3 名患者出现先兆,15 名患者中有 4 名可能出现先兆。与假处理相比,低氧并未改变视觉皮层中的谷氨酸浓度,但增加了乳酸浓度(P = 0.028)和颅动脉周长(P < 0.05)。我们没有发现偏头痛患者和对照组对低氧的代谢或血管反应有差异。总之,低氧引起了偏头痛伴先兆患者的偏头痛样发作和先兆发作,并扩张了颅动脉。低氧诱导的发作与谷氨酸或其他代谢物浓度的改变无关。本研究表明,低氧可能会引发一些患者的偏头痛头痛和先兆症状。低氧诱导偏头痛的机制应进一步研究。