Altered functional magnetic resonance imaging resting‐state connectivity in periaqueductal gray networks in migraine

导水管周围灰质 神经科学 偏头痛 静息状态功能磁共振成像 痛觉超敏 功能磁共振成像 发作性 体感系统 心理学 伤害 扣带回前部 医学 麻醉 脑电图 痛觉过敏 中枢神经系统 内科学 中脑 认知 受体
作者
Caterina Mainero,Jasmine Boshyan,Nouchine Hadjikhani
出处
期刊:Annals of Neurology [Wiley]
卷期号:70 (5): 838-845 被引量:369
标识
DOI:10.1002/ana.22537
摘要

Abstract Objective: The periaqueductal gray matter (PAG), a known modulator of somatic pain transmission, shows evidence of interictal functional and structural abnormalities in migraineurs, which may contribute to hyperexcitability along spinal and trigeminal nociceptive pathways, and lead to the migraine attack. The aim of this study was to examine functional connectivity of the PAG in migraine. Methods: Using resting‐state functional MRI, we compared functional connectivity between PAG and a subset of brain areas involved in nociceptive/somatosensory processing and pain modulation in 17 subjects with migraine, during a pain‐free state, versus 17 gender‐ and age‐matched controls. We also assessed the relation between intrinsic resting‐state correlations within PAG networks and the average monthly frequency of migraine attacks, as well as allodynia. Results: Our findings show stronger connectivity between the PAG and several brain areas within nociceptive and somatosensory processing pathways in migraineurs versus controls. In addition, as the monthly frequency of migraine attacks worsens, the strength of the connectivity in some areas within these pathways increases, whereas a significant decrease in functional resting‐state connectivity between the PAG and brain regions with a predominant role in pain modulation (prefrontal cortex, anterior cingulate, amygdala) can be evidenced. Finally, migraineurs with a history of allodynia exhibit significantly reduced connectivity between PAG, prefrontal regions, and anterior cingulate compared to migraineurs without allodynia. Interpretation: These data reveal interictal dysfunctional dynamics within pain pathways in migraine manifested as an impairment of the descending pain modulatory circuits, likely leading to loss of pain inhibition, and hyperexcitability primarily in nociceptive areas. ANN NEUROL 2011
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