NeuroPain Lab, Lyon Neuroscience Research Centre, CRNL - Inserm U 1028/CNRS UMR 5292, University of Lyon, France; IRISSE Laboratory (EA4075), UFR SHE, University of La Réunion, Le Tampon, France.
NeuroPain Lab, Lyon Neuroscience Research Centre, CRNL - Inserm U 1028/CNRS UMR 5292, University of Lyon, France.
Neurophysiol Clin. 2021 Jun;51(3):209-218. doi: 10.1016/j.neucli.2021.03.001. Epub 2021 Mar 16.
Suppression of alpha and enhancement of gamma electroencephalographic (EEG) power have both been suggested as objective indicators of cortical pain processing. While gamma activity has been emphasized as the best potential marker, its spectral overlap with pain-related muscular responses is a potential drawback. Since muscle contractions are almost universal concomitants of physical pain, here we investigated alpha and gamma scalp-recorded activities during either tonic pain or voluntary facial grimaces mimicking those triggered by pain.
High-density EEG (128 electrodes) was recorded while 14 healthy participants either underwent a cold pressor test (painful hand immersion in 10 °C water) or produced stereotyped facial/nuchal contractions (grimaces) mimicking those evoked by pain. The scalp distribution of spectral EEG changes was quantified via vector-transformation of maps and compared between the pain and grimacing conditions by calculating the cosine of the angle between the two corresponding topographies.
Painful stimuli significantly enhanced gamma power bilaterally in fronto-temporal regions and decreased alpha power in the contralateral central scalp. Sustained cervico-facial contractions (grimaces) gave also rise to significant gamma power increase in fronto-temporal regions but did not decrease central scalp alpha. While changes in alpha topography significantly differed between the pain and grimace situations, the scalp topography of gamma power was statistically indistinguishable from that occurring during grimaces.
Gamma power induced by painful stimuli or voluntary facial-cervical muscle contractions had overlapping topography. Pain-related alpha decrease in contralateral central scalp was less disturbed by muscle activity and may therefore prove more discriminant as an ancillary pain biomarker.
抑制α波并增强γ脑电图(EEG)功率都被认为是皮质疼痛处理的客观指标。虽然γ活动被强调为最佳潜在标志物,但它与疼痛相关肌肉反应的频谱重叠是一个潜在的缺点。由于肌肉收缩几乎是身体疼痛的普遍伴随现象,因此我们在这里研究了在持续疼痛或模拟疼痛引起的面部肌肉收缩时头皮记录的α和γ活动。
14 名健康参与者接受冷加压试验(将手浸入 10°C 水中)或产生模仿疼痛引起的刻板面部/颈部收缩(面部表情)时,记录高密度 EEG(128 个电极)。通过图谱的向量转换来量化频谱 EEG 变化的头皮分布,并通过计算两个对应拓扑之间的角度余弦来比较疼痛和面部表情条件下的余弦。
疼痛刺激显著增加了额颞区的双侧γ波功率,并降低了对侧中央头皮的α波功率。持续的颈面部收缩(面部表情)也导致额颞区γ波功率显著增加,但不会降低中央头皮的α波。虽然α波地形图的变化在疼痛和面部表情情况之间有显著差异,但γ波功率的头皮地形图在统计学上与面部表情时的情况没有区别。
疼痛刺激或自愿面部-颈部肌肉收缩引起的γ波功率具有重叠的拓扑结构。对侧中央头皮与疼痛相关的α波减少受肌肉活动的干扰较小,因此可能更能作为辅助疼痛生物标志物。