4.3 Article

Migraine Type-Dependent Patterns of Brain Activation After Facial and Intranasal Trigeminal Stimulation

Journal

BRAIN TOPOGRAPHY
Volume 36, Issue 1, Pages 52-71

Publisher

SPRINGER
DOI: 10.1007/s10548-022-00924-x

Keywords

Headache; Clustering analysis; EEG; Pain; Odor; Nose

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This study investigates the alterations in trigeminal activation in migraine using EEG-derived event-related potentials (ERP). The results reveal changes in trigeminal-sensory response patterns in different brain regions in migraine patients, which are correlated with clinical characteristics and disease duration. The study also identifies specific trigeminal responses in patients with aura. These findings suggest the presence of dysfunctional central pain processing in migraine and indicate that EEG patterns can serve as biomarkers for the condition.
In migraine, the trigeminal nerve is intimately involved in the pathophysiology of the disease. We hypothesized that alterations in the sensory trigeminal activation in migraine would be reflected by EEG-derived event-related potentials (ERP). We aimed to investigate differences in the temporal and spatial processing of trigeminal stimuli between interictal migraine patients and healthy subjects. ERP to trigeminal stimuli were recorded at 128-channels to allow localization of their cortical sources with high temporal resolution. Seventeen patients with episodic migraine without aura, 17 subjects with episodic migraine with aura, and 17 healthy subjects participated in the study. The first branch of the trigeminal nerve was stimulated using intranasal chemical (CO2), cutaneous electrical, and cutaneous mechanical (air puff) stimuli. Analyses were performed with regard to micro-state segmentation, ERP source localization, and correlation with the patients' clinical characteristics. Topographical assessments of EEG configurations were associated with the pathological condition. The source analysis revealed altered trigeminal-sensory response patterns in the precuneus, temporal pole, and cerebellum for both migraine groups during the interictal phase. The estimated current source density was positively correlated with migraine disease duration, indicating brain functional and structural changes as a consequence of the disease. Hyperactivity of the cerebellar posterior lobe was observed as a specific trigeminal response of migraine patients with aura. In conclusion, our results suggest the presence of brain changes accompanying the advancement of migraine as an expression of dysfunctional central pain processing. Hence, we identified EEG patterns in response to mechano-/chemosensory stimuli that can serve as biomarkers of migraine.

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