Previous studies have demonstrated that structural and functional abnormalities in episodic migraine, less is known about altered brain perfusion in the EM
The image processing included following steps: The structural images were segmented into grayand white matter tissue probability maps using DARTEL methods, which simultaneously generated the normalized T1 tissue probabilitymaps; All the T1-TPM wereused to generate average T1-TPM and further generate brain mask; The individual cerebral blood flow maps were spatially normalize into strandard Montreal Neurologic Institute stereotaxic space by coregistering with the individual T1-TPM and resampled into 1.5 × 1.5 × 1.5 mm3 isotropic size, which would generated individual normalized CBF maps; The individual nCBF maps were warped by the brain mask to extract brain tissue; The individual normalized CBF maps with brain extractionwere performed Z transformation to avoid individual hemodynamic variation, and spatially smoothed with a 6-mm isotropic Gaussian kernel
Comparison of gray matter perfusion between EM and normal controls The brain region with increased perfusion located in the left Brodmann 38
In conclusion, this study revealed that the interictal hyperperfusion in left temporal pole and vlPFC may reflect the neural metabolism abnormality regarding multi-dimensional pain processing in migraine
The pattern of cerebral hyperperfusion at interictal migraine may elucidate the neurogenic mechanism in the EM genesis. 3D 3D pseudo-continuous arterial spin labeling technique would non-invasively provide valuable cerebral perfusion information for the further pathophysiological and neuropsychological study in EM