Biphasic neurovascular changes in prolonged migraine aura in familial hemiplegic migraine type 2

Takahiro Iizuka1, Naomi Tominaga1, Juntaro Kaneko1

  • 1Department of Neurology, Kitasato University School of Medicine, Sagamihara, Japan.

Abstract

Insights

Familial hemiplegic migraine with prolonged aura (HMPA) shows biphasic cerebral blood flow (CBF) changes, starting with hypoperfusion then hyperperfusion. This finding offers new insights into FHM2 aura mechanisms.

Area of Science:

  • Neuroscience
  • Medical Imaging
  • Genetics

Background:

  • Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura.
  • Prolonged aura (HMPA) symptoms lasting over 24 hours present unique diagnostic challenges.
  • Genetic mutations, such as in the ATP1A2 gene (FHM2), are implicated in FHM pathogenesis.

Observation:

  • This study investigated neurovascular changes during acute HMPA in three FHM2 patients with the p.H916L ATP1A2 mutation.
  • Cerebral blood flow (CBF) was assessed using arterial spin labelling MRI, SPECT, and FDG-PET.
  • Electroencephalography (EEG) was also performed to evaluate brain activity.

Findings:

  • Biphasic CBF changes were observed, characterized by initial hypoperfusion followed by persistent hyperperfusion.
  • Multifocal hypoperfusion occurred in the early phase (within 19 hours), while hyperperfusion was noted later (18+ hours).
  • FDG-PET revealed increased cerebral glucose metabolism in hyperperfused regions during persistent aura symptoms.

Implications:

  • This is the first report of biphasic CBF changes in prolonged aura associated with FHM2.
  • Findings suggest that cross-sectional CBF studies in HMPA require careful interpretation due to dynamic changes.
  • The mechanism of persistent hyperperfusion warrants further investigation to understand FHM2 pathophysiology.

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