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3D-Neuronavigation In Vivo Through a Patient's Brain During a Spontaneous Migraine Headache
Published on: June 2, 2014
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.
Objective:
To report biphasic changes in cerebral blood flow (CBF) in the acute phase of hemiplegic migraine with prolonged aura (HMPA), in which aura symptoms lasted longer than 24 h, in three patients with familial hemiplegic migraine (FHM) carrying a p.H916L mutation in ATP1A2 gene.
Methods:
We assessed neurovascular changes with time in the affected cerebral hemisphere corresponding to aura symptoms during the acute phase of HMPA. Arterial spin labelling MRI, SPECT for CBF measurement and EEG in three attacks, in one attack FDG-PET measurement for cerebral metabolism was performed. We evaluated CBF at different phases of aura symptoms in 11 attacks of HMPA.
Results:
In two attacks, we found biphasic CBF changes beginning with hypoperfusion followed by persistent hyperperfusion. FDG-PET revealed increased cerebral glucose metabolism in the regions corresponding to hyperperfusion on day 4 when aura symptoms still persisted. In four attacks, Z-score-based CBF mapping revealed multifocal hypoperfusion in the early phase. Hypoperfusion in our study was seen within 19 h of the onset of the symptoms in five of seven attacks, while hyperperfusion was seen 18 h or later in eight of nine attacks. EEG showed attenuated alpha activity without paroxysmal discharge.
Conclusions:
This is the first report showing biphasic CBF changes during the prolonged aura of FHM2. This study suggested that the results of cross-sectional CBF studies should be interpreted carefully. Initial multifocal hypoperfusion is likely due to functional depression of multifocal origin in the affected hemisphere, but the mechanism of persistent hyperperfusion requires further investigation.
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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