antithrombotic treatment for migraine in patients with patent foramen ovale
Patent foramen ovale (PFO) is a remnant of the fetal circulation (1,2):
- foramen ovale is a channel between the left and right atria of the heart during the embryonic period
- under normal physiological conditions, the foramen ovale will close in the first year after birth
- if it is not closed after three years of age, it is termed as patent foramen ovale (PFO)
- about 20-30% of adults have an incomplete fusion of the fossa, which is a permanent slit-like interatrial opening
- usually, the blood pressure of the left atrium is higher than that of the right atrium, which will not cause right-to-left shunt
- under normal physiological conditions, the foramen ovale will close in the first year after birth
- multiple studies suggest that migraine is more prevalent in subjects with PFO and vice versa
- PFO is associated with migraine, particularly migraine with aura, and been shown observationally to involve a possible microembolic mechanism
- antiplatelet treatment (eg, aspirin or P2Y12 inhibitors) has shown potential benefit in small studies
In a study to evaluate the efficacy and safety of antithrombotic treatment for migraine prevention in participants with PFO (2):
- for responder rate in patients with PFO and migraine, all three antithrombotic agents (aspirin, clopidogrel, and rivaroxaban) were non-inferior to metoprolol in reducing monthly migraine days or attacks by ≥50%
- rivaroxaban showed a higher responder rate than metoprolol
- showed superior responder rates over metoprolol without an increase in major bleeding events
- findings suggest a potential microembolic mechanism contributes to migraine in patients with PFO
Reference:
- Liu K, Wang BZ, Hao Y, Song S, Pan M. The Correlation Between Migraine and Patent Foramen Ovale. Front Neurol. 2020 Dec 1;11:543485.
- Li Z et al. Antithrombotic treatment for migraine in patients with patent foramen ovale: multicentre, randomised, active controlled, open label trial.BMJ 2026; 394 :e100103.
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