Volume 26, Issue 8 pp. 925-933

Dipyridamole may induce migraine in patients with migraine without aura

C Kruuse

C Kruuse

Danish Headache Centre and Department of Neurology, University of Copenhagen, Glostrup Hospital, Copenhagen, Denmark

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LH Lassen

LH Lassen

Danish Headache Centre and Department of Neurology, University of Copenhagen, Glostrup Hospital, Copenhagen, Denmark

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HK Iversen

HK Iversen

Danish Headache Centre and Department of Neurology, University of Copenhagen, Glostrup Hospital, Copenhagen, Denmark

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S Oestergaard

S Oestergaard

Danish Headache Centre and Department of Neurology, University of Copenhagen, Glostrup Hospital, Copenhagen, Denmark

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J Olesen

J Olesen

Danish Headache Centre and Department of Neurology, University of Copenhagen, Glostrup Hospital, Copenhagen, Denmark

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First published: 17 July 2006
Citations: 6
C. Kruuse MD, PhD, Danish Headache Centre and Department of Neurology, Glostrup Hospital, University of Copenhagen, DK-2600 Glostrup, Copenhagen, Denmark. Tel. + 45 4323 2796, fax + 45 4323 3839, e-mail [email protected] Received 8 July 2005, accepted 16 December 2005

Abstract

Dipyridamole inhibits phosphodiesterase 5 (PDE5) and adenosine re-uptake. The most prominent side-effect is headache. We examined the migraine-generating effects of dipyridamole as well as the cerebral blood velocity response in a single-blind study, including 10 patients with migraine without aura and 10 healthy subjects. Dipyridamole 0.142 mg/kg per min was administered intravenously. Headache intensity was scored on a verbal rating scale along with pain characteristics and accompanying symptoms. Blood velocity in the middle cerebral artery (Vmca), blood pressure and heart rate were recorded repeatedly. Headache was induced in all migraine patients and in eight of 10 healthy subjects (P = 0.47) with no significant difference in headache intensity (P = 0.53). However, five patients but only one healthy subject experienced the symptoms of migraine without aura, according to ICHD-2 criteria, within 12 h (P = 0.14). Four patients reported photophobia after dipyridamole compared with no healthy subjects (P = 0.087). Vmca decreased (P < 0.001) during and after dipyridamole infusion with no difference between groups (P = 0.15) coinciding with initiation, but not cessation of immediate headache. Thus, dipyridamole induces symptoms of migraine and an initial decrease in Vmca in migraine patients, but not significantly more than in healthy subjects. This relatively low frequency of migraine induction, compared with nitric oxide donors and sildenafil, is probably due to the less specific action of dipyridamole on the cGMP signalling pathway as well as a possible bidirectional effect of adenosine on migraine induction.

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