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Published online before print March 26, 2009, 10.1183/09031936.00179008
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Eur Respir J 2009; 34:882-887
Copyright ©ERS Journals Ltd 2009

Pulmonary arteriovenous malformations associated with migraine with aura

M. C. Post1, M. W. F. van Gent1, H. W. M. Plokker1, C. J. J. Westermann2, J. C. Kelder1, J. J. Mager2, T. T. Overtoom3, W. J. Schonewille4, V. Thijs5,6 and R. J. Snijder2

Depts of 1 Cardiology, 2 Pulmonology, 3 Radiology, and 4 Neurology, St Antonius Hospital, Nieuwegein, The Netherlands. 5 Dept of Neurology, University Hospital Gasthuisberg, and 6 Vesalius Research Center, Leuven, Belgium.

CORRESPONDENCE: M. C. Post, Dept of Cardiology, St Antonius Hospital, Koekoekslaan 1, 3435CM Nieuwegein, The Netherlands. E-mail: m.post{at}antonius.net

Keywords: Hereditary haemorrhagic telangiectasia, migraine, shunt

Received: November 25, 2008
Accepted March 16, 2009

Migraine with aura (MA) is associated with cardiac right-to-left shunt. We prospectively studied the association between pulmonary arteriovenous malformations (PAVMs) and MA in hereditary haemorrhagic telangiectasia (HHT).

All 220 consecutive HHT patients who underwent high-resolution chest computed tomography for PAVM screening were included prospectively. Prior to screening, a structured validated headache questionnaire was completed by 196 patients (57% female; mean±sd age 44.6±15.2 yrs). Two neurologists diagnosed migraine according to the International Headache Society Criteria.

A PAVM was present in 70 (36%) patients. The prevalence of MA was 24% in the presence of a PAVM compared with 6% in the absence of a PAVM (OR 4.6, 95% CI 1.84–11.2; p = 0.001), and MA was an independent predictor for the presence of PAVM using multivariate analysis (OR 3.6, 95% CI 1.21–10.5; p = 0.02). A PAVM was present in 68% of the patients with MA compared with 32% in the non-migraine controls (OR 4.6, 95% CI 1.84–11.2; p = 0.001), and a PAVM was an independent predictor for MA using multivariate analysis (OR 3.0, 95% CI 1.00–9.20; p = 0.05).

In conclusion, PAVMs are associated with MA in HHT patients.







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