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May 22, 2001; 56 (10) Expedited Articles

Association between migraine and endothelin type A receptor (ETA −231 A/G) gene polymorphism

C. Tzourio, M. El Amrani, O. Poirier, V. Nicaud, M.-G. Bousser, A. Alpérovitch
First published May 22, 2001, DOI: https://doi.org/10.1212/WNL.56.10.1273
C. Tzourio
MD, PhD
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M. El Amrani
MD
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O. Poirier
PhD
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V. Nicaud
MA
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M.-G. Bousser
MD
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A. Alpérovitch
MD, MSc
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Citation
Association between migraine and endothelin type A receptor (ETA −231 A/G) gene polymorphism
C. Tzourio, M. El Amrani, O. Poirier, V. Nicaud, M.-G. Bousser, A. Alpérovitch
Neurology May 2001, 56 (10) 1273-1277; DOI: 10.1212/WNL.56.10.1273

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Abstract

Background: Previous studies have described an association between migraine and endothelin, a potent vasoconstrictor.

Objective: To test the association between migraine and gene polymorphisms of the endothelin system.

Methods: A population-based study of elderly individuals (n = 1,188) in Nantes (western France) was conducted. Lifetime migraine was defined according to the International Headache Society criteria, after an interview with a headache specialist. Five polymorphisms in genes encoding endothelin 1, endothelin type A (ETA), and type B receptors were determined in more than 90% of the sample.

Results Migraine was diagnosed in 140 participants (11.9%). The ETA (−231 A/G) polymorphism was the only polymorphism significantly associated with migraine. There was a trend of decreasing prevalence of migraine with number of copies of the G allele (AA genotype: 15.7% of participants with migraine, AG: 9.7%, GG: 2.9%; p < 0.001). Carrying the G allele was associated with a sex- and age-adjusted odds ratio of 0.50 (95% CI, 0.34 to 0.74). The association was observed in both sexes and was stronger in participants with a family history of severe headaches than in those without. Conclusions: A variant of the ETA receptor gene modulates the risk for migraine. These results offer new insights into the pathophysiology of the vascular component of migraine.

  • Received January 23, 2001.
  • Accepted March 15, 2001.
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