From the Research and Innovation (R&I) Company, Padova, Italy (Drs. Lisi, Terrazzino, Leon, and Miccichè, Stecca); Department of Pediatrics, University of Padua, Italy (Garbo, Drs. Battistella, Franzoi, Tripoli, Clementi); and IRCCS St. Camillo Hospital, Venice, Italy (Dr. Leon).
Endothelin Receptor A –231 G>A Polymorphism: No Linkage to Primary Pediatric Headache
Version of Record online: 21 MAR 2006
Headache: The Journal of Head and Face Pain
Volume 46, Issue 3, pages 486–491, March 2006
How to Cite
Lisi, V., Garbo, G., Battistella, P., Miccichè, F., Stecca, A., Terrazzino, S., Franzoi, M., Tripoli, E., Leon, A. and Clementi, M. (2006), Endothelin Receptor A –231 G>A Polymorphism: No Linkage to Primary Pediatric Headache. Headache: The Journal of Head and Face Pain, 46: 486–491. doi: 10.1111/j.1526-4610.2006.00380.x
- Issue online: 21 MAR 2006
- Version of Record online: 21 MAR 2006
- Accepted for publication November 29, 2005.
- primary pediatric headache;
- endothelin type A;
- tension-type headache
Objective.—To assess whether the biallelic –231 G>A polymorphism of the endothelin type A receptor (EDNRA) gene, previously shown to be a marker of increased risk for developing migraine, has a role in the susceptibility to primary pediatric headache.
Background.—Several studies suggest that endothelin has a role in migraine. A recent association study has shown that the biallelic –231 G>A polymorphism of the EDNRA gene is associated to migraine in an elderly population.
Methods.—A total of 126 consecutive unrelated pediatric patients affected by primary headache, classified according to the International Headache Society criteria in migraine (migraine with aura, n = 3; migraine without aura, n = 80), and tension-type headache (episodic tension-type headache, n = 36; chronic tension-type headache, n = 7) patients, were recruited to the study. Sixty-seven healthy blood donors were used as a control group. Genomic DNA was extracted from buccal swabs or blood samples and analyzed by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) for the above-mentioned polymorphism. Allele and genotype frequencies for primary headache patients were analyzed in comparison with the control group.
Results.—No significant differences were found in the distribution of the EDNRA –231 G>A polymorphic variant when considering both genotype (migraine χ2= 2.78, P= .25; tension-type headache χ2= 3.58, P= .17) and allelic frequencies (migraine χ2= 1.48, P= .22; tension-type headache χ2= 0.39, P= .56). Furthermore, no significant genotype-related difference was found in relation to clinical features, such as age at onset, frequency, and length of the attacks.
Conclusions.—Our study shows that the –231 G>A polymorphism in the EDNRA gene is neither associated with primary juvenile headache nor significantly correlated with main clinical features characteristic of the headache pathology in pediatric settings.