Lack of Association Between an Interleukin 1 Beta (IL‐1β) Gene Variation and Refractory Temporal Lobe Epilepsy

Purpose: We attempted to confirm recent findings of Kanemoto et al. that demonstrated a positive association (p < 0.017) between a polymorphism in the promoter region of the interleukin 1‐β (IL‐1β) gene and the clinical phenotype of temporal lobe epilepsy with hippocampal sclerosis (TLE+HS). Meth...

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Veröffentlicht in:Epilepsia (Copenhagen) 2001-06, Vol.42 (6), p.782-784
Hauptverfasser: Buono, Russell J., Ferraro, Thomas N., O'Connor, Michael J., Sperling, Michael R., Ryan, Stephen G., Scattergood, Theresa, Mulholland, Nicole, Gilmore, Joan, Lohoff, Falk W., Berrettini, Wade H.
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Sprache:eng
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Zusammenfassung:Purpose: We attempted to confirm recent findings of Kanemoto et al. that demonstrated a positive association (p < 0.017) between a polymorphism in the promoter region of the interleukin 1‐β (IL‐1β) gene and the clinical phenotype of temporal lobe epilepsy with hippocampal sclerosis (TLE+HS). Methods: We determined the frequency of this polymorphism in a group of 61 TLE+HS patients of European ancestry and compared it with that found in 119 ethnically matched control subjects. Results: Analysis of genotype and allele frequencies showed no statistically significant difference in the distribution of the polymorphism between the two groups (p = 0.10). Conclusions: These data suggest that this IL‐1β promoter polymorphism does not act as a strong susceptibility factor for TLE+HS in a population of individuals of European ancestry.
ISSN:0013-9580
1528-1167
DOI:10.1046/j.1528-1157.2001.42900.x