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.
CITATION STYLE
Buono, R. J., Ferraro, T. N., O’Connor, M. J., Sperling, M. R., Ryan, S. G., Scattergood, T., … Berrettini, W. H. (2001). Lack of association between an interleukin 1 beta (IL-1β gene variation and refractory temporal lobe epilepsy. Epilepsia, 42(6), 782–784. https://doi.org/10.1046/j.1528-1157.2001.42900.x
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