Lack of Association Between an Interleukin 1 Beta (IL-1β) Gene Variation and Refractory Temporal Lobe Epilepsy
Version of Record online: 20 DEC 2001
Volume 42, Issue 6, pages 782–784, June 2001
How to Cite
Buono, R. J., Ferraro, T. N., O'Connor, M. J., Sperling, M. R., Ryan, S. G., Scattergood, T., Mulholland, N., Gilmore, J., Lohoff, F. W. and Berrettini, W. H. (2001), Lack of Association Between an Interleukin 1 Beta (IL-1β) Gene Variation and Refractory Temporal Lobe Epilepsy. Epilepsia, 42: 782–784. doi: 10.1046/j.1528-1157.2001.42900.x
- Issue online: 20 DEC 2001
- Version of Record online: 20 DEC 2001
- Accepted March 9, 2001.
- Temporal lobe epilepsy;
- Human genetics;
- Association study;
Summary: 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.