Lack of association between an interleukin 1 beta (IL-1β) gene variation and refractory temporal lobe epilepsy

被引:51
作者
Buono, RJ
Ferraro, TN
O'Connor, MJ
Sperling, MR
Ryan, SG
Scattergood, T
Mulholland, N
Gilmore, J
Lohoff, FW
Berrettini, WH
机构
[1] Univ Penn, Sch Med, Dept Psychiat, Ctr Neurobiol & Behav, Philadelphia, PA 19104 USA
[2] Thomas Jefferson Univ, Philadelphia, PA 19107 USA
[3] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[4] Humboldt Univ, Univ Hosp Charite, Berlin, Germany
关键词
temporal lobe epilepsy; human genetics; association study; polymorphism; interleukins;
D O I
10.1046/j.1528-1157.2001.42900.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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-<beta> (IL-1 beta) 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-1 beta promoter polymorphism does not act as a strong susceptibility factor for TLE+HS in a population of individuals of European ancestry.
引用
收藏
页码:782 / 784
页数:3
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