A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy

被引:88
作者
Stogmann, E
Zimprich, A
Baumgartner, C
Aull-Watschinger, S
Höllt, V
Zimprich, F
机构
[1] Univ Hosp Vienna, Dept Neurol, A-1090 Vienna, Austria
[2] Univ Munich, Klinikum Grosshadern, Dept Neurol, Munich, Germany
[3] Otto Von Guericke Univ, Inst Pharmacol & Toxicol, Magdeburg, Germany
关键词
D O I
10.1002/ana.10108
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The prodynorphin gene (PDYN) encoding the anticonvulsant peptide dynorphin is a strong candidate for a seizure suppressor gene and thus a possible modulator of susceptibility to temporal lobe epilepsy. We performed a case control association study in 155 patients with nonlesional temporal lobe epilepsy and 202 controls and found that PDYN promotor low-expression L-alleles confer an increased risk for temporal lobe epilepsy in patients with a family history for seizures. Irrespective of the familial background, L-homozygotes display a higher risk for secondarily generalized seizures and status epilepticus.
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页码:260 / 263
页数:4
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