- 作者：Kjell Heusera ; kjell.heuser@oslo-universitetssykehus.no ; dr.heuser@gmail.com ; Milada Cvancarovab ; Leif Gjerstada ; c ; Erik Taubø ; lla ; c
- 关键词：Temporal Lobe Epilepsy ; Hippocampal sclerosis ; Mesial Temporal Lobe Epilepsy ; Febrile seizures ; Phenotype
- 刊名：Seizure
- 出版年：2011
- 出版时间：March 2011
- 年：2011
- 卷：20
- 期：2
- 页码：163-166
- 全文大小：131 K
ObjectivePharmacoresistance continues to be a major challenge in Temporal Lobe Epilepsies (TLE). A key to overcome pharmacoresistance is to identify subgroups among the TLE and disclose their specific molecular pathways. This will facilitate a tailored pharmacological treatment and improve outcome. There is growing evidence in favor of the theory that TLE with childhood febrile seizures (TLE-FS) may represent one distinctive subgroup among the TLE.Material and methods
We compared clinical features from 102 TLE-FS patients with 105 TLE patients without FS. We also conducted a logistic regression analysis to adjust for possible confounders caused by overrepresentation of patients with Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis (MTLE-HS) in the TLE-FS group.
Results
MTLE-HS was overrepresented in patients with TLE-FS (p = 0.043). Age at epilepsy onset was lower in patients with TLE-FS (p < 0.001). TLE-FS patients had a higher frequency of first grade family members with FS (p = 0.003, adjusted for MTLE-HS: p = 0.002). They were more frequently plagued with simple partial seizures (p = 0.015, adjusted: p = 0.038), and especially with vertiginous symptoms (p = 0.004 adjusted: p = 0.006). They also had the higher frequency of autonomic symptoms (p = 0.003; adjusted: p = 0.012), and more generalized tonic–clonic seizures (0.034; adjusted p = 0.038).
Conclusion
We identified TLE-FS as a phenotype that can be delineated from other TLE. None of the characteristics are specific, but we disclosed a set of features also when adjusted for MTLE-HS.