Early epileptiform EEG activity in infants with tuberous sclerosis complex predicts epilepsy and neurodevelopmental outcomes

被引:23
|
作者
De Ridder, Jessie [1 ]
Verhelle, Birgit [1 ]
Vervisch, Jan [1 ]
Lemmens, Katrien [1 ]
Kotulska, Katarzyna [2 ]
Moavero, Romina [3 ,4 ]
Curatolo, Paolo [3 ]
Weschke, Bernhard [5 ]
Riney, Kate [6 ,7 ]
Feucht, Martha [8 ]
Krsek, Pavel [9 ]
Nabbout, Rima [10 ]
Jansen, Anna C. [11 ]
Wojdan, Konrad [12 ,13 ]
Domanska-Pakiela, Dorota [2 ]
Kaczorowska-Frontczak, Magdalena [2 ]
Hertzberg, Christoph [14 ]
Ferrier, Cyrille H. [15 ]
Samueli, Sharon [8 ]
Benova, Barbora [9 ]
Aronica, Eleonora [16 ,17 ]
Kwiatkowski, David J. [18 ]
Jansen, Floor E. [15 ]
Jozwiak, Sergiusz [2 ,19 ]
Lagae, Lieven [1 ]
机构
[1] Katholieke Univ Leuven, Dept Dev & Regenerat, Sect Pediat Neurol, KU Leuven, Leuven, Belgium
[2] Childrens Mem Hlth Inst, Dept Neurol & Epileptol, Warsaw, Poland
[3] Tor Vergata Univ, Syst Med Dept, Child Neurol & Psychiat Unit, Rome, Italy
[4] Bambino Gesu Pediat Hosp, Neurosci & Neurorehabil Dept, Child Neurol Unit, Rome, Italy
[5] Charite Univ Med Berlin, Dept Child Neurol, Berlin, Germany
[6] Queensland Childrens Hosp, Neurosci Unit, Brisbane, Qld, Australia
[7] Univ Queensland, Sch Clin Med, Brisbane, Qld, Australia
[8] Med Univ Vienna, Dept Pediat, Vienna, Austria
[9] Charles Univ Prague, Motol Univ Hosp, Fac Med 2, Dept Paediat Neurol, Prague, Czech Republic
[10] Univ Paris 05, Necker Enfants Malad Hosp, Reference Ctr Rare Epilepsies, Imagine Inst,Dept Pediat Neurol,INSERM U1163, Paris, France
[11] Univ Hosp Brussel, Pediat Neurol Unit, Brussels, Belgium
[12] Transit Technol, Warsaw, Poland
[13] Warsaw Univ & Technol, Inst Heat Engn, Warsaw, Poland
[14] Vivantes Klinikum Neukoln, Diag & Behandlungszentrum Kinder & Jugendl, Berlin, Germany
[15] Univ Med Ctr Utrecht, Brain Ctr, Dept Child Neurol, Utrecht, Netherlands
[16] Univ Amsterdam, Amsterdam Univ Med Ctr UMC, Dept Neuro Pathol, Amsterdam, Netherlands
[17] Stichting Epilepsie Instellingen Nederland SEIN, Zwolle, Netherlands
[18] Harvard Med Sch, Brigham & Womens Hosp, Boston, MA USA
[19] Med Univ Warsaw, Dept Child Neurol, Warsaw, Poland
基金
欧盟第七框架计划;
关键词
EEG; epilepsy; epileptogenesis; neurodevelopment; tuberous sclerosis complex; DRUG-RESISTANT EPILEPSY; IMPENDING EPILEPSY; ONSET; SEIZURES;
D O I
10.1111/epi.16892
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To study the association between timing and characteristics of the first electroencephalography (EEG) with epileptiform discharges (ED-EEG) and epilepsy and neurodevelopment at 24 months in infants with tuberous sclerosis complex (TSC). Methods Patients enrolled in the prospective Epileptogenesis in a genetic model of epilepsy - Tuberous sclerosis complex (EPISTOP) trial, had serial EEG monitoring until the age of 24 months. The timing and characteristics of the first ED-EEG were studied in relation to clinical outcome. Epilepsy-related outcomes were analyzed separately in a conventionally followed group (initiation of vigabatrin after seizure onset) and a preventive group (initiation of vigabatrin before seizures, but after appearance of interictal epileptiform discharges [IEDs]). Results Eighty-three infants with TSC were enrolled at a median age of 28 days (interquartile range [IQR] 14-54). Seventy-nine of 83 patients (95%) developed epileptiform discharges at a median age of 77 days (IQR 23-111). Patients with a pathogenic TSC2 variant were significantly younger (P-value .009) at first ED-EEG and more frequently had multifocal IED (P-value .042) than patients with a pathogenic TSC1 variant. A younger age at first ED-EEG was significantly associated with lower cognitive (P-value .010), language (P-value .001), and motor (P-value .013) developmental quotients at 24 months. In the conventional group, 48 of 60 developed seizures. In this group, the presence of focal slowing on the first ED-EEG was predictive of earlier seizure onset (P-value .030). Earlier recording of epileptiform discharges (P-value .019), especially when multifocal (P-value .026) was associated with higher risk of drug-resistant epilepsy. In the preventive group, timing, distribution of IED, or focal slowing, was not associated with the epilepsy outcomes. However, when multifocal IEDs were present on the first ED-EEG, preventive treatment delayed the onset of seizures significantly (P-value <.001). Significance Early EEG findings help to identify TSC infants at risk of severe epilepsy and neurodevelopmental delay and those who may benefit from preventive treatment with vigabatrin.
引用
收藏
页码:1208 / 1219
页数:12
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