The concept of disease modification

被引:10
作者
Cross, J. Helen [1 ]
Lagae, Lieven [2 ]
机构
[1] UCL NIHR BRC Great Ormond St Inst Child Hlth, London WC1N 1EH, England
[2] Univ Hosp Leuven, Paediat Neurol, Herestr 49, B-3000 Leuven, BE, Belgium
关键词
Disease modification; Epilepsy; Epileptic encephalopathy; ONSET; LAMOTRIGINE;
D O I
10.1016/j.ejpn.2019.12.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Traditionally treatment of epileptic seizures has been symptomatic, namely medication has been targeted at raising the threshold to the occurrence of epileptic seizures. This has had little impact on the rate of drug resistance over time, or impact on comorbidities such as learning and behaviour particularly in the early onset epilepsies. The advent of advanced neuroimaging and genomics has revealed the cause of the epilepsy in a much higher percentage, and advanced our knowledge as to the underlying pathophysiology. This has given us the opportunity to turn to the possibility of interventional treatment, targeting the underlying cause, and consequently the possibility of changing the natural history of disease. Here we review the options open to us, and the evidence to date. (C) 2019 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:43 / 46
页数:4
相关论文
共 21 条
[1]  
[Anonymous], EPISTOP EPIMARKER IE
[2]   Pediatric epilepsy surgery: the earlier the better [J].
Braun, Kees P. J. ;
Cross, J. Helen .
EXPERT REVIEW OF NEUROTHERAPEUTICS, 2018, 18 (04) :261-263
[3]   Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology [J].
Catarino, Claudia B. ;
Liu, Joan Y. W. ;
Liagkouras, Ioannis ;
Gibbons, Vaneesha S. ;
Labrum, Robyn W. ;
Ellis, Rachael ;
Woodward, Cathy ;
Davis, Mary B. ;
Smith, Shelagh J. ;
Cross, J. Helen ;
Appleton, Richard E. ;
Yendle, Simone C. ;
McMahon, Jacinta M. ;
Bellows, Susannah T. ;
Jacques, Thomas S. ;
Zuberi, Sameer M. ;
Koepp, Matthias J. ;
Martinian, Lillian ;
Scheffer, Ingrid E. ;
Thom, Maria ;
Sisodiya, Sanjay M. .
BRAIN, 2011, 134 :2982-3010
[4]   Novel therapeutic approaches for disease-modification of epileptogenesis for curing epilepsy [J].
Clossen, Bryan L. ;
Reddy, Doodipala Samba .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2017, 1863 (06) :1519-1538
[5]   Lamotrigine can be beneficial in patients with Dravet syndrome [J].
Dalic, Linda ;
Mullen, Saul A. ;
Perez, Eliane Roulet ;
Scheffer, Ingrid .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2015, 57 (02) :200-202
[6]   Influence of contraindicated medication use on cognitive outcome in Dravet syndrome and age at first afebrile seizure as a clinical predictor in SCN1A-related seizure phenotypes [J].
de Lange, Iris M. ;
Gunning, Boudewijn ;
Sonsma, Anja C. M. ;
van Gemert, Lisette ;
van Kempen, Marjan ;
Verbeek, Nienke E. ;
Nicolai, Joost ;
Knoers, Nine V. A. M. ;
Koeleman, Bobby P. C. ;
Brilstra, Eva H. .
EPILEPSIA, 2018, 59 (06) :1154-1165
[7]   Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy [J].
Finkel, R. S. ;
Mercuri, E. ;
Darras, B. T. ;
Connolly, A. M. ;
Kuntz, N. L. ;
Kirschner, J. ;
Chiriboga, C. A. ;
Saito, K. ;
Servais, L. ;
Tizzano, E. ;
Topaloglu, H. ;
Tulinius, M. ;
Montes, J. ;
Glanzman, A. M. ;
Bishop, K. ;
Zhong, Z. J. ;
Gheuens, S. ;
Bennett, C. F. ;
Schneider, E. ;
Farwell, W. ;
De Vivo, D. C. .
NEW ENGLAND JOURNAL OF MEDICINE, 2017, 377 (18) :1723-1732
[8]   Adjunctive everolimus therapy for treatment-resistant focal-onset seizures associated with tuberous sclerosis (EXIST-3): a phase 3, randomised, double-blind, placebo-controlled study [J].
French, Jacqueline A. ;
Lawson, John A. ;
Yapici, Zuhal ;
Ikeda, Hiroko ;
Polster, Tilman ;
Nobbout, Rima ;
Curatolo, Paolo ;
de Vries, Petrus J. ;
Diugos, Dennis J. ;
Berkowitz, Noah ;
Voi, Maurizio ;
Peyrard, Severine ;
Pelov, Diana ;
Franz, David N. .
LANCET, 2016, 388 (10056) :2153-2163
[9]   Lamotrigine and seizure aggravation in severe myoclonic epilepsy [J].
Guerrini, R ;
Dravet, C ;
Genton, P ;
Belmonte, A ;
Kaminska, A ;
Dulac, O .
EPILEPSIA, 1998, 39 (05) :508-512
[10]   Antiepileptic treatment before the onset of seizures reduces epilepsy severity and risk of mental retardation in infants with tuberous sclerosis complex [J].
Jozwiak, Sergiusz ;
Kotulska, Katarzyna ;
Domanska-Pakiela, Dorota ;
Lojszczyk, Barbara ;
Syczewska, Malgorzata ;
Chmielewski, Dariusz ;
Dunin-Wasowicz, Dorota ;
Kmiec, Tomasz ;
Szymkiewicz-Dangel, Joanna ;
Kornacka, Maria ;
Kawalec, Wanda ;
Kuczynski, Dariusz ;
Borkowska, Julita ;
Tomaszek, Katarzyna ;
Jurkiewicz, Elzbieta ;
Respondek-Liberska, Maria .
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2011, 15 (05) :424-431