Genetic testing in the epilepsies-Report of the ILAE Genetics Commission

被引:140
作者
Ottman, Ruth [1 ,2 ,3 ,4 ]
Hirose, Shinichi [5 ]
Jain, Satish [6 ]
Lerche, Holger [7 ,8 ]
Lopes-Cendes, Iscia [9 ]
Noebels, Jeffrey L. [10 ]
Serratosa, Jose [11 ]
Zara, Federico [12 ]
Scheffer, Ingrid E. [13 ,14 ]
机构
[1] Columbia Univ, Gertrude H Sergievsky Ctr, New York, NY 10027 USA
[2] Columbia Univ, Dept Epidemiol, New York, NY 10027 USA
[3] Columbia Univ, Dept Neurol, New York, NY 10027 USA
[4] New York State Psychiat Inst & Hosp, Div Epidemiol, New York, NY 10032 USA
[5] Fukuoka Univ, Dept Pediat, Fukuoka 81401, Japan
[6] Indian Epilepsy Ctr, New Delhi, India
[7] Univ Ulm, Neurol Klin, Ulm, Germany
[8] Univ Ulm, Inst Angew Physiol, Ulm, Germany
[9] Univ Estadual Campinas, UNICAMP, Campinas, SP, Brazil
[10] Baylor Coll Med, Dept Neurol, Houston, TX 77030 USA
[11] Univ Autonoma Madrid, Fdn Jimenez Diaz, Serv Neurol, Unidad Epilepsia, Madrid, Spain
[12] Inst G Gaslini, Dept Pediat, Neurogenet Lab, Genoa, Italy
[13] Univ Melbourne, Dept Med & Paediat, Melbourne, Vic, Australia
[14] Royal Childrens Hosp, Melbourne, Vic, Australia
关键词
Epilepsy; Seizures; Genetics; Genetic testing; SCN1A; IDIOPATHIC GENERALIZED EPILEPSY; SEVERE MYOCLONIC EPILEPSY; CHILDHOOD ABSENCE EPILEPSY; FRONTAL-LOBE EPILEPSY; POTASSIUM CHANNEL GENE; NEONATAL-INFANTILE SEIZURES; DOMINANT PARTIAL EPILEPSY; GLUCOSE-TRANSPORTER GLUT1; NEURONAL SODIUM-CHANNEL; EPISODIC ATAXIA TYPE-1;
D O I
10.1111/j.1528-1167.2009.02429.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
P>In this report, the International League Against Epilepsy (ILAE) Genetics Commission discusses essential issues to be considered with regard to clinical genetic testing in the epilepsies. Genetic research on the epilepsies has led to the identification of more than 20 genes with a major effect on susceptibility to idiopathic epilepsies. The most important potential clinical application of these discoveries is genetic testing: the use of genetic information, either to clarify the diagnosis in people already known or suspected to have epilepsy (diagnostic testing), or to predict onset of epilepsy in people at risk because of a family history (predictive testing). Although genetic testing has many potential benefits, it also has potential harms, and assessment of these potential benefits and harms in particular situations is complex. Moreover, many treating clinicians are unfamiliar with the types of tests available, how to access them, how to decide whether they should be offered, and what measures should be used to maximize benefit and minimize harm to their patients. Because the field is moving rapidly, with new information emerging practically every day, we present a framework for considering the clinical utility of genetic testing that can be applied to many different syndromes and clinical contexts. Given the current state of knowledge, genetic testing has high clinical utility in few clinical contexts, but in some of these it carries implications for daily clinical practice.
引用
收藏
页码:655 / 670
页数:16
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