TY - JOUR
T1 - Advances in the development of biomarkers for epilepsy
AU - Pitkänen, Asla
AU - Löscher, Wolfgang
AU - Vezzani, Annamaria
AU - Becker, Albert J.
AU - Simonato, Michele
AU - Lukasiuk, Katarzyna
AU - Gröhn, Olli
AU - Bankstahl, Jens P.
AU - Friedman, Alon
AU - Aronica, Eleonora
AU - Gorter, Jan A.
AU - Ravizza, Teresa
AU - Sisodiya, Sanjay M.
AU - Kokaia, Merab
AU - Beck, Heinz
N1 - Funding Information:
The authors are primarily supported by the FP7-HEALTH project 602102 (EPITARGET, all authors); the Academy of Finland (AP); Polish Ministry of Science and Education grant W19/7.PR/2014 (KL); Fondazione Monzino and Citizens United for Research in Epilepsy (AV and TR); the Niedersachsen-Research Network on Neuroinfectiology of the Ministry of Science and Culture of Lower Saxony, Germany (WL); the Israel Science Foundation (AF); FP7-PEOPLE-2011-IAPP project 285827 (EPIXCHANGE, MS and MK); and SFB1089 of the Deutsche Forschungsgemeinschaft (AJB and HB).
Funding Information:
SMS has received grants from UCB. HB has received personal fees from BIAL and UCB. All other authors declare no competing interests.
Publisher Copyright:
© 2016 Elsevier Ltd.
PY - 2016/7/1
Y1 - 2016/7/1
N2 - Over 50 million people worldwide have epilepsy. In nearly 30% of these cases, epilepsy remains unsatisfactorily controlled despite the availability of over 20 antiepileptic drugs. Moreover, no treatments exist to prevent the development of epilepsy in those at risk, despite an increasing understanding of the underlying molecular and cellular pathways. One of the major factors that have impeded rapid progress in these areas is the complex and multifactorial nature of epilepsy, and its heterogeneity. Therefore, the vision of developing targeted treatments for epilepsy relies upon the development of biomarkers that allow individually tailored treatment. Biomarkers for epilepsy typically fall into two broad categories: diagnostic biomarkers, which provide information on the clinical status of, and potentially the sensitivity to, specific treatments, and prognostic biomarkers, which allow prediction of future clinical features, such as the speed of progression, severity of epilepsy, development of comorbidities, or prediction of remission or cure. Prognostic biomarkers are of particular importance because they could be used to identify which patients will develop epilepsy and which might benefit from preventive treatments. Biomarker research faces several challenges; however, biomarkers could substantially improve the management of people with epilepsy and could lead to prevention in the right person at the right time, rather than just symptomatic treatment.
AB - Over 50 million people worldwide have epilepsy. In nearly 30% of these cases, epilepsy remains unsatisfactorily controlled despite the availability of over 20 antiepileptic drugs. Moreover, no treatments exist to prevent the development of epilepsy in those at risk, despite an increasing understanding of the underlying molecular and cellular pathways. One of the major factors that have impeded rapid progress in these areas is the complex and multifactorial nature of epilepsy, and its heterogeneity. Therefore, the vision of developing targeted treatments for epilepsy relies upon the development of biomarkers that allow individually tailored treatment. Biomarkers for epilepsy typically fall into two broad categories: diagnostic biomarkers, which provide information on the clinical status of, and potentially the sensitivity to, specific treatments, and prognostic biomarkers, which allow prediction of future clinical features, such as the speed of progression, severity of epilepsy, development of comorbidities, or prediction of remission or cure. Prognostic biomarkers are of particular importance because they could be used to identify which patients will develop epilepsy and which might benefit from preventive treatments. Biomarker research faces several challenges; however, biomarkers could substantially improve the management of people with epilepsy and could lead to prevention in the right person at the right time, rather than just symptomatic treatment.
UR - http://www.scopus.com/inward/record.url?scp=84973334395&partnerID=8YFLogxK
U2 - 10.1016/S1474-4422(16)00112-5
DO - 10.1016/S1474-4422(16)00112-5
M3 - Review article
AN - SCOPUS:84973334395
SN - 1474-4422
VL - 15
SP - 843
EP - 856
JO - The Lancet Neurology
JF - The Lancet Neurology
IS - 8
ER -