TY - JOUR
T1 - Using interictal seizure-free EEG data to recognise patients with epilepsy based on machine learning of brain functional connectivity
AU - Cao, J.
AU - Grajcar, K.
AU - Shan, X.
AU - Zhao, Y.
AU - Zou, J.
AU - Chen, L.
AU - Li, Z.
AU - Grunewald, R.
AU - Zis, P.
AU - De Marco, M.
AU - Unwin, Z.
AU - Blackburn, D.
AU - Sarrigiannis, P.G.
PY - 2021/5
Y1 - 2021/5
N2 - Most seizures in adults with epilepsy occur rather infrequently and as a result, the interictal EEG plays a crucial role in the diagnosis and classification of epilepsy. However, empirical interpretation, of a first EEG in adult patients, has a very low sensitivity ranging between 29–55 %. Useful EEG information remains buried within the signals in seizure-free EEG epochs, far beyond the observational capabilities of any specialised physician in this field. Unlike most of the existing works focusing on either seizure data or single-variate method, we introduce a multi-variate method to characterise sensor level brain functional connectivity from interictal EEG data to identify patients with generalised epilepsy. A total of 9 connectivity features based on 5 different measures in time, frequency and time-frequency domains have been tested. The solution has been validated by the K-Nearest Neighbour algorithm, classifying an epilepsy group (EG) vs healthy controls (HC) and subsequently with another cohort of patients characterised by non-epileptic attacks (NEAD), a psychogenic type of disorder. A high classification accuracy (97 %) was achieved for EG vs HC while revealing significant spatio-temporal deficits in the frontocentral areas in the beta frequency band. For EG vs NEAD, the classification accuracy was only about 73 %, which might be a reflection of the well-described coexistence of NEAD with epileptic attacks. Our work demonstrates that seizure-free interictal EEG data can be used to accurately classify patients with generalised epilepsy from HC and that more systematic work is required in this direction aiming to produce a clinically useful diagnostic method.
AB - Most seizures in adults with epilepsy occur rather infrequently and as a result, the interictal EEG plays a crucial role in the diagnosis and classification of epilepsy. However, empirical interpretation, of a first EEG in adult patients, has a very low sensitivity ranging between 29–55 %. Useful EEG information remains buried within the signals in seizure-free EEG epochs, far beyond the observational capabilities of any specialised physician in this field. Unlike most of the existing works focusing on either seizure data or single-variate method, we introduce a multi-variate method to characterise sensor level brain functional connectivity from interictal EEG data to identify patients with generalised epilepsy. A total of 9 connectivity features based on 5 different measures in time, frequency and time-frequency domains have been tested. The solution has been validated by the K-Nearest Neighbour algorithm, classifying an epilepsy group (EG) vs healthy controls (HC) and subsequently with another cohort of patients characterised by non-epileptic attacks (NEAD), a psychogenic type of disorder. A high classification accuracy (97 %) was achieved for EG vs HC while revealing significant spatio-temporal deficits in the frontocentral areas in the beta frequency band. For EG vs NEAD, the classification accuracy was only about 73 %, which might be a reflection of the well-described coexistence of NEAD with epileptic attacks. Our work demonstrates that seizure-free interictal EEG data can be used to accurately classify patients with generalised epilepsy from HC and that more systematic work is required in this direction aiming to produce a clinically useful diagnostic method.
KW - qEEG
KW - Classification
KW - Brain connectivity
KW - Correlation
KW - Coherence
UR - http://www.scopus.com/inward/record.url?eid=2-s2.0-85102269332&partnerID=MN8TOARS
U2 - 10.1016/j.bspc.2021.102554
DO - 10.1016/j.bspc.2021.102554
M3 - Article
SN - 1746-8094
VL - 67
JO - Biomedical Signal Processing and Control
JF - Biomedical Signal Processing and Control
M1 - 102554
ER -