TY - JOUR
T1 - Estimating sensor-space EEG connectivity
T2 - Identifying best performing methods for functional connectivity in simulated data
AU - Miljevic, Aleksandra
AU - Murphy, Oscar W.
AU - Fitzgerald, Paul B.
AU - Bailey, Neil W.
N1 - Publisher Copyright:
© 2025 The Author(s)
PY - 2025/6
Y1 - 2025/6
N2 - Objective: Functional brain connectivity (FC) can be estimated using electroencephalography (EEG). However, there is considerable variability across studies in the FC measures used and in data (pre-)processing methods, leading to difficulties comparing and amalgamating results between studies. Thus, standardisation of EEG (pre-)processing for the measurement and reporting of FC is needed. We aimed to assess differences in FC estimates produced by different settings across multiple EEG pre-processing steps, (including re-referencing and epoching) to validate a reliable methodological pipeline for assessing EEG-FC in simulated EEG data. Methods: We simulated EEG-FC data where the ‘ground truth’ of the connections is known and compared estimates of FC from this ground truth data across multiple FC measures and variations in multiple pre-processing steps. Results: Our results indicated that pre-processing steps that included segmenting the data into 40 or more epochs that were 6 s or more in length provided the most accurate estimation of the simulated FC. With regards to the data re-referencing, the Reference Electrode Standardization Technique or the common average re-referencing appeared best when used in conjunction with imaginary coherence and weighted phase lag index metrics. However, the magnitude-squared coherence FC measure performed best with the Current Source Density reference free techniques. Conclusions & Significance: Our paper provides an evidence-base for the influence of referencing, epoch length and number, controls for volume conduction, and different FC metrics on EEG-FC measurement. Using this evidence, we present an initial and promising account of the best performing (pre-)processing choices for robust EEG-FC assessment.
AB - Objective: Functional brain connectivity (FC) can be estimated using electroencephalography (EEG). However, there is considerable variability across studies in the FC measures used and in data (pre-)processing methods, leading to difficulties comparing and amalgamating results between studies. Thus, standardisation of EEG (pre-)processing for the measurement and reporting of FC is needed. We aimed to assess differences in FC estimates produced by different settings across multiple EEG pre-processing steps, (including re-referencing and epoching) to validate a reliable methodological pipeline for assessing EEG-FC in simulated EEG data. Methods: We simulated EEG-FC data where the ‘ground truth’ of the connections is known and compared estimates of FC from this ground truth data across multiple FC measures and variations in multiple pre-processing steps. Results: Our results indicated that pre-processing steps that included segmenting the data into 40 or more epochs that were 6 s or more in length provided the most accurate estimation of the simulated FC. With regards to the data re-referencing, the Reference Electrode Standardization Technique or the common average re-referencing appeared best when used in conjunction with imaginary coherence and weighted phase lag index metrics. However, the magnitude-squared coherence FC measure performed best with the Current Source Density reference free techniques. Conclusions & Significance: Our paper provides an evidence-base for the influence of referencing, epoch length and number, controls for volume conduction, and different FC metrics on EEG-FC measurement. Using this evidence, we present an initial and promising account of the best performing (pre-)processing choices for robust EEG-FC assessment.
UR - https://www.scopus.com/pages/publications/105002238355
U2 - 10.1016/j.clinph.2025.03.043
DO - 10.1016/j.clinph.2025.03.043
M3 - Article
C2 - 40222212
AN - SCOPUS:105002238355
SN - 1388-2457
VL - 174
SP - 73
EP - 83
JO - Clinical Neurophysiology
JF - Clinical Neurophysiology
ER -