کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5631354 | 1580864 | 2017 | 14 صفحه PDF | دانلود رایگان |
- First study of single-trial correlations between the phase amplitude coupling strength and BOLD.
- Intracranial EEG and fMRI data simultaneously recorded in humans during a motor task.
- PACβγ strength explains variance of BOLD in addition a combination of α, β, and γ band powers.
Although it has been consistently found that local blood-oxygen-level-dependent (BOLD) changes are better modelled by a combination of the power of multiple EEG frequency bands rather than by the power of a unique band alone, the local electro-haemodynamic coupling function is not yet fully characterised. Electrophysiological studies have revealed that the strength of the coupling between the phase of low- and the amplitude of high- frequency EEG activities (phase-amplitude coupling - PAC) has an important role in brain function in general, and in preparation and execution of movement in particular. Using electrocorticographic (ECoG) and functional magnetic resonance imaging (fMRI) data recorded simultaneously in humans performing a finger-tapping task, we investigated the single-trial relationship between the amplitude of the BOLD signal and the strength of PAC and the power of α, β, and γ bands, at a local level. In line with previous studies, we found a positive correlation for the γ band, and negative correlations for the PACβγ strength, and the α and β bands. More importantly, we found that the PACβγ strength explained variance of the amplitude of the BOLD signal that was not explained by a combination of the α, β, and γ band powers. Our main finding sheds further light on the distinct nature of PAC as a functionally relevant mechanism and suggests that the sensitivity of EEG-informed fMRI studies may increase by including the PAC strength in the BOLD signal model, in addition to the power of the low- and high- frequency EEG bands.
Journal: NeuroImage - Volume 146, 1 February 2017, Pages 438-451