Biology subjects

Lina, J.-M.

Publications and source records attributed to Lina, J.-M..

4 recordsLinked to original sources

bioRxiv2021

Hemodynamic Correlates of Fluctuations in Neuronal Excitability: A Simultaneous Paired Associative Stimulation (PAS) and functional Near Infra-Red Spectroscopy (fNIRS) Study

BackgroundThe relationship between task-related hemodynamic activity and brain excitability is poorly understood in humans as it is technically challenging to combine simultaneously non-invasive brain stimulation and neuroimaging modalities. Cortical excitability corresponds to the readiness to become active and as such it may be linked to metabolic demand. HypothesesCortical excitability and hemodynamic activity are positively linked so that increases in hemodynamic activity correspond to increases in excitability and vice-versa. MethodsFluctuations of excitability and hemodynamic activity were investigated via simultaneous Transcranial Magnetic Stimulation (TMS) and functional Near Infrared Spectroscopy (fNIRS). Sixteen healthy subjects participated in a sham-controlled, pseudorandomized, counterbalanced study with PAS (PAS10/PAS25/Sham) on the right primary motor cortex (M1). The relationship between M1 excitability (Motor Evoked Potentials, MEP) and hemodynamic responses to finger tapping reconstructed via personalized fNIRS was assessed. ResultsHemodynamic activity exhibited a significant correlation with cortical excitability: increased HbO and HbR (absolute amplitude) corresponded to increased excitability and vice-versa (r=0.25; p=0.03 and r=0.16; p=0.17, respectively). The effect of PAS on excitability and hemodynamic activity showed a trend of positive correlation: correlation of MEP ratios (post-PAS/pre-PAS) with HbO and HbR ratios (r=0.19, p=0.29; r=0.18, p=0.30, respectively). ConclusionsTMS-fNIRS is a suitable technique for simultaneous investigation of excitability and hemodynamic responses and indicates a relationship between these two cortical properties. PAS effect is not limited to cortical excitability but also impacts hemodynamic processes. These findings have an impact on the application of neuromodulatory interventions in patients with neuropsychiatric disorders.

neuroscience↗

bioRxiv2021

Diffuse optical reconstructions of NIRS data using Maximum Entropy on the Mean

Functional near-infrared spectroscopy (fNIRS) measures the hemoglobin concentration changes associated with neuronal activity. Diffuse optical tomography (DOT) consists of reconstructing the optical density changes measured from scalp channels to the oxy-/deoxy-hemoglobin (i.e., HbO/HbR) concentration changes within the cortical regions. In the present study, we adapted a nonlinear source localization method developed and validated in the context of Electro- and Magneto-Encephalography (EEG/MEG): the Maximum Entropy on the Mean (MEM), to solve the inverse problem of DOT reconstruction. We first introduced depth weighting strategy within the MEM framework for DOT reconstruction to avoid biasing the reconstruction results of DOT towards superficial regions. We also proposed a new initialization of the MEM model improving the temporal accuracy of the original MEM framework. To evaluate MEM performance and compare with widely used depth weighted Minimum Norm Estimate (MNE) inverse solution, we applied a realistic simulation scheme which contained 4000 simulations generated by 250 different seeds at different locations and 4 spatial extents ranging from 3 to 40cm2 along the cortical surface. Our results showed that overall MEM provided more accurate DOT reconstructions than MNE. Moreover, we found that MEM was remained particularly robust in low signal-to-noise ratio (SNR) conditions. The proposed method was further illustrated by comparing to functional Magnetic Resonance Imaging (fMRI) activation maps, on real data involving finger tapping tasks with two different montages. The results showed that MEM provided more accurate HbO and HbR reconstructions in spatial agreement with the main fMRI cluster, when compared to MNE. HighlightsO_LIWe introduced a new fNIRS reconstruction method - Maximum Entropy on the Mean. C_LIO_LIWe implemented depth weighting strategy within the MEM framework. C_LIO_LIWe improved the temporal accuracy of the original MEM reconstruction. C_LIO_LIPerformances of MEM and MNE were evaluated with realistic simulations and real data. C_LIO_LIMEM provided more accurate and robust reconstructions than MNE. C_LI

neuroscience↗

bioRxiv2021

Sleeping at the Switch

Sleep slow waves are studied for their role in brain plasticity, homeostatic regulation and their changes during aging. Here, we address the possibility that two types of slow waves co-exist in humans. Thirty young and 29 older adults underwent a night of polysomnographic recordings. Using the Transition frequency, slow waves with a slow transition (slow switchers) and with a fast transition (fast switchers) were discovered. Slow switchers had a high EEG connectivity along their depolarization transition while fast switchers had a lower connectivity dynamic and dissipated faster during the night. Aging was associated with lower temporal dissipation of sleep pressure in slow and fast switchers and lower EEG connectivity at the microscale of the oscillations, suggesting a decreased flexibility in the connectivity network of older individuals. Our findings show that two different types of slow waves with possible distinct underlying functions, coexist in the slow wave spectrum.

neuroscience↗

bioRxiv2020

Data-driven beamforming techniques to attenuate ballistocardiogram (BCG) artefacts in EEG-fMRI without detecting cardiac pulses in electrocardiography (ECG) recordings

Simultaneous recording of EEG and fMRI is a very promising non-invasive neuroimaging technique, providing a wide range of complementary information to characterize underlying mechanisms associated with brain functions. However, EEG data obtained from the simultaneous EEG-fMRI recordings are strongly influenced by MRI related artefacts, namely gradient artefacts (GA) and ballistocardiogram (BCG) artefacts. The GA is induced by temporally varying magnetic field gradients used for MR imaging, whereas the BCG artefacts are produced by cardiac pulse driven head motion in the strong magnetic field of the MRI scanner, so that this BCG artefact will be present when the subject is lying in the scanner, even when no fMRI data are acquired. When compared to corrections of the GA, the BCG artefact corrections are more challenging to remove due to its inherent variabilities and dynamic changes over time. Typically, the BCG artefacts obscure the EEG signals below 20Hz, and this remains problematic especially when the frequency of interest of EEG signals is below 20Hz, such as Alpha (8-13Hz) and Beta (13-30Hz) band EEG activity, or sleep spindle (11-16Hz) and slow-wave oscillations (<1 Hz) during sleep. The standard BCG artefact corrections, as for instance Average Artefact Subtraction method (AAS), require detecting cardiac pulse (R-peak) events from simultaneous electrocardiography (ECG) recordings. However, ECG signals in the MRI scanner are sometimes distorted and will become problematic for detecting reliable R-peaks. In this study, we focused on a beamforming technique, which is a spatial filtering technique to reject sources of signal variance that do not appear dipolar in the source space. This technique attenuates all unwanted source activities outside of a presumed region of interest without having to specify the location or the configuration of these underlying source signals. Specifically, in this study, we revisited the advantages of the beamforming technique to attenuate the BCG artefact in EEG-fMRI, and also to recover meaningful task-based induced neural signals during an attentional network task (ANT) which required participants to identify visual cues and respond as accurately and quickly as possible. We analysed EEG-fMRI data in 20 healthy participants when they were performing the ANT, and compared four different BCG correction approaches (non-BCG corrected, AAS BCG corrected, beamforming+AAS BCG corrected, beamforming BCG corrected). We demonstrated that beamforming BCG corrected data did not only significantly reduce the BCG artefacts, but also significantly recovered the expected task-based induced brain activity when compared to the standard AAS BCG corrections. Without detecting R-peak events from the ECG, this data-driven beamforming technique appears promising especially for longer data acquisition of sleep and resting EEG-fMRI. Our findings extend previous work regarding the recovery of meaningful EEG signals by an optimized suppression of MRI related artefacts. HighlightsO_LIBeamforming spatial filtering technique attenuates ballistocardiogram (BCG) artefacts in EEG-fMRI without detecting cardiac pulses in electrocardiography (ECG) recordings. C_LIO_LIBeamforming BCG denoising technique recovers expected task-based induced visual alpha and motor beta event-related desynchronization (ERD). C_LIO_LIBeamforming technique improves signal-noise ratios (SNR) of neural activities as compared to sensor level signals. C_LIO_LIData-driven beamforming technique appears promising for longer data acquisition of sleep and resting EEG-fMRI without relying on ECG signals. C_LI

neuroscience↗