Keyword search (3,447 papers available)


Detection of abnormal resting-state networks in individual patients suffering from focal epilepsy: an initial step toward individual connectivity assessment.

Author(s): Dansereau CL, Bellec P, Lee K, Pittau F, Gotman J, Grova C

Front Neurosci. 2014;8:419 Authors: Dansereau CL, Bellec P, Lee K, Pittau F, Gotman J, Grova C

Article GUID: 25565949

Detection and Magnetic Source Imaging of Fast Oscillations (40-160 Hz) Recorded with Magnetoencephalography in Focal Epilepsy Patients.

Author(s): von Ellenrieder N, Pellegrino G, Hedrich T, Gotman J, Lina JM, Grova C, Kobayashi E

Brain Topogr. 2016 Mar;29(2):218-31 Authors: von Ellenrieder N, Pellegrino G, Hedrich T, Gotman J, Lina JM, Grova C, Kobayashi E

Article GUID: 26830767

SPARK: Sparsity-based analysis of reliable k-hubness and overlapping network structure in brain functional connectivity.

Author(s): Lee K, Lina JM, Gotman J, Grova C

Neuroimage. 2016 07 01;134:434-449 Authors: Lee K, Lina JM, Gotman J, Grova C

Article GUID: 27046111

Disruption, emergence and lateralization of brain network hubs in mesial temporal lobe epilepsy.

Author(s): Lee K, Khoo HM, Lina JM, Dubeau F, Gotman J, Grova C

Neuroimage Clin. 2018;20:71-84 Authors: Lee K, Khoo HM, Lina JM, Dubeau F, Gotman J, Grova C

Article GUID: 30094158

Automatic classification and removal of structured physiological noise for resting state functional connectivity MRI analysis.

Author(s): Lee K, Khoo HM, Fourcade C, Gotman J, Grova C

Magn Reson Imaging. 2019 05;58:97-107 Authors: Lee K, Khoo HM, Fourcade C, Gotman J, Grova C

Article GUID: 30695721


Title:Automatic classification and removal of structured physiological noise for resting state functional connectivity MRI analysis.
Authors:Lee KKhoo HMFourcade CGotman JGrova C
Link:https://www.ncbi.nlm.nih.gov/pubmed/30695721?dopt=Abstract
DOI:10.1016/j.mri.2019.01.019
Category:Magn Reson Imaging
PMID:30695721
Dept Affiliation: PERFORM
1 Multimodal Functional Imaging Lab, Department of Biomedical Engineering, McGill University, Duff Medical Building, 3775 Rue University, Montreal, QC H3A 2B4, Canada; Montreal Neurological Institute, McGill University, 3801 Rue University, Montreal, QC H3A 2B4, Canada. Electronic address: kangjoo.lee@mail.mcgill.ca.
2 Montreal Neurological Institute, McGill University, 3801 Rue University, Montreal, QC H3A 2B4, Canada; Department of Neurosurgery, Osaka University, 2-2 Yamadaoka, Suita, Osaka Prefecture 565-0871, Japan.
3 Department of Physics and PERFORM Centre, Concordia University, 7200 Rue Sherbrooke St. W, Montreal, QC H4B 1R6, Canada.
4 Montreal Neurological Institute, McGill University, 3801 Rue University, Montreal, QC H3A 2B4, Canada.
5 Multimodal Functional Imaging Lab, Department of Biomedical Engineering, McGill University, Duff Medical Building, 3775 Rue University, Montreal, QC H3A 2B4, Canada; Montreal Neurological Institute, McGill University, 3801 Rue University, Montreal, QC H3A 2B4, Canada; Department of Physics and PERFORM Centre, Concordia University, 7200 Rue Sherbrooke St. W, Montreal, QC H4B 1R6, Canada.

Description:

Automatic classification and removal of structured physiological noise for resting state functional connectivity MRI analysis.

Magn Reson Imaging. 2019 05;58:97-107

Authors: Lee K, Khoo HM, Fourcade C, Gotman J, Grova C

Abstract

Resting state functional magnetic resonance imaging is used to study how brain regions are functionally connected by measuring temporal correlation of the fMRI signals, when a subject is at rest. Sparse dictionary learning is used to estimate a dictionary of resting state networks by decomposing the whole brain signals into several temporal features (atoms), each being shared by a set of voxels associated to a network. Recently, we proposed and validated a new method entitled Sparsity-based Analysis of Reliable K-hubness (SPARK), suggesting that connector hubs of brain networks participating in inter-network communication can be identified by counting the number of atoms involved in each voxel (sparse number k). However, such hub analysis can be corrupted by the presence of noise-related atoms, where physiological fluctuations in cardiorespiratory processes may remain even after band-pass filtering and regression of confound signals from the white matter and cerebrospinal fluid. Handling this issue might require manual classification of noisy atoms, which is a time-consuming and subjective task. Motivated by the fact that the physiological fluctuations are often localized in tissues close to large vasculatures, i.e. sagittal sinus, we propose an automatic classification of physiological noise-related atoms for SPARK using spatial priors and a stepwise regression procedure. We measured the degree to which the noise-characteristic time-courses within the mask are explained by each atom, and classified noise-related atoms using a subject-specific threshold estimated using a bootstrap resampling based strategy. Using real data from healthy subjects (N?=?25), manual classification of the atoms by two independent reviewers showed the presence of sagittal sinus related noise in 65% of the runs. Applying the same manual classification after the proposed automatic removal method reduced this rate to 19%. A 10-fold cross-validation on real data showed good specificity and accuracy of the proposed automated method in classifying the target noise (area under the ROC curve= 0.89), when compared to the manual classification considered as the reference. We demonstrated decrease in k-hubness values in the voxels involved in the sagittal sinus at both individual and group levels, suggesting a significant improvement of SPARK, which is particularly important when considering clinical applications.

PMID: 30695721 [PubMed - in process]