Evidence map›Paper›PMID 33662572›Full record

ArticleNeuroImage2021

Dynamic analysis on simultaneous iEEG-MEG data via hidden Markov model.

Siqi Zhang, Chunyan Cao, Andrew Quinn, Umesh Vivekananda, Shikun Zhan, Wei Liu, Bomin Sun, Mark Woolrich, Qing Lu, Vladimir Litvak

Open access · goldAbstract read
In one paragraph

Article in NeuroImage, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  6. Canonical Hidden Markov Model Networks for studying M/EEG.Imaging neuroscience (Cambridge, Mass.)
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 2 countries.

Siqi ZhangKey Laboratory of Child Development and Learning Science of Ministry of Education, School of Biological Sciences & Medical Engineering, Southeast University, Nanjing 210096, Jiangsu, China; Wellcome Centre for Human Neuroimaging, UCL Institute of Neurology, 12 Queen Square, London WC1N 3BG, UK.
Chunyan CaoDepartment of Neurosurgery, affiliated Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Andrew QuinnOxford Centre for Human Brain Activity, University of Oxford, Warneford Hospital, Oxford, UK.
Umesh VivekanandaWellcome Centre for Human Neuroimaging, UCL Institute of Neurology, 12 Queen Square, London WC1N 3BG, UK; National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.
Shikun ZhanDepartment of Neurosurgery, affiliated Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Wei LiuDepartment of Neurosurgery, affiliated Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Bomin SunDepartment of Neurosurgery, affiliated Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Mark WoolrichOxford Centre for Human Brain Activity, University of Oxford, Warneford Hospital, Oxford, UK.
Qing LuKey Laboratory of Child Development and Learning Science of Ministry of Education, School of Biological Sciences & Medical Engineering, Southeast University, Nanjing 210096, Jiangsu, China. Electronic address: luq@seu.edu.cn.
Vladimir LitvakWellcome Centre for Human Neuroimaging, UCL Institute of Neurology, 12 Queen Square, London WC1N 3BG, UK. Electronic address: v.litvak@ucl.ac.uk.
Shanghai Jiao Tong University · CNWellcome Centre for Human Neuroimaging · GBWarneford Hospital · GBSoutheast University · CN

Funding

Medical Research Council MR/K005464/1Medical Research Council MR/L023784/2Medical Research Council MR/T033150/1Wellcome TrustWellcome Trust 203147/Z/16/Z
6 · The paper itself

Abstract

backgroundIntracranial electroencephalography (iEEG) recordings are used for clinical evaluation prior to surgical resection of the focus of epileptic seizures and also provide a window into normal brain function. A major difficulty with interpreting iEEG results at the group level is inconsistent placement of electrodes between subjects making it difficult to select contacts that correspond to the same functional areas. Recent work using time delay embedded hidden Markov model (HMM) applied to magnetoencephalography (MEG) resting data revealed a distinct set of brain states with each state engaging a specific set of cortical regions. Here we use a rare group dataset with simultaneously acquired resting iEEG and MEG to test whether there is correspondence between HMM states and iEEG power changes that would allow classifying iEEG contacts into functional clusters.

methodsSimultaneous MEG-iEEG recordings were performed at rest on 11 patients with epilepsy whose intracranial electrodes were implanted for pre-surgical evaluation. Pre-processed MEG sensor data was projected to source space. Time delay embedded HMM was then applied to MEG time series. At the same time, iEEG time series were analyzed with time-frequency decomposition to obtain spectral power changes with time. To relate MEG and iEEG results, correlations were computed between HMM probability time courses of state activation and iEEG power time course from the mid contact pair for each electrode in equally spaced frequency bins and presented as correlation spectra for the respective states and iEEG channels. Association of iEEG electrodes with HMM states based on significant correlations was compared to that based on the distance to peaks in subject-specific state topographies.

resultsFive HMM states were inferred from MEG. Two of them corresponded to the left and the right temporal activations and had a spectral signature primarily in the theta/alpha frequency band. All the electrodes had significant correlations with at least one of the states (p < 0.05 uncorrected) and for 27/50 electrodes these survived within-subject FDR correction (q < 0.05). These correlations peaked in the theta/alpha band. There was a highly significant dependence between the association of states and electrodes based on functional correlations and that based on spatial proximity (p = 5.6e

conclusionEpilepsy does not preclude HMM analysis of interictal data. The resulting group functional states are highly similar to those reported for healthy controls. Power changes recorded with iEEG correlate with HMM state time courses in the alpha-theta band and the presence of this correlation can be related to the spatial location of electrode contacts close to the individual peaks of the corresponding state topographies. Thus, the hypothesized relation between iEEG contacts and HMM states exists and HMM could be further explored as a method for identifying comparable iEEG channels across subjects for the purposes of group analysis.

Indexed as

Data AnalysisAdolescentAdultBrainElectrocorticographyEpilepsyFemaleHumansMagnetoencephalographyMaleMarkov ChainsMiddle AgedYoung AdultDynamicsHumanOscillationsResting state

Identifiers

PMID33662572
PMCPMC8204269
OpenAlexW3131520498

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.