Evidence map›Paper›PMID 26417648›Full record

ArticleHuman brain mapping2015

Patient specific hemodynamic response functions associated with interictal discharges recorded via simultaneous intracranial EEG-fMRI.

Craig A Beers, Rebecca J Williams, Ismael Gaxiola-Valdez, Daniel J Pittman, Anita T Kang, Yahya Aghakhani, G Bruce Pike, Bradley G Goodyear, Paolo Federico

Open access · bronzeAbstract read
In one paragraph

Article in Human brain mapping, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

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  9. Identification of neurovascular changes associated with cerebral amyloid angiopathy from subject-specific hemodynamic response functions.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2017
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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

9 authors at 1 institution in 1 country.

Craig A BeersDepartment of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
Rebecca J WilliamsHotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.
Ismael Gaxiola-ValdezDepartment of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
Daniel J PittmanDepartment of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
Anita T KangHotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.
Yahya AghakhaniDepartment of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
G Bruce PikeDepartment of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
Bradley G GoodyearDepartment of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
Paolo FedericoDepartment of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.
University of Calgary · CA

Funding

Canadian Institutes of Health Research MOP-136839
6 · The paper itself

Abstract

Simultaneous collection of scalp EEG and fMRI has become an important tool for studying the hemodynamic changes associated with interictal epileptiform discharges (IEDs) in persons with epilepsy, and has become a standard presurgical assessment tool in some centres. We previously demonstrated that performing EEG-fMRI using intracranial electrodes (iEEG-fMRI) is of low risk to patients in our research centre, and offers unique insight into BOLD signal changes associated with IEDs recorded from very discrete sources. However, it is unknown whether the BOLD response corresponding to IEDs recorded by iEEG-fMRI follows the canonical hemodynamic response. We therefore scanned 11 presurgical epilepsy patients using iEEG-fMRI, and assessed the hemodynamic response associated with individual IEDs using two methods: assessment of BOLD signal changes associated with isolated IEDs at the location of the active intracranial electrode, and by estimating subject-specific impulse response functions to isolated IEDs. We found that the hemodynamic response associated with the intracranially recorded discharges varied by patient and by spike location. The observed shape and timing differences also deviated from the canonical hemodynamic response function traditionally used in many fMRI experiments. It is recommended that future iEEG-fMRI studies of IEDs use a flexible hemodynamic response model when performing parametric tests to accurately characterize these data.

Indexed as

AdultBrainBrain MappingBrain WavesElectroencephalographyEpilepsyFemaleHumansImage Processing, Computer-AssistedMagnetic Resonance ImagingMaleMiddle AgedOxygenTime FactorsYoung AdultOxygenBOLD responseepilepsyepileptiform dischargeseizure focus

Identifiers

PMID26417648
PMCPMC6869833
OpenAlexW2144707573

What OpenQuestion holds

Textmetadata
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.