Evidence map›Paper›PMID 37950937›Full record

ArticleMedical image analysis2024

Whole-brain multivariate hemodynamic deconvolution for functional MRI with stability selection.

Eneko Uruñuela, Javier Gonzalez-Castillo, Charles Zheng, Peter Bandettini, César Caballero-Gaudes

Open access · greenAbstract read
In one paragraph

Article in Medical image analysis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

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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

5 authors at 3 institutions in 2 countries.

Eneko UruñuelaBasque Center on Cognition, Brain and Language, Donostia - San Sebastián, Spain; University of the Basque Country (EHU/UPV), Donostia-San Sebastián, Spain. Electronic address: e.urunuela@bcbl.eu.
Javier Gonzalez-CastilloSection on Functional Imaging Methods, National Institute of Mental Health, Bethesda, MD 20892, United States.
Charles ZhengMachine Learning Team, Functional Magnetic Resonance Imaging Facility, National Institute of Mental Health, Bethesda, MD 20892, United States.
Peter BandettiniSection on Functional Imaging Methods, National Institute of Mental Health, Bethesda, MD 20892, United States.
César Caballero-GaudesBasque Center on Cognition, Brain and Language, Donostia - San Sebastián, Spain. Electronic address: c.caballero@bcbl.eu.
National Institute of Mental Health · USBasque Center on Cognition, Brain and Language · ESUniversity of the Basque Country · ES

Funding

Functional MRI Method DevelopmentZIAMH002783 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI BANDETTINI, PETER · 2009 to 2025
$38.4M
Intramural NIH HHS Z99 MH999999
6 · The paper itself

Abstract

Conventionally, analysis of functional MRI (fMRI) data relies on available information about the experimental paradigm to establish hypothesized models of brain activity. However, this information can be inaccurate, incomplete or unavailable in multiple scenarios such as resting-state, naturalistic paradigms or clinical conditions. In these cases, blind estimates of neuronal-related activity can be obtained with paradigm-free analysis methods such as hemodynamic deconvolution. Yet, current formulations of the hemodynamic deconvolution problem have three important limitations: (1) their efficacy strongly depends on the appropriate selection of regularization parameters, (2) being univariate, they do not take advantage of the information present across the brain, and (3) they do not provide any measure of statistical certainty associated with each detected event. Here we propose a novel approach that addresses all these limitations. Specifically, we introduce multivariate sparse paradigm free mapping (Mv-SPFM), a novel hemodynamic deconvolution algorithm that operates at the whole brain level and adds spatial information via a mixed-norm regularization term over all voxels. Additionally, Mv-SPFM employs a stability selection procedure that removes the need to select regularization parameters and also lets us obtain an estimate of the true probability of having a neuronal-related BOLD event at each voxel and time-point based on the area under the curve (AUC) of the stability paths. Besides, we present a formulation tailored for multi-echo fMRI acquisitions (MvME-SPFM), which allows us to better isolate fluctuations of BOLD origin on the basis of their linear dependence with the echo time (TE) and to assign physiologically interpretable units (i.e., changes in the apparent transverse relaxation ΔR

Indexed as

BrainBrain MappingAlgorithmsHemodynamicsHumansMagnetic Resonance ImagingHemodynamic deconvolutionInverse problemsMulti-echo fMRIStability selection

Identifiers

PMID37950937
PMCPMC10843584
OpenAlexW4388441728

What OpenQuestion holds

Textmetadata
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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.