Evidence map›Paper›PMID 34971767›Full record

ArticleNeuroImage2022

A hierarchical Bayesian model to find brain-behaviour associations in incomplete data sets.

Fabio S Ferreira, Agoston Mihalik, Rick A Adams, John Ashburner, Janaina Mourao-Miranda

Abstract read
In one paragraph

Article in NeuroImage, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
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.

Fabio S FerreiraCentre for Medical Image Computing, Department of Computer Science, University College London, London, UK; Max Planck University College London Centre for Computational Psychiatry and Ageing Research, University College London, UK. Electronic address: fabio.ferreira.16@ucl.ac.uk.
Agoston MihalikCentre for Medical Image Computing, Department of Computer Science, University College London, London, UK; Max Planck University College London Centre for Computational Psychiatry and Ageing Research, University College London, UK.
Rick A AdamsCentre for Medical Image Computing, Department of Computer Science, University College London, London, UK; Max Planck University College London Centre for Computational Psychiatry and Ageing Research, University College London, UK; Wellcome Centre for Human Neuroimaging, University College London, London, UK.
John AshburnerWellcome Centre for Human Neuroimaging, University College London, London, UK.
Janaina Mourao-MirandaCentre for Medical Image Computing, Department of Computer Science, University College London, London, UK; Max Planck University College London Centre for Computational Psychiatry and Ageing Research, University College London, UK.

Funding

Mapping the Human Connectome: Structure, Function, and HeritabilityU54MH091657 · NIMH · WASHINGTON UNIVERSITY · PI UGURBIL, KAMIL, VAN ESSEN, DAVID C · 2010 to 2014
$34.7M
Medical Research Council MR/S007806/1NIMH NIH HHS U54 MH091657Wellcome Trust
6 · The paper itself

Abstract

Canonical Correlation Analysis (CCA) and its regularised versions have been widely used in the neuroimaging community to uncover multivariate associations between two data modalities (e.g., brain imaging and behaviour). However, these methods have inherent limitations: (1) statistical inferences about the associations are often not robust; (2) the associations within each data modality are not modelled; (3) missing values need to be imputed or removed. Group Factor Analysis (GFA) is a hierarchical model that addresses the first two limitations by providing Bayesian inference and modelling modality-specific associations. Here, we propose an extension of GFA that handles missing data, and highlight that GFA can be used as a predictive model. We applied GFA to synthetic and real data consisting of brain connectivity and non-imaging measures from the Human Connectome Project (HCP). In synthetic data, GFA uncovered the underlying shared and specific factors and predicted correctly the non-observed data modalities in complete and incomplete data sets. In the HCP data, we identified four relevant shared factors, capturing associations between mood, alcohol and drug use, cognition, demographics and psychopathological measures and the default mode, frontoparietal control, dorsal and ventral networks and insula, as well as two factors describing associations within brain connectivity. In addition, GFA predicted a set of non-imaging measures from brain connectivity. These findings were consistent in complete and incomplete data sets, and replicated previous findings in the literature. GFA is a promising tool that can be used to uncover associations between and within multiple data modalities in benchmark datasets (such as, HCP), and easily extended to more complex models to solve more challenging tasks.

Indexed as

BehaviorBrainDefault Mode NetworkMental ProcessesModels, TheoreticalNerve NetBayes TheoremConnectomeDatasets as TopicFactor Analysis, StatisticalHumansMagnetic Resonance ImagingBayesian inferenceBehaviourBrain connectivityGroup factor analysisMissing dataMultivariate methods

Identifiers

PMID34971767
PMCPMC8861855

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LicenceCC BY
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Registered trials

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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.