Evidence map›Paper›PMID 30318906›Full record

ArticleBrain connectivity2019

Dynamic Functional Magnetic Resonance Imaging Connectivity Tensor Decomposition: A New Approach to Analyze and Interpret Dynamic Brain Connectivity.

Fatemeh Mokhtari, Paul J Laurienti, W Jack Rejeski, Grey Ballard

Abstract read
In one paragraph

Article in Brain connectivity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. A mixed-modeling framework for whole-brain dynamic network analysis.Network neuroscience (Cambridge, Mass.) · 2022
    Article
  7. Review
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

4 authors.

Fatemeh Mokhtari1 Laboratory for Complex Brain Networks, Department of Radiology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Paul J Laurienti1 Laboratory for Complex Brain Networks, Department of Radiology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
W Jack Rejeski1 Laboratory for Complex Brain Networks, Department of Radiology, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Grey Ballard5 Department of Computer Science, Wake Forest University, Winston-Salem, North Carolina.

Funding

Wake Forest Claude D. Pepper OAIC - RenewalP30AG021332 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Denise Kathryn Houston · 2002 to 2026
$36.4M
Wake Forest Clinical and Translational Science AwardUL1TR001420 · NCATS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ARD, JAMY D, FOLEY, KRISTIE L · 2015 to 2023
$32.3M
Cooperative Lifestyle Intervention Programs (CLIP-II)R18HL076441 · NHLBI · WAKE FOREST UNIVERSITY · PI MARSH, ANTHONY P, REJESKI, WALTER JOHN · 2012 to 2016
$3.1M
NCATS NIH HHS UL1 TR001420NHLBI NIH HHS R18 HL076441NIA NIH HHS P30 AG021332
6 · The paper itself

Abstract

There is a growing interest in using so-called dynamic functional connectivity, as the conventional static brain connectivity models are being questioned. Brain network analyses yield complex network data that are difficult to analyze and interpret. To deal with the complex structures, decomposition/factorization techniques that simplify the data are often used. For dynamic network analyses, data simplification is of even greater importance, as dynamic connectivity analyses result in a time series of complex networks. A new challenge that must be faced when using these decomposition/factorization techniques is how to interpret the resulting connectivity patterns. Connectivity patterns resulting from decomposition analyses are often visualized as networks in brain space, in the same way that pairwise correlation networks are visualized. This elevates the risk of conflating connections between nodes that represent correlations between nodes' time series with connections between nodes that result from decomposition analyses. Moreover, dynamic connectivity data may be represented with three-dimensional or four-dimensional (4D) tensors and decomposition results require unique interpretations. Thus, the primary goal of this article is to (1) address the issues that must be considered when interpreting the connectivity patterns from decomposition techniques and (2) show how the data structure and decomposition method interact to affect this interpretation. The outcome of our analyses is summarized as follows. (1) The edge strength in decomposition connectivity patterns represents complex relationships not pairwise interactions between the nodes. (2) The structure of the data significantly alters the connectivity patterns, for example, 4D data result in connectivity patterns with higher regional connections. (3) Orthogonal decomposition methods outperform in feature reduction applications, whereas nonorthogonal decomposition methods are better for mechanistic interpretation.

Indexed as

AgedBrainComputer SimulationConnectomeData Interpretation, StatisticalFemaleHumansImage Processing, Computer-AssistedMagnetic Resonance ImagingMaleNeural Pathwaysdynamic brain connectivityinterpretationtensor decomposition/factorization

Identifiers

PMID30318906
PMCPMC6390668

What OpenQuestion holds

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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.