Literature DB >> 27364472

Connectome sensitivity or specificity: which is more important?

Andrew Zalesky1, Alex Fornito2, Luca Cocchi3, Leonardo L Gollo3, Martijn P van den Heuvel4, Michael Breakspear5.   

Abstract

Connectomes with high sensitivity and high specificity are unattainable with current axonal fiber reconstruction methods, particularly at the macro-scale afforded by magnetic resonance imaging. Tensor-guided deterministic tractography yields sparse connectomes that are incomplete and contain false negatives (FNs), whereas probabilistic methods steered by crossing-fiber models yield dense connectomes, often with low specificity due to false positives (FPs). Densely reconstructed probabilistic connectomes are typically thresholded to improve specificity at the cost of a reduction in sensitivity. What is the optimal tradeoff between connectome sensitivity and specificity? We show empirically and theoretically that specificity is paramount. Our evaluations of the impact of FPs and FNs on empirical connectomes indicate that specificity is at least twice as important as sensitivity when estimating key properties of brain networks, including topological measures of network clustering, network efficiency and network modularity. Our asymptotic analysis of small-world networks with idealized modular structure reveals that as the number of nodes grows, specificity becomes exactly twice as important as sensitivity to the estimation of the clustering coefficient. For the estimation of network efficiency, the relative importance of specificity grows linearly with the number of nodes. The greater importance of specificity is due to FPs occurring more prevalently between network modules rather than within them. These spurious inter-modular connections have a dramatic impact on network topology. We argue that efforts to maximize the sensitivity of connectome reconstruction should be realigned with the need to map brain networks with high specificity.
Copyright © 2016 Elsevier Inc. All rights reserved.

Keywords:  Clustering coefficient; Complex networks; Connectome; False negatives; False positives; Modularity; Network efficiency; Sensitivity; Specificity; Tractography

Mesh:

Year:  2016        PMID: 27364472     DOI: 10.1016/j.neuroimage.2016.06.035

Source DB:  PubMed          Journal:  Neuroimage        ISSN: 1053-8119            Impact factor:   6.556


  93 in total

1.  Default mode network abnormalities in posttraumatic stress disorder: A novel network-restricted topology approach.

Authors:  Teddy J Akiki; Christopher L Averill; Kristen M Wrocklage; J Cobb Scott; Lynnette A Averill; Brian Schweinsburg; Aaron Alexander-Bloch; Brenda Martini; Steven M Southwick; John H Krystal; Chadi G Abdallah
Journal:  Neuroimage       Date:  2018-05-03       Impact factor: 6.556

2.  Charting shared developmental trajectories of cortical thickness and structural connectivity in childhood and adolescence.

Authors:  Gareth Ball; Richard Beare; Marc L Seal
Journal:  Hum Brain Mapp       Date:  2019-07-16       Impact factor: 5.038

3.  A comparison of diffusion tractography techniques in simulating the generalized Ising model to predict the intrinsic activity of the brain.

Authors:  Pubuditha M Abeyasinghe; Marco Aiello; Carlo Cavaliere; Adrian M Owen; Andrea Soddu
Journal:  Brain Struct Funct       Date:  2021-02-01       Impact factor: 3.270

4.  The open diffusion data derivatives, brain data upcycling via integrated publishing of derivatives and reproducible open cloud services.

Authors:  Paolo Avesani; Brent McPherson; Soichi Hayashi; Cesar F Caiafa; Robert Henschel; Eleftherios Garyfallidis; Lindsey Kitchell; Daniel Bullock; Andrew Patterson; Emanuele Olivetti; Olaf Sporns; Andrew J Saykin; Lei Wang; Ivo Dinov; David Hancock; Bradley Caron; Yiming Qian; Franco Pestilli
Journal:  Sci Data       Date:  2019-05-23       Impact factor: 6.444

5.  Geometric renormalization unravels self-similarity of the multiscale human connectome.

Authors:  Muhua Zheng; Antoine Allard; Patric Hagmann; Yasser Alemán-Gómez; M Ángeles Serrano
Journal:  Proc Natl Acad Sci U S A       Date:  2020-08-05       Impact factor: 11.205

6.  Continuous representations of brain connectivity using spatial point processes.

Authors:  Daniel Moyer; Boris A Gutman; Joshua Faskowitz; Neda Jahanshad; Paul M Thompson
Journal:  Med Image Anal       Date:  2017-04-28       Impact factor: 8.545

7.  Dynamic reorganization of the frontal parietal network during cognitive control and episodic memory.

Authors:  Kimberly L Ray; J Daniel Ragland; Angus W MacDonald; James M Gold; Steven M Silverstein; Deanna M Barch; Cameron S Carter
Journal:  Cogn Affect Behav Neurosci       Date:  2020-02       Impact factor: 3.282

8.  Tracking and validation techniques for topographically organized tractography.

Authors:  Dogu Baran Aydogan; Yonggang Shi
Journal:  Neuroimage       Date:  2018-07-02       Impact factor: 6.556

9.  White Matter Disruptions in Schizophrenia Are Spatially Widespread and Topologically Converge on Brain Network Hubs.

Authors:  Paul Klauser; Simon T Baker; Vanessa L Cropley; Chad Bousman; Alex Fornito; Luca Cocchi; Janice M Fullerton; Paul Rasser; Ulrich Schall; Frans Henskens; Patricia T Michie; Carmel Loughland; Stanley V Catts; Bryan Mowry; Thomas W Weickert; Cynthia Shannon Weickert; Vaughan Carr; Rhoshel Lenroot; Christos Pantelis; Andrew Zalesky
Journal:  Schizophr Bull       Date:  2017-03-01       Impact factor: 9.306

10.  Modular Segregation of Structural Brain Networks Supports the Development of Executive Function in Youth.

Authors:  Graham L Baum; Rastko Ciric; David R Roalf; Richard F Betzel; Tyler M Moore; Russell T Shinohara; Ari E Kahn; Simon N Vandekar; Petra E Rupert; Megan Quarmley; Philip A Cook; Mark A Elliott; Kosha Ruparel; Raquel E Gur; Ruben C Gur; Danielle S Bassett; Theodore D Satterthwaite
Journal:  Curr Biol       Date:  2017-05-25       Impact factor: 10.834

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.