Evidence map›Paper›PMID 26308854›Full record

ArticlePloS one2015

Semi-Metric Topology of the Human Connectome: Sensitivity and Specificity to Autism and Major Depressive Disorder.

Tiago Simas, Shayanti Chattopadhyay, Cindy Hagan, Prantik Kundu, Ameera Patel, Rosemary Holt, Dorothea Floris, Julia Graham, Cinly Ooi, Roger Tait and 6 more

Abstract readComparative Study
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. The distance backbone of complex networks.Journal of complex networks · 2021
    Article
  4. Article
  5. Article
  6. Article
  7. Communication dynamics in complex brain networks.Nature reviews. Neuroscience · 2017
    Review
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Tiago SimasDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom.
Shayanti ChattopadhyayDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom.
Cindy HaganDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom; Department of Psychology, Columbia University, New York, New York, United States of America.
Prantik KunduDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom; Department of Radiology, Icahn School of Medicine at Mount Sinai, New York, New York, United States of America.
Ameera PatelDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom.
Rosemary HoltDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom.
Dorothea FlorisDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom.
Julia GrahamDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom; Department of Psychiatry, University of Oxford, Medical Sciences Division, Oxford, United Kingdom.
Cinly OoiDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom.
Roger TaitMRC/Wellcome Trust Behavioural and Clinical Neuroscience Institute, University of Cambridge, Cambridge, United Kingdom.
Michael SpencerDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom.
Simon Baron-CohenDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom; MRC/Wellcome Trust Behavioural and Clinical Neuroscience Institute, University of Cambridge, Cambridge, United Kingdom.
Barbara SahakianDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom; MRC/Wellcome Trust Behavioural and Clinical Neuroscience Institute, University of Cambridge, Cambridge, United Kingdom.
Ed BullmoreDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom; Cambridge and Peterborough Foundation NHS Trust, Cambridge, United Kingdom; MRC/Wellcome Trust Behavioural and Clinical Neuroscience Institute, University of Cambridge, Cambridge, United Kingdom.
Ian GoodyerDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom; Cambridge and Peterborough Foundation NHS Trust, Cambridge, United Kingdom; MRC/Wellcome Trust Behavioural and Clinical Neuroscience Institute, University of Cambridge, Cambridge, United Kingdom.
John SucklingDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom; Cambridge and Peterborough Foundation NHS Trust, Cambridge, United Kingdom; MRC/Wellcome Trust Behavioural and Clinical Neuroscience Institute, University of Cambridge, Cambridge, United Kingdom.

Funding

Department of Health 06/05/01Department of Health 97/29/01Medical Research Council G0001354Medical Research Council G0701919Medical Research Council G0802226Medical Research Council G1000183Wellcome Trust 093875
6 · The paper itself

Abstract

introductionThe human functional connectome is a graphical representation, consisting of nodes connected by edges, of the inter-relationships of blood oxygenation-level dependent (BOLD) time-series measured by MRI from regions encompassing the cerebral cortices and, often, the cerebellum. Semi-metric analysis of the weighted, undirected connectome distinguishes an edge as either direct (metric), such that there is no alternative path that is accumulatively stronger, or indirect (semi-metric), where one or more alternative paths exist that have greater strength than the direct edge. The sensitivity and specificity of this method of analysis is illustrated by two case-control analyses with independent, matched groups of adolescents with autism spectrum conditions (ASC) and major depressive disorder (MDD).

resultsSignificance differences in the global percentage of semi-metric edges was observed in both groups, with increases in ASC and decreases in MDD relative to controls. Furthermore, MDD was associated with regional differences in left frontal and temporal lobes, the right limbic system and cerebellum. In contrast, ASC had a broadly increased percentage of semi-metric edges with a more generalised distribution of effects and some areas of reduction. In summary, MDD was characterised by localised, large reductions in the percentage of semi-metric edges, whilst ASC is characterised by more generalised, subtle increases. These differences were corroborated in greater detail by inspection of the semi-metric backbone for each group; that is, the sub-graph of semi-metric edges present in >90% of participants, and by nodal degree differences in the semi-metric connectome.

conclusionThese encouraging results, in what we believe is the first application of semi-metric analysis to neuroimaging data, raise confidence in the methodology as potentially capable of detection and characterisation of a range of neurodevelopmental and psychiatric disorders.

Indexed as

AdolescentAutistic DisorderBrainCase-Control StudiesCerebellumCerebral CortexChildConnectomeFemaleHumansMagnetic Resonance ImagingMajor Depressive DisorderMaleNeuroimagingSensitivity and SpecificityTemporal Lobe

Identifiers

PMID26308854
PMCPMC4550361

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.