Evidence map›Paper›PMID 26740914›Full record

ArticleNeuroImage. Clinical2015

Semi-metric analysis of the functional brain network: Relationship with familial risk for psychotic disorder.

Sanne Peeters, Tiago Simas, John Suckling, Ed Gronenschild, Ameera Patel, Petra Habets, Jim van Os, Machteld Marcelis, for Genetic Risk and Outcome of Psychosis (G.R.O.U.P.)

Open access · goldAbstract read
In one paragraph

Article in NeuroImage. Clinical, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 12 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

9 authors at 5 institutions in 2 countries.

Sanne PeetersDepartment of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, EURON, Maastricht University Medical Centre, PO Box 616 (Vijv1), 6200 MD Maastricht, The Netherlands; Faculty of Psychology and Educational Sciences, Open University of the Netherlands, Heerlen, The Netherlands.
Tiago SimasBehavioral and Clinical Neuroscience Institute, Department of Psychiatry, University of Cambridge, United Kingdom.
John SucklingBehavioral and Clinical Neuroscience Institute, Department of Psychiatry, University of Cambridge, United Kingdom; Cambridge and Peterborough Foundation NHS Trust. Cambridge, United Kingdom.
Ed GronenschildDepartment of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, EURON, Maastricht University Medical Centre, PO Box 616 (Vijv1), 6200 MD Maastricht, The Netherlands.
Ameera PatelBehavioral and Clinical Neuroscience Institute, Department of Psychiatry, University of Cambridge, United Kingdom.
Petra HabetsDepartment of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, EURON, Maastricht University Medical Centre, PO Box 616 (Vijv1), 6200 MD Maastricht, The Netherlands.
Jim van OsDepartment of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, EURON, Maastricht University Medical Centre, PO Box 616 (Vijv1), 6200 MD Maastricht, The Netherlands; King's College London, King's Health Partners, Department of Psychosis Studies Institute of Psychiatry, London, United Kingdom.
Machteld MarcelisDepartment of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, EURON, Maastricht University Medical Centre, PO Box 616 (Vijv1), 6200 MD Maastricht, The Netherlands; Institute for Mental Health Care Eindhoven (GGzE), Eindhoven, The Netherlands.
for Genetic Risk and Outcome of Psychosis (G.R.O.U.P.)
Maastricht University Medical Centre · NLUniversity of Cambridge · GBCambridgeshire and Peterborough NHS Foundation Trust · GBEuropean Graduate School of Neuroscience · NLKings Health Partners · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDysconnectivity in schizophrenia can be understood in terms of dysfunctional integration of a distributed network of brain regions. Here we propose a new methodology to analyze complex networks based on semi-metric behavior, whereby higher levels of semi-metricity may represent a higher level of redundancy and dispersed communication. It was hypothesized that individuals with (increased risk for) psychotic disorder would have more semi-metric paths compared to controls and that this would be associated with symptoms.

methodsResting-state functional MRI scans were obtained from 73 patients with psychotic disorder, 83 unaffected siblings and 72 controls. Semi-metric percentages (SMP) at the whole brain, hemispheric and lobar level were the dependent variables in a multilevel random regression analysis to investigate group differences. SMP was further examined in relation to symptomatology (i.e., psychotic/cognitive symptoms).

resultsAt the whole brain and hemispheric level, patients had a significantly higher SMP compared to siblings and controls, with no difference between the latter. In the combined sibling and control group, individuals with high schizotypy had intermediate SMP values in the left hemisphere with respect to patients and individuals with low schizotypy. Exploratory analyses in patients revealed higher SMP in 12 out of 42 lobar divisions compared to controls, of which some were associated with worse PANSS symptomatology (i.e., positive symptoms, excitement and emotional distress) and worse cognitive performance on attention and emotion processing tasks. In the combined group of patients and controls, working memory, attention and social cognition were associated with higher SMP. DISCUSSION: The results are suggestive of more dispersed network communication in patients with psychotic disorder, with some evidence for trait-based network alterations in high-schizotypy individuals. Dispersed communication may contribute to the clinical phenotype in psychotic disorder. In addition, higher SMP may contribute to neuro- and social cognition, independent of psychosis risk.

Indexed as

Genetic Predisposition to DiseaseAdultBrainBrain MappingData Interpretation, StatisticalFemaleHumansImage Processing, Computer-AssistedMagnetic Resonance ImagingMalePsychotic DisordersRisk FactorsSiblingsYoung AdultFunctional brain networkGraph theoryPsychotic disorderResting-state fMRISemi-metric percentageUnaffected siblings

Identifiers

PMID26740914
PMCPMC4644247
OpenAlexW1955079485

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.