Evidence map›Paper›PMID 34732759›Full record

ArticleScientific reports2021

Abnormal nodal and global network organization in resting state functional MRI from subjects with the 22q11 deletion syndrome.

Teuntje A D Pelgrim, Matthijs G Bossong, Analía Cuiza, Luz María Alliende, Carlos Mena, Angeles Tepper, Juan Pablo Ramirez-Mahaluf, Barbara Iruretagoyena, Claudia Ornstein, Rosemarie Fritsch and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

14 authors at 5 institutions in 2 countries.

Teuntje A D PelgrimDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile.
Matthijs G BossongDepartment of Psychiatry, UMC Utrecht Brain Center, Utrecht University, Utrecht, The Netherlands.
Analía CuizaDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile.
Luz María AlliendeDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile.
Carlos MenaDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile.
Angeles TepperDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile.
Juan Pablo Ramirez-MahalufDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile.
Barbara IruretagoyenaDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile.
Claudia OrnsteinDepartamento de Psiquiatria y Salud Mental, Hospital Clinico Universidad de Chile, Santiago, Chile.
Rosemarie FritschDepartamento de Psiquiatria y Salud Mental, Hospital Clinico Universidad de Chile, Santiago, Chile.
Juan Pablo CruzDepartment of Radiology, Pontificia Universidad Católica de Chile, Santiago, Chile.
Cristian TejosDepartment of Electrical Engineering, Pontificia Universidad Católica de Chile, Santiago, Chile.
Gabriela RepettoGenetic and Genomic Center, Universidad del Desarrollo, Santiago, Chile.
Nicolas CrossleyDepartment of Psychiatry, Pontificia Universidad Católica de Chile, Santiago, Chile. ncrossley@uc.cl.
Pontificia Universidad Católica de Chile · CLHospital Clínico de la Universidad de Chile · CLUniversity Medical Center Utrecht · NLMillennium Science Initiative · CLUniversidad del Desarrollo · CL

Funding

Agencia Nacional de Investigación y Desarrollo (ANID) ANILLO PIA ACT192064
6 · The paper itself

Abstract

The 22q11 deletion syndrome is a genetic disorder associated with a high risk of developing psychosis, and is therefore considered a neurodevelopmental model for studying the pathogenesis of schizophrenia. Studies have shown that localized abnormal functional brain connectivity is present in 22q11 deletion syndrome like in schizophrenia. However, it is less clear whether these abnormal cortical interactions lead to global or regional network disorganization as seen in schizophrenia. We analyzed from a graph-theory perspective fMRI data from 40 22q11 deletion syndrome patients and 67 healthy controls, and reconstructed functional networks from 105 brain regions. Between-group differences were examined by evaluating edge-wise strength and graph theoretical metrics of local (weighted degree, nodal efficiency, nodal local efficiency) and global topological properties (modularity, local and global efficiency). Connectivity strength was globally reduced in patients, driven by a large network comprising 147 reduced connections. The 22q11 deletion syndrome network presented with abnormal local topological properties, with decreased local efficiency and reductions in weighted degree particularly in hub nodes. We found evidence for abnormal integration but intact segregation of the 22q11 deletion syndrome network. Results suggest that 22q11 deletion syndrome patients present with similar aberrant local network organization as seen in schizophrenia, and this network configuration might represent a vulnerability factor to psychosis.

Indexed as

22q11 Deletion SyndromeAdultCase-Control StudiesConnectomeFemaleHumansImage Processing, Computer-AssistedMagnetic Resonance ImagingMaleNerve NetNeural PathwaysRestYoung Adult

Identifiers

PMID34732759
PMCPMC8566599
OpenAlexW3208417213

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.