Evidence map›Paper›PMID 34824347›Full record

ArticleScientific reports2021

Resting-state functional heterogeneity of the right insula contributes to pain sensitivity.

Dániel Veréb, Bálint Kincses, Tamás Spisák, Frederik Schlitt, Nikoletta Szabó, Péter Faragó, Krisztián Kocsis, Bence Bozsik, Eszter Tóth, András Király and 4 more

Open access · goldAbstract readMulticenter Study
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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 15% 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, 17 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

14 authors at 3 institutions in 2 countries.

Dániel VerébDepartment of Neurology, Faculty of Medicine, University of Szeged, Szeged, Hungary.
Bálint KincsesDepartment of Neurology, Faculty of Medicine, University of Szeged, Szeged, Hungary.
Tamás SpisákInstitute of Diagnostic and Interventional Radiology and Neuroradiology, University Hospital Essen, Essen, Germany.
Frederik SchlittDepartment of Neurology, University Hospital Essen, Essen, Germany.
Nikoletta SzabóDepartment of Neurology, Faculty of Medicine, University of Szeged, Szeged, Hungary.
Péter FaragóDepartment of Neurology, Faculty of Medicine, University of Szeged, Szeged, Hungary.
Krisztián KocsisDepartment of Neurology, Faculty of Medicine, University of Szeged, Szeged, Hungary.
Bence BozsikDepartment of Neurology, Faculty of Medicine, University of Szeged, Szeged, Hungary.
Eszter TóthDepartment of Neurology, Faculty of Medicine, University of Szeged, Szeged, Hungary.
András KirályDepartment of Neurology, Faculty of Medicine, University of Szeged, Szeged, Hungary.
Matthias ZunhammerDepartment of Neurology, University Hospital Essen, Essen, Germany.
Tobias Schmidt-WilckeInstitute of Clinical Neuroscience and Medical Psychology, University of Düsseldorf, Düsseldorf, Germany.
Ulrike BingelDepartment of Neurology, University Hospital Essen, Essen, Germany.
Zsigmond Tamás KincsesNeuroimaging Research Group, Department of Radiology, Albert Szent-Györgyi Clinical Center, University of Szeged, Semmelweis u. 6, Szeged, 6725, Hungary. kincses.zsigmond.tamas@med.u-szeged.hu.
University of Szeged · HUEssen University Hospital · DEHeinrich Heine University Düsseldorf · DE

Funding

Emberi Eroforrások Minisztériuma,Hungary 2017-1.2.1-NKP-2017-00002Emberi Eroforrások Minisztériuma,Hungary EFOP-3.6.1-16-2016-00008Emberi Eroforrások Minisztériuma,Hungary GINOP-2.3.2-15-2016-00034Emberi Eroforrások Minisztériuma,Hungary KTIA_13_NAP-A-II/20Emberi Eroforrások Minisztériuma,Hungary OTKA-FK-135870H2020 European Research Council H2020-MSCA-RISE-2016 734718National Research, Development and Innovation Office FK 135870National Research, Development and Innovation Office K 139415
6 · The paper itself

Abstract

Previous studies have described the structure and function of the insular cortex in terms of spatially continuous gradients. Here we assess how spatial features of insular resting state functional organization correspond to individual pain sensitivity. From a previous multicenter study, we included 107 healthy participants, who underwent resting state functional MRI scans, T1-weighted scans and quantitative sensory testing on the left forearm. Thermal and mechanical pain thresholds were determined. Connectopic mapping, a technique using non-linear representations of functional organization was employed to describe functional connectivity gradients in both insulae. Partial coefficients of determination were calculated between trend surface model parameters summarizing spatial features of gradients, modal and modality-independent pain sensitivity. The dominant connectopy captured the previously reported posteroanterior shift in connectivity profiles. Spatial features of dominant connectopies in the right insula explained significant amounts of variance in thermal (R

Indexed as

Brain MappingBrain WavesMagnetic Resonance ImagingPain ThresholdAdultConnectomeFemaleGermanyHumansHungaryInsular CortexMalePainPredictive Value of TestsRestYoung Adult

Identifiers

PMID34824347
PMCPMC8617295
OpenAlexW3215261658

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.