Evidence map›Paper›PMID 34519351›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2022

Novel Gyrification Networks Reveal Links with Psychiatric Risk Factors in Early Illness.

Rachele Sanfelici, Anne Ruef, Linda A Antonucci, Nora Penzel, Aristeidis Sotiras, Mark Sen Dong, Maria Urquijo-Castro, Julian Wenzel, Lana Kambeitz-Ilankovic, Meike D Hettwer and 18 more

Abstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Trial
  2. Article
  3. Genetic insights on the mechanisms of human cortical folding.bioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
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

28 authors.

Rachele SanfeliciDepartment of Psychiatry and Psychotherapy, Ludwig-Maximilian University, Munich, 80336, Germany.ORCID 0000-0002-1674-9708
Anne RuefDepartment of Psychiatry and Psychotherapy, Ludwig-Maximilian University, Munich, 80336, Germany.
Linda A AntonucciDepartment of Psychiatry and Psychotherapy, Ludwig-Maximilian University, Munich, 80336, Germany.
Nora PenzelDepartment of Psychiatry and Psychotherapy, Faculty of Medicine and University Hospital, University of Cologne, Cologne, 50937, Germany.ORCID 0000-0003-1624-386X
Aristeidis SotirasDepartment of Radiology and Institute of Informatics, Washington University in St. Luis, st. Luis, MO63110, USA.
Mark Sen DongDepartment of Psychiatry and Psychotherapy, Ludwig-Maximilian University, Munich, 80336, Germany.
Maria Urquijo-CastroDepartment of Psychiatry and Psychotherapy, Ludwig-Maximilian University, Munich, 80336, Germany.
Julian WenzelDepartment of Psychiatry and Psychotherapy, Faculty of Medicine and University Hospital, University of Cologne, Cologne, 50937, Germany.
Lana Kambeitz-IlankovicDepartment of Psychiatry and Psychotherapy, Ludwig-Maximilian University, Munich, 80336, Germany.
Meike D HettwerMax Planck School of Cognition, Leipzig, 04103, Germany.
Stephan RuhrmannDepartment of Psychiatry and Psychotherapy, Faculty of Medicine and University Hospital, University of Cologne, Cologne, 50937, Germany.
Katharine ChisholmInstitute for Mental Health, University of Birmingham, Birmingham, B15 2TT, UK.
Anita Riecher-RösslerMedical Faculty, University of Basel, Basel, 4051, Switzerland.
Peter FalkaiDepartment of Psychiatry and Psychotherapy, Ludwig-Maximilian University, Munich, 80336, Germany.
Christos PantelisMelbourne Neuropsychiatry Centrem University of Melbourne & Melbourne Health, Melbourne, 3053, Australia.
Raimo K R SalokangasDepartment of Psychiatry, University of Turku, Turku, 20700, Finland.
Rebekka LencerDepartment of Psychiatry and Psychotherapy, University of Münster, Münster, 48149, Germany.
Alessandro BertolinoDepartment of Basic Medical Science, Neuroscience and Sense Organs, University of Bari Aldo Moro, Bari, 70124, Italy.
Joseph KambeitzDepartment of Psychiatry and Psychotherapy, Faculty of Medicine and University Hospital, University of Cologne, Cologne, 50937, Germany.
Eva MeisenzahlDepartment of Psychiatry and Psychotherapy, Medical Faculty, Heinrich-Heine University, Düsseldorf, 40629, Germany.
Stefan BorgwardtDepartment of Psychiatry and Psychotherapy, University of Lübeck, Lübeck, 23538, Germany.
Paolo BrambillaDepartment of Neurosciences and Mental Health, Fondazione IRCCS Ca' Grande Ospedale Maggiore Policlinico, Milano, 20122, Italy.ORCID 0000-0002-4021-8456
Stephen J WoodCentre for Youth Mental Health, University of Melbourne, Melbourne, 3052, Australia.
Rachel UpthegroveInstitute for Mental Health, University of Birmingham, Birmingham, B15 2TT, UK.
Frauke Schultze-LutterDepartment of Psychiatry and Psychotherapy, Medical Faculty, Heinrich-Heine University, Düsseldorf, 40629, Germany.
Nikolaos KoutsoulerisDepartment of Psychiatry and Psychotherapy, Ludwig-Maximilian University, Munich, 80336, Germany.
Dominic B DwyerDepartment of Psychiatry and Psychotherapy, Ludwig-Maximilian University, Munich, 80336, Germany.
PRONIA Consortium

Funding

Advanced machine learning algorithms that integrate multi-modal neuroimaging to quantify the heterogeneity in Alzheimer's DiseaseR01AG067103 · NIA · WASHINGTON UNIVERSITY · PI SOTIRAS, ARISTEIDIS · 2021 to 2025
$2.8M
NIA NIH HHS R01 AG067103
6 · The paper itself

Abstract

Adult gyrification provides a window into coordinated early neurodevelopment when disruptions predispose individuals to psychiatric illness. We hypothesized that the echoes of such disruptions should be observed within structural gyrification networks in early psychiatric illness that would demonstrate associations with developmentally relevant variables rather than specific psychiatric symptoms. We employed a new data-driven method (Orthogonal Projective Non-Negative Matrix Factorization) to delineate novel gyrification-based networks of structural covariance in 308 healthy controls. Gyrification within the networks was then compared to 713 patients with recent onset psychosis or depression, and at clinical high-risk. Associations with diagnosis, symptoms, cognition, and functioning were investigated using linear models. Results demonstrated 18 novel gyrification networks in controls as verified by internal and external validation. Gyrification was reduced in patients in temporal-insular, lateral occipital, and lateral fronto-parietal networks (pFDR < 0.01) and was not moderated by illness group. Higher gyrification was associated with better cognitive performance and lifetime role functioning, but not with symptoms. The findings demonstrated that gyrification can be parsed into novel brain networks that highlight generalized illness effects linked to developmental vulnerability. When combined, our study widens the window into the etiology of psychiatric risk and its expression in adulthood.

Indexed as

Magnetic Resonance ImagingPsychotic DisordersAdultBrainCerebral CortexHumansRisk Factorsclinical high riskcortical foldingdepressionpsychosisstructural covariance

Identifiers

PMID34519351
PMCPMC9016288

What OpenQuestion holds

Textmetadata
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.