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Quantifying brain connectivity signatures by means of polyconnectomic scoring

A broad range of neuropsychiatric disorders are associated with alterations in macroscale brain circuitry and connectivity. Identifying consistent brain patterns underlying these disorders by means of structural and functional MRI has proven challenging, partly due to the vast number of tests requir...

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Autores principales: Libedinsky, Ilan, Helwegen, Koen, Simón, Laura Guerrero, Gruber, Marius, Repple, Jonathan, Kircher, Tilo, Dannlowski, Udo, van den Heuvel, Martijn P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557693/
https://www.ncbi.nlm.nih.gov/pubmed/37808808
http://dx.doi.org/10.1101/2023.09.26.559327
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author Libedinsky, Ilan
Helwegen, Koen
Simón, Laura Guerrero
Gruber, Marius
Repple, Jonathan
Kircher, Tilo
Dannlowski, Udo
van den Heuvel, Martijn P.
author_facet Libedinsky, Ilan
Helwegen, Koen
Simón, Laura Guerrero
Gruber, Marius
Repple, Jonathan
Kircher, Tilo
Dannlowski, Udo
van den Heuvel, Martijn P.
author_sort Libedinsky, Ilan
collection PubMed
description A broad range of neuropsychiatric disorders are associated with alterations in macroscale brain circuitry and connectivity. Identifying consistent brain patterns underlying these disorders by means of structural and functional MRI has proven challenging, partly due to the vast number of tests required to examine the entire brain, which can lead to an increase in missed findings. In this study, we propose polyconnectomic score (PCS) as a metric designed to quantify the presence of disease-related brain connectivity signatures in connectomes. PCS summarizes evidence of brain patterns related to a phenotype across the entire landscape of brain connectivity into a subject-level score. We evaluated PCS across four brain disorders (autism spectrum disorder, schizophrenia, attention deficit hyperactivity disorder, and Alzheimer’s disease) and 14 studies encompassing ~35,000 individuals. Our findings consistently show that patients exhibit significantly higher PCS compared to controls, with effect sizes that go beyond other single MRI metrics ([min, max]: Cohen’s d = [0.30, 0.87], AUC = [0.58, 0.73]). We further demonstrate that PCS serves as a valuable tool for stratifying individuals, for example within the psychosis continuum, distinguishing patients with schizophrenia from their first-degree relatives (d = 0.42, p = 4 × 10(−3), FDR-corrected), and first-degree relatives from healthy controls (d = 0.34, p = 0.034, FDR-corrected). We also show that PCS is useful to uncover associations between brain connectivity patterns related to neuropsychiatric disorders and mental health, psychosocial factors, and body measurements.
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spelling pubmed-105576932023-10-07 Quantifying brain connectivity signatures by means of polyconnectomic scoring Libedinsky, Ilan Helwegen, Koen Simón, Laura Guerrero Gruber, Marius Repple, Jonathan Kircher, Tilo Dannlowski, Udo van den Heuvel, Martijn P. bioRxiv Article A broad range of neuropsychiatric disorders are associated with alterations in macroscale brain circuitry and connectivity. Identifying consistent brain patterns underlying these disorders by means of structural and functional MRI has proven challenging, partly due to the vast number of tests required to examine the entire brain, which can lead to an increase in missed findings. In this study, we propose polyconnectomic score (PCS) as a metric designed to quantify the presence of disease-related brain connectivity signatures in connectomes. PCS summarizes evidence of brain patterns related to a phenotype across the entire landscape of brain connectivity into a subject-level score. We evaluated PCS across four brain disorders (autism spectrum disorder, schizophrenia, attention deficit hyperactivity disorder, and Alzheimer’s disease) and 14 studies encompassing ~35,000 individuals. Our findings consistently show that patients exhibit significantly higher PCS compared to controls, with effect sizes that go beyond other single MRI metrics ([min, max]: Cohen’s d = [0.30, 0.87], AUC = [0.58, 0.73]). We further demonstrate that PCS serves as a valuable tool for stratifying individuals, for example within the psychosis continuum, distinguishing patients with schizophrenia from their first-degree relatives (d = 0.42, p = 4 × 10(−3), FDR-corrected), and first-degree relatives from healthy controls (d = 0.34, p = 0.034, FDR-corrected). We also show that PCS is useful to uncover associations between brain connectivity patterns related to neuropsychiatric disorders and mental health, psychosocial factors, and body measurements. Cold Spring Harbor Laboratory 2023-09-27 /pmc/articles/PMC10557693/ /pubmed/37808808 http://dx.doi.org/10.1101/2023.09.26.559327 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Libedinsky, Ilan
Helwegen, Koen
Simón, Laura Guerrero
Gruber, Marius
Repple, Jonathan
Kircher, Tilo
Dannlowski, Udo
van den Heuvel, Martijn P.
Quantifying brain connectivity signatures by means of polyconnectomic scoring
title Quantifying brain connectivity signatures by means of polyconnectomic scoring
title_full Quantifying brain connectivity signatures by means of polyconnectomic scoring
title_fullStr Quantifying brain connectivity signatures by means of polyconnectomic scoring
title_full_unstemmed Quantifying brain connectivity signatures by means of polyconnectomic scoring
title_short Quantifying brain connectivity signatures by means of polyconnectomic scoring
title_sort quantifying brain connectivity signatures by means of polyconnectomic scoring
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557693/
https://www.ncbi.nlm.nih.gov/pubmed/37808808
http://dx.doi.org/10.1101/2023.09.26.559327
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