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Functional connectome fingerprinting across the lifespan

Systematic changes have been observed in the functional architecture of the human brain with advancing age. However, functional connectivity (FC) is also a powerful feature to detect unique “connectome fingerprints,” allowing identification of individuals among their peers. Although fingerprinting h...

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Autores principales: St-Onge, Frédéric, Javanray, Mohammadali, Pichet Binette, Alexa, Strikwerda-Brown, Cherie, Remz, Jordana, Spreng, R. Nathan, Shafiei, Golia, Misic, Bratislav, Vachon-Presseau, Étienne, Villeneuve, Sylvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MIT Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473304/
https://www.ncbi.nlm.nih.gov/pubmed/37781144
http://dx.doi.org/10.1162/netn_a_00320
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author St-Onge, Frédéric
Javanray, Mohammadali
Pichet Binette, Alexa
Strikwerda-Brown, Cherie
Remz, Jordana
Spreng, R. Nathan
Shafiei, Golia
Misic, Bratislav
Vachon-Presseau, Étienne
Villeneuve, Sylvia
author_facet St-Onge, Frédéric
Javanray, Mohammadali
Pichet Binette, Alexa
Strikwerda-Brown, Cherie
Remz, Jordana
Spreng, R. Nathan
Shafiei, Golia
Misic, Bratislav
Vachon-Presseau, Étienne
Villeneuve, Sylvia
author_sort St-Onge, Frédéric
collection PubMed
description Systematic changes have been observed in the functional architecture of the human brain with advancing age. However, functional connectivity (FC) is also a powerful feature to detect unique “connectome fingerprints,” allowing identification of individuals among their peers. Although fingerprinting has been robustly observed in samples of young adults, the reliability of this approach has not been demonstrated across the lifespan. We applied the fingerprinting framework to the Cambridge Centre for Ageing and Neuroscience cohort (n = 483 aged 18 to 89 years). We found that individuals are “fingerprintable” (i.e., identifiable) across independent functional MRI scans throughout the lifespan. We observed a U-shape distribution in the strength of “self-identifiability” (within-individual correlation across modalities), and “others-identifiability” (between-individual correlation across modalities), with a decrease from early adulthood into middle age, before improving in older age. FC edges contributing to self-identifiability were not restricted to specific brain networks and were different between individuals across the lifespan sample. Self-identifiability was additionally associated with regional brain volume. These findings indicate that individual participant-level identification is preserved across the lifespan despite the fact that its components are changing nonlinearly.
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spelling pubmed-104733042023-10-01 Functional connectome fingerprinting across the lifespan St-Onge, Frédéric Javanray, Mohammadali Pichet Binette, Alexa Strikwerda-Brown, Cherie Remz, Jordana Spreng, R. Nathan Shafiei, Golia Misic, Bratislav Vachon-Presseau, Étienne Villeneuve, Sylvia Netw Neurosci Research Article Systematic changes have been observed in the functional architecture of the human brain with advancing age. However, functional connectivity (FC) is also a powerful feature to detect unique “connectome fingerprints,” allowing identification of individuals among their peers. Although fingerprinting has been robustly observed in samples of young adults, the reliability of this approach has not been demonstrated across the lifespan. We applied the fingerprinting framework to the Cambridge Centre for Ageing and Neuroscience cohort (n = 483 aged 18 to 89 years). We found that individuals are “fingerprintable” (i.e., identifiable) across independent functional MRI scans throughout the lifespan. We observed a U-shape distribution in the strength of “self-identifiability” (within-individual correlation across modalities), and “others-identifiability” (between-individual correlation across modalities), with a decrease from early adulthood into middle age, before improving in older age. FC edges contributing to self-identifiability were not restricted to specific brain networks and were different between individuals across the lifespan sample. Self-identifiability was additionally associated with regional brain volume. These findings indicate that individual participant-level identification is preserved across the lifespan despite the fact that its components are changing nonlinearly. MIT Press 2023-10-01 /pmc/articles/PMC10473304/ /pubmed/37781144 http://dx.doi.org/10.1162/netn_a_00320 Text en © 2023 Massachusetts Institute of Technology https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. For a full description of the license, please visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
St-Onge, Frédéric
Javanray, Mohammadali
Pichet Binette, Alexa
Strikwerda-Brown, Cherie
Remz, Jordana
Spreng, R. Nathan
Shafiei, Golia
Misic, Bratislav
Vachon-Presseau, Étienne
Villeneuve, Sylvia
Functional connectome fingerprinting across the lifespan
title Functional connectome fingerprinting across the lifespan
title_full Functional connectome fingerprinting across the lifespan
title_fullStr Functional connectome fingerprinting across the lifespan
title_full_unstemmed Functional connectome fingerprinting across the lifespan
title_short Functional connectome fingerprinting across the lifespan
title_sort functional connectome fingerprinting across the lifespan
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473304/
https://www.ncbi.nlm.nih.gov/pubmed/37781144
http://dx.doi.org/10.1162/netn_a_00320
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