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Inferring the heritability of large-scale functional networks with a multivariate ACE modeling approach
Recent evidence suggests that the human functional connectome is stable at different timescales and is unique. These characteristics posit the functional connectome not only as an individual marker but also as a powerful discriminatory measure characterized by high intersubject variability. Among di...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MIT Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233119/ https://www.ncbi.nlm.nih.gov/pubmed/34189376 http://dx.doi.org/10.1162/netn_a_00189 |
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author | Ribeiro, Fernanda L. dos Santos, Felipe R. C. Sato, João R. Pinaya, Walter H. L. Biazoli, Claudinei E. |
author_facet | Ribeiro, Fernanda L. dos Santos, Felipe R. C. Sato, João R. Pinaya, Walter H. L. Biazoli, Claudinei E. |
author_sort | Ribeiro, Fernanda L. |
collection | PubMed |
description | Recent evidence suggests that the human functional connectome is stable at different timescales and is unique. These characteristics posit the functional connectome not only as an individual marker but also as a powerful discriminatory measure characterized by high intersubject variability. Among distinct sources of intersubject variability, the long-term sources include functional patterns that emerge from genetic factors. Here, we sought to investigate the contribution of additive genetic factors to the variability of functional networks by determining the heritability of the connectivity strength in a multivariate fashion. First, we reproduced and extended the connectome fingerprinting analysis to the identification of twin pairs. Then, we estimated the heritability of functional networks by a multivariate ACE modeling approach with bootstrapping. Twin pairs were identified above chance level using connectome fingerprinting, with monozygotic twin identification accuracy equal to 57.2% on average for whole-brain connectome. Additionally, we found that a visual (0.37), the medial frontal (0.31), and the motor (0.30) functional networks were the most influenced by additive genetic factors. Our findings suggest that genetic factors not only partially determine intersubject variability of the functional connectome, such that twins can be identified using connectome fingerprinting, but also differentially influence connectivity strength in large-scale functional networks. |
format | Online Article Text |
id | pubmed-8233119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MIT Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-82331192021-06-28 Inferring the heritability of large-scale functional networks with a multivariate ACE modeling approach Ribeiro, Fernanda L. dos Santos, Felipe R. C. Sato, João R. Pinaya, Walter H. L. Biazoli, Claudinei E. Netw Neurosci Research Article Recent evidence suggests that the human functional connectome is stable at different timescales and is unique. These characteristics posit the functional connectome not only as an individual marker but also as a powerful discriminatory measure characterized by high intersubject variability. Among distinct sources of intersubject variability, the long-term sources include functional patterns that emerge from genetic factors. Here, we sought to investigate the contribution of additive genetic factors to the variability of functional networks by determining the heritability of the connectivity strength in a multivariate fashion. First, we reproduced and extended the connectome fingerprinting analysis to the identification of twin pairs. Then, we estimated the heritability of functional networks by a multivariate ACE modeling approach with bootstrapping. Twin pairs were identified above chance level using connectome fingerprinting, with monozygotic twin identification accuracy equal to 57.2% on average for whole-brain connectome. Additionally, we found that a visual (0.37), the medial frontal (0.31), and the motor (0.30) functional networks were the most influenced by additive genetic factors. Our findings suggest that genetic factors not only partially determine intersubject variability of the functional connectome, such that twins can be identified using connectome fingerprinting, but also differentially influence connectivity strength in large-scale functional networks. MIT Press 2021-06-03 /pmc/articles/PMC8233119/ /pubmed/34189376 http://dx.doi.org/10.1162/netn_a_00189 Text en © 2021 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/legalcode (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Ribeiro, Fernanda L. dos Santos, Felipe R. C. Sato, João R. Pinaya, Walter H. L. Biazoli, Claudinei E. Inferring the heritability of large-scale functional networks with a multivariate ACE modeling approach |
title | Inferring the heritability of large-scale functional networks with a multivariate ACE modeling approach |
title_full | Inferring the heritability of large-scale functional networks with a multivariate ACE modeling approach |
title_fullStr | Inferring the heritability of large-scale functional networks with a multivariate ACE modeling approach |
title_full_unstemmed | Inferring the heritability of large-scale functional networks with a multivariate ACE modeling approach |
title_short | Inferring the heritability of large-scale functional networks with a multivariate ACE modeling approach |
title_sort | inferring the heritability of large-scale functional networks with a multivariate ace modeling approach |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233119/ https://www.ncbi.nlm.nih.gov/pubmed/34189376 http://dx.doi.org/10.1162/netn_a_00189 |
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